sciex x500 qtof system user guide€¦ · replace the cds bottle ... import a library database...

SCIEX X500 QTOF System

System User Guide

August 2017RUO-IDV-05-2334-E

This document is provided to customers who have purchased SCIEX equipment to use in the operation of such SCIEXequipment. This document is copyright protected and any reproduction of this document or any part of this document isstrictly prohibited, except as SCIEX may authorize in writing.

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System User GuideSCIEX X500 QTOF SystemRUO-IDV-05-2334-E2 / 234

Chapter 1 Operational Precautions and Limitations................................................................................8General Safety Information................................................................................................................................................8Regulatory Compliance......................................................................................................................................................8

Australia and New Zealand..........................................................................................................................................8Canada........................................................................................................................................................................9Europe.........................................................................................................................................................................9United States...............................................................................................................................................................9International..............................................................................................................................................................10

Electrical Precautions.......................................................................................................................................................10AC Mains Supply........................................................................................................................................................10Protective Earth Conductor........................................................................................................................................11

Chemical Precautions.......................................................................................................................................................11System Safe Fluids.....................................................................................................................................................12

Ventilation Precautions....................................................................................................................................................13Environmental Precautions..............................................................................................................................................14

Electromagnetic Environment....................................................................................................................................15Decommissioning and Disposal..................................................................................................................................15

Equipment Use and Modification.....................................................................................................................................16Qualified Personnel..........................................................................................................................................................16Contact Us.......................................................................................................................................................................17Technical Support............................................................................................................................................................17Documentation Symbols and Conventions.......................................................................................................................17

Chapter 2 Principles of Operation............................................................................................................19System Overview..............................................................................................................................................................19Hardware Overview.........................................................................................................................................................20

Panel Symbols............................................................................................................................................................24Theory of Operation.........................................................................................................................................................24

Data Handling............................................................................................................................................................25Theory of Operation—SCIEX OS......................................................................................................................................25

Software Overview.....................................................................................................................................................25Scan Techniques........................................................................................................................................................25Quantitative Analysis.................................................................................................................................................28Integration.................................................................................................................................................................28Results Tables............................................................................................................................................................28Calibration Curves.....................................................................................................................................................28Regression Equations.................................................................................................................................................29Weighting Factors......................................................................................................................................................30Regression Types.......................................................................................................................................................30

SCIEX X500 QTOF SystemSystem User Guide3 / 234RUO-IDV-05-2334-E

Contents

Qualitative Analysis...................................................................................................................................................33

Chapter 3 Operating Instructions—Hardware........................................................................................36Start Up the System.........................................................................................................................................................36Shut Down and Vent the System......................................................................................................................................37Diverter Valve..................................................................................................................................................................38

Plumb the Diverter Valve in Injector Mode................................................................................................................39Plumb the Diverter Valve in Diverter Mode................................................................................................................40

Calibrant Delivery System................................................................................................................................................41Replace the CDS Bottle..............................................................................................................................................41Start the CDS.............................................................................................................................................................42Stop the CDS..............................................................................................................................................................42Flush the CDS.............................................................................................................................................................42

Chapter 4 Configure Devices....................................................................................................................45Add Devices.....................................................................................................................................................................45Edit Device Settings.........................................................................................................................................................45Delete Devices.................................................................................................................................................................46Deactivate Devices...........................................................................................................................................................46

Chapter 5 Configure Access to the Software..........................................................................................48Users Overview................................................................................................................................................................48

Roles and Permissions...............................................................................................................................................48Access to Analytics Features......................................................................................................................................50Add Users..................................................................................................................................................................53Deactivate a User.......................................................................................................................................................53Remove a User...........................................................................................................................................................54

Enable Full Screen Mode..................................................................................................................................................54Select Laboratory Information Management System (LIMS) Settings...............................................................................54Select Queue Options.......................................................................................................................................................54Select Regional Settings...................................................................................................................................................55Manage the Compound Libraries.....................................................................................................................................55

Import a LibraryView Package...................................................................................................................................55Import a Compound Database...................................................................................................................................56Import a Cliquid Package...........................................................................................................................................57Import an Excel File...................................................................................................................................................58Import a Library Database Snapshot .........................................................................................................................59Import a Library Package from a Third Party .............................................................................................................60Install a Licensed LibraryView Package......................................................................................................................60Compound Conflicts ..................................................................................................................................................62Add a Compound.......................................................................................................................................................64Add a Mass Spectrum to a Compound.......................................................................................................................64

Chapter 6 Operating Instructions—Software.........................................................................................66About the Home Page......................................................................................................................................................66About the Ribbon and Launcher......................................................................................................................................67About the Status Panel....................................................................................................................................................69

Add a Project.............................................................................................................................................................71Select a Project..........................................................................................................................................................72


Contents

Control the Device Status...........................................................................................................................................72Show the Status Panel...............................................................................................................................................72Hide the Status Panel.................................................................................................................................................72

Data Acquisition Panel.....................................................................................................................................................72User Workflows................................................................................................................................................................73

Analysts.....................................................................................................................................................................73Method Developers....................................................................................................................................................74Administrators...........................................................................................................................................................74Reviewers..................................................................................................................................................................74

Batch and Queue Workspaces.........................................................................................................................................74Manage the Batch.....................................................................................................................................................75Import a Batch ..........................................................................................................................................................76Import a Batch from the LIMS....................................................................................................................................77Create a Batch Manually............................................................................................................................................78Use the Plate Layout Feature to Create a Batch.........................................................................................................80Create an Ion Reference Table...................................................................................................................................82Calibrate the System Using the CDS..........................................................................................................................83Calibrate the System Using an LC Method.................................................................................................................83Equilibrate the System...............................................................................................................................................84Manage the Queue....................................................................................................................................................84Submit a Single Sample to the Queue........................................................................................................................86Submit Multiple Samples to the Queue......................................................................................................................86Show or Hide Columns...............................................................................................................................................87Add a Component Component Concentration Column..............................................................................................87Delete a Component Concentration Column..............................................................................................................87Queue Icons...............................................................................................................................................................88

MS Method Workspace....................................................................................................................................................88Create an MS Method................................................................................................................................................88MS Method Experiments............................................................................................................................................90About MS Methods....................................................................................................................................................91MS Method Parameters.............................................................................................................................................93Calculate the Dynamic Collision Energy for MS Methods.........................................................................................103

LC Method Workspace...................................................................................................................................................104Create an LC Method...............................................................................................................................................104

Explorer Workspace.......................................................................................................................................................104Verify the Presence of an Analyte............................................................................................................................104Extract Ions..............................................................................................................................................................105Open a Total Ion Chromatogram.............................................................................................................................108Open a Base Peak Chromatogram...........................................................................................................................110Show the Data and Peaks Table...............................................................................................................................112Show Sample Information........................................................................................................................................114Show the Graph Selection Information....................................................................................................................115Edit Settings in Graphs.............................................................................................................................................120Work with Data in Graphs.......................................................................................................................................122Use the Two-Pane Operation Tools..........................................................................................................................128Move Panes or Windows.........................................................................................................................................129Perform a Gaussian Smooth.....................................................................................................................................131


Contents

Threshold Data.........................................................................................................................................................132Subset Data (to Graph Selection).............................................................................................................................134Baseline Subtract Chromatogram............................................................................................................................135Offset Chromatogram..............................................................................................................................................137Centroid a Spectrum................................................................................................................................................138Export Data as Text..................................................................................................................................................140Export the Peak List as Text.....................................................................................................................................142Print Data.................................................................................................................................................................142Reset Options...........................................................................................................................................................143Set Options..............................................................................................................................................................143

Analytics Workspace......................................................................................................................................................147Set Project Secure Export Settings...........................................................................................................................147Enable Project Modified Peak Warning....................................................................................................................148Define the Project Default Settings..........................................................................................................................148Create a Processing Method....................................................................................................................................148About Results Tables...............................................................................................................................................150Review Peaks...........................................................................................................................................................169About Statistics Pane...............................................................................................................................................176Calibration Curve: Options.......................................................................................................................................179Analyzing Data Using Metric Plots...........................................................................................................................181Audit Trails...............................................................................................................................................................183

Integration Algorithm Parameters..................................................................................................................................186MQ4 Integration Algorithm Parameters...................................................................................................................186AutoPeak Integration Algorithm Parameters...........................................................................................................188

Edit Report Templates....................................................................................................................................................189Reporter Templates..................................................................................................................................................191

MS Tune.........................................................................................................................................................................192Perform a Quick Status Check..................................................................................................................................192Optimize the Detector..............................................................................................................................................193Tune Q1...................................................................................................................................................................194Tune TOF MS............................................................................................................................................................194Tune Q1 High...........................................................................................................................................................195Perform Advanced Troubleshooting.........................................................................................................................196Restore Instrument Data..........................................................................................................................................196

Event Log Workspace.....................................................................................................................................................197View Logs................................................................................................................................................................197Print Logs.................................................................................................................................................................197Archive Logs............................................................................................................................................................197

Chapter 7 Service and Maintenance Information.................................................................................199Recommended Maintenance Schedule..........................................................................................................................199Clean the Surfaces.........................................................................................................................................................201Clean the Front-End.......................................................................................................................................................201

Symptoms of Contamination....................................................................................................................................202Required Materials ..................................................................................................................................................202Cleaning Best Practices............................................................................................................................................203Prepare the Mass Spectrometer...............................................................................................................................205Clean the Curtain Plate............................................................................................................................................206


Contents

Clean the Front of the Orifice Plate..........................................................................................................................207Put the Mass Spectrometer Back in Service.............................................................................................................207

Empty the Source Exhaust Drain Bottle..........................................................................................................................207Replace the Check Valve and Flow Module...................................................................................................................210Inspect the Roughing Pump Oil Level............................................................................................................................211Storage and Handling....................................................................................................................................................212Move the Mass Spectrometer........................................................................................................................................213Generate a Support Package..........................................................................................................................................219

Chapter 8 Mass Spectrometer Troubleshooting...................................................................................220

Appendix A Recommended Calibration Ions........................................................................................223APCI Calibration Ions.....................................................................................................................................................223ESI Calibration Ions........................................................................................................................................................225

Appendix B Exact Masses and Chemical Formulas...............................................................................228

Appendix C Glossary of Symbols...........................................................................................................229

Appendix D Glossary of Warnings.........................................................................................................233


Contents

Note: Before operating the system, carefully read all of the sections of this guide.

This section contains general safety-related information and provides regulatory compliance information. It alsodescribes potential hazards and associated warnings for the system and the precautions that should be taken tominimize the hazards.

In addition to this section, refer to Glossary of Symbols on page 229 for information about the symbols andconventions used in the laboratory environment, on the system, and in this documentation. Refer to the SitePlanning Guide for site requirements, including AC mains supply, source exhaust, ventilation, compressed air,nitrogen, and roughing pump requirements.

General Safety InformationTo prevent personal injury or system damage, read, understand, and obey all of the safety precautions and warningsin this document, the manufacturer chemical safety data sheet (SDS), and product label information. These labelsare shown with internationally recognized symbols. Failure to heed these warnings could result in serious injury.

This safety information is intended to supplement federal, state, provincial, and local environmental health andsafety (EHS) regulations. The information provided covers system-related safety information applicable to theoperation of the system. It does not cover every safety procedure that should be practised. Ultimately, the userand the organization are responsible for compliance with federal, state, provincial, and local EHS regulations andfor maintaining a safe laboratory environment.

Refer to the appropriate laboratory reference material and standard operating procedures.

Regulatory ComplianceThis system complies with the regulations and standards listed in this section. Refer to the Declaration of Conformityincluded with the system and the individual system components for dated references. Applicable labels have beenaffixed to the system.

Australia and New Zealand• Electromagnetic Compatibility (EMC): Radio Communications Act 1992 as implemented in these

standards:

• Electromagnetic Interference—AS/NZS CISPR 11/ EN 55011/ CISPR 11 (Class A) . Refer to ElectromagneticInterference on page 15.


1Operational Precautions andLimitations

• Safety: AS/NZ 61010-1 and IEC 61010-2-061

Canada• Electromagnetic Interference (EMI): CAN/CSAA CISPR11. This ISM device complies with Canadian

ICES-001. Refer to Electromagnetic Interference on page 15.

• Safety:

• CAN/CSA C22.2 No. 61010-1

• CAN/CSA C22.2 No 61010-2-061

Europe• Electromagnetic Compatibility (EMC): Electromagnetic Compatibility directive 2014/30/EU as

implemented in these standards:

• EN 61326-1

• EN 55011 (Class A)Refer to Electromagnetic Compatibility on page 15.

• Safety: Low Voltage Directives 2014/35/EU as implemented in these standards:

• EN 61010-1

• EN 61010-2-061

• Waste Electrical and Electronic Equipment (WEEE): Waste Electrical and Electronic Equipment 2012/96/EEC, as implemented in EN 40519. Refer to Waste Electrical and Electronic Equipment on page 16.

• Packaging and Packaging Waste (PPW): Packaging and Packaging Waste Directive 94/62/EC

United States• Radio Emissions Interference Regulations: 47 CFR 15, as implemented in FCC Part 15 (Class A)

• Safety: Occupational Safety and Health Regulations, 29 CFR 1910, as implemented in these standards:

• UL 61010-1

• IEC 61010-2-061


Operational Precautions and Limitations

International• Electromagnetic Compatibility (EMC):

• IEC 61326-1

• IEC CISPR 11 (Class A)

• IEC 61000-3-2

• IEC 61000-3-3Refer to Electromagnetic Compatibility on page 15.

• Safety:

• IEC 61010-1

• IEC 61010-2-061

Electrical Precautions

WARNING! Electrical Shock Hazard. Do not remove the covers. Removing the coversmight cause injury or malfunctioning of the system. The covers need not be removedfor routine maintenance, inspection, or adjustment. Contact a SCIEX Field ServiceEmployee (FSE) for repairs that require the covers to be removed.

• Follow required electrical safe work practices.

• Use cable management practices to control electrical cables. This will reduce the chance of a tripping hazard.

For information about system electrical specifications, refer to the Site Planning Guide.

AC Mains SupplyConnect the system to a compatible AC mains supply as instructed in this guide.

WARNING! Electrical Shock Hazard. Use only qualified personnel for the installationof all of the electrical supplies and fixtures, and make sure that all of the installationsadhere to local regulations and safety standards.

WARNING! Electrical Shock Hazard. Make sure that the system can be disconnectedfrom the mains supply outlet in an emergency. Do not block the mains supply outlet.



WARNING! Electrical Shock Hazard. Use only the power cables supplied with thesystem. Do not use power cables that are not properly rated for the operation ofthis system.

An external line transformer is not needed for the mass spectrometer or roughing pump.

Protective Earth ConductorThe mains supply must include a correctly installed protective earth conductor. The protective earth conductormust be installed or checked by a qualified electrician before the system is connected.

WARNING! Electrical Shock Hazard. Do not intentionally interrupt the protectiveearth conductor. Any interruption of the protective earth conductor creates anelectrical shock hazard.

WARNING! Electrical Shock Hazard. Make sure that a protective earth conductor(grounding cable) is connected between the sample loop and an appropriategrounding point at the ion source. This supplementary grounding will reinforce thesafety configuration specified by SCIEX.

Chemical Precautions

WARNING! Radiation Hazard, Biohazard, or Toxic Chemical Hazard. Determinewhether decontamination is required prior to cleaning or maintenance. Thecustomer must decontaminate the system prior to cleaning or maintenanceif radioactive materials, biological agents, or toxic chemicals have been usedwith the system.

WARNING! Environmental Hazard. Do not dispose of system components in municipalwaste. Follow local regulations when disposing of components.

WARNING! Biohazard, Toxic Chemical Hazard. Connect the drain tubing tothe mass spectrometer and the source exhaust drain bottle properly, toprevent leaks.

• Determine which chemicals have been used in the system prior to service and regular maintenance. Refer tothe Safety Data Sheets for the health and safety precautions that must be followed with chemicals.



• Work in a well-ventilated area or fume hood.

• Always wear assigned personal protective equipment, including powder-free neoprene or nitrile gloves, safetyglasses, and a laboratory coat.

• Avoid ignition sources when working with flammable materials, such as isopropanol, methanol, and otherflammable solvents.

• Take care in the use and disposal of any chemicals. Potential risk of personal injury if proper procedures forhandling and disposing of chemicals are not followed.

• Avoid skin contact with chemicals during cleaning and wash hands after use.

• Make sure that all exhaust hoses are connected properly and that all connections are functioning as designed.

• Collect all spent liquids and dispose of them as hazardous waste.

• Comply with all of the local regulations for the storage, handling, and disposal of biohazardous, toxic, orradioactive materials.

• (Recommended) Use secondary containment trays beneath the roughing pump, the solvent bottles, and thewaste collection container to capture potential chemical spills.

System Safe FluidsThe following fluids can safely be used with the system. Refer to Required Materials on page 202 for informationabout safe cleaning solutions.

CAUTION: Potential System Damage. Do not use any other fluid until confirmation isreceived from SCIEX that it does not present a hazard. This is not an exhaustive list.

• Organic Solvents

• MS-grade acetonitrile; up to 100%

• MS-grade methanol; up to 100%

• Isopropanol; up to 100%

• HPLC-grade or higher water; up to 100%

• Tetrahydrofuran; up to 100%

• Toluene and other aromatic solvents; up to 100%

• Hexanes; up to 100%



• Buffers

• Ammonium acetate; less than 1%

• Ammonium formate; less than 1%

• Phosphate; less than 1%

• Acids and Bases

• Formic acid; less than 1%

• Acetic acid; less than 1%

• Trifluoroacetic acid (TFA); less than 1%

• Heptafluorobutyric acid (HFBA); less than 1%

• Ammonia/ammonium hydroxide; less than 1%

• Phosphoric acid; less than 1%

• Trimethylamine; less than 1%

• Triethylamine; less than 1%

Ventilation PrecautionsThe venting of fumes and disposal of waste must comply with all of the federal, state, provincial, and local healthand safety regulations. It is the responsibility of the customer to make sure that the air quality is maintained incompliance with local health and safety regulations.

The source exhaust system and roughing pump must be vented to a dedicated laboratory fume hood or an externalexhaust system.

WARNING! Fire Hazard. Make sure that the source exhaust system is connected andfunctioning to prevent flammable vapor from accumulating in the ion source.

WARNING! Radiation Hazard, Biohazard, or Toxic Chemical Hazard. Take careto vent exhaust gases to a dedicated laboratory fume hood or exhaust systemand make sure that the ventilation tubing is secured with clamps. Make surethat the laboratory has appropriate air exchange for the work performed.



WARNING! Radiation Hazard, Biohazard, or Toxic Chemical Hazard. Do notoperate the mass spectrometer if the source exhaust drain and roughingpump exhaust hoses are not properly connected to the laboratory ventilationsystem. Perform a regular check of the exhaust tubing to make sure thatthere are no leaks. The use of mass spectrometers without proper systemventilation might constitute a health hazard and might result in serious injury.

WARNING! Radiation Hazard, Biohazard, or Toxic Chemical Hazard. Use theion source only if you have knowledge of and training in the proper use,containment, and evacuation of toxic or injurious materials used with theion source.

WARNING! Puncture Hazard, Radiation Hazard, Biohazard, or Toxic ChemicalHazard. Discontinue use of the ion source if the ion source window is crackedor broken and then contact a SCIEX Field Service Employee (FSE). Any toxicor injurious materials introduced into the equipment will be present in thesource exhaust output. Dispose of sharps following established laboratorysafety procedures.

Environmental PrecautionsUse qualified personnel for the installation of electrical mains, heating, ventilation, and plumbing supplies andfixtures. Make sure that all of the installations comply with local bylaws and biohazard regulations. For informationabout the required environmental conditions for the system, refer to the Site Planning Guide.

Allow access space around the equipment when setting up the system.

DANGER! Explosion Hazard. Do not operate the system in an environment containingexplosive gases. The system is not designed for operation in an explosiveenvironment.

WARNING! Biohazard. For biohazardous material use, always comply with localregulations for hazard assessment, control, and handling. This system or any partis not intended to act as a biological containment.

CAUTION: Potential Mass Shift. Maintain a stable ambient temperature. If the temperaturechanges by more than 2 °C per hour, then the resolution and mass calibration might beaffected.



Electromagnetic Environment

Electromagnetic Compatibility

Basic Electromagnetic Environment: Environment existing at locations characterized by being supplieddirectly at low voltage from the public mains network.

Performance Criteria A (Criteria A): Equipment shall operate as intended with no degradation of performanceand no loss of function during or after test.

Performance Criteria B (Criteria B): Equipment may experience loss of function (one or more) during testbut shall operate as intended with some degradation of performance and functions self-recoverable after test.

Performance Criteria C (Criteria C): Equipment may experience loss of function (one or more) during testbut shall operate as intended with some degradation of performance and functions recoverable by operator aftertest.

The equipment is intended for use in a basic electromagnetic environment.

The expected performance loss under the electromagnetic immunity conditions is less than 20% change in totalion count (TIC).

Make sure that a compatible electromagnetic environment for the equipment can be maintained so that the devicewill perform as intended. If the power supply line is subject to high electrical noise, then install a surge protector.

Electromagnetic Interference

Class A Equipment: Equipment which is suitable for use in all establishments other than domestic and thosedirectly connected to a low voltage power supply network which supplies buildings used for domestic purposes.[Derived from CISPR 11:2009, 5.3] Class A equipment shall meet Class A limits.

This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to Part15 of the FCC (Federal Communications Commission) Compliance Rules.

These limits are designed to provide reasonable protection against harmful interference when the equipment isoperated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energyand, if not installed and used in accordance with the operator's manual, can cause harmful interference to radiocommunications.

Operation of this equipment in a residential area is likely to cause harmful interference in which case you will berequired to correct the interference, at your own expense. Changes or modifications not expressly approved bythe manufacturer could void your authority to operate the equipment.

Decommissioning and DisposalBefore decommissioning, decontaminate the entire system following local regulations.

When removing the system from service, separate and recycle different materials according to national and localenvironmental regulations. Refer to Storage and Handling on page 212.



Note: SCIEX will not accept any system returns without a completed Decontamination Form. Contact an FSEto obtain a copy of the form.

Do not dispose of system components or subassemblies, including computer parts, as unsorted municipal waste.

Waste Electrical and Electronic Equipment

Follow local municipal waste ordinances for proper disposal provisions to reduce the environmental impact ofwaste, electrical, and electronic equipment (WEEE). To safely dispose of this equipment, contact a local CustomerService office for complimentary equipment pick-up and recycling.

Equipment Use and Modification

WARNING! Personal Injury Hazard. Contact the SCIEX representative if productinstallation, adjustment, or relocation is required.


WARNING! Personal Injury Hazard. Use SCIEX-recommended parts only. Use of partsnot recommended by SCIEX or use of parts for any purpose other than their intendedpurpose can put the user at risk of harm or negatively impact system performance.

Use the system indoors in a laboratory that complies with the environmental conditions recommended in the SitePlanning Guide.

If the system is used in an environment or in a manner not prescribed by the manufacturer, then the protectionprovided by the equipment might be impaired.

Unauthorized modification or operation of the system might cause personal injury and equipment damage, andmight void the warranty. Erroneous data might be generated if the system is operated either above or below therecommended environmental conditions or operated with unauthorized modifications. Contact an FSE for informationon servicing the system.

Qualified PersonnelOnly qualified SCIEX personnel shall install, inspect, and service the equipment. After installing the system, theField Service Employee (FSE) uses the Customer Familiarization Checklist to orient the customer on systemoperation, cleaning, and basic maintenance.



Only personnel qualified by the manufacturer shall maintain the equipment. A laboratory designate can befamiliarized with the Qualified Maintenance Person (QMP) procedures during the installation. A QMP is a personwho is suitably aware of the electrical and chemical risks associated with servicing laboratory equipment.

Contact UsSCIEX Support

• sciex.com/contact-us

• sciex.com/request-support

Customer Training

• In North America: [email protected]

• In Europe: [email protected]

• Outside the EU and North America, visit sciex.com/education for contact information.

Online Learning Center

• SCIEXUniversity

For the latest guidance on cybersecurity for SCIEX products, visit sciex.com/productsecurity.

Technical SupportSCIEX and its representatives maintain a staff of fully-trained service and technical specialists located throughoutthe world. They can answer questions about the system or any technical issues that might arise. For moreinformation, visit the SCIEX website at sciex.com.

Documentation Symbols and ConventionsThe following symbols and conventions are used throughout the guide.

DANGER! Danger signifies an action which leads to severe injury or death.

WARNING! Warning signifies an action that could cause personal injury if precautionsare not followed.



https://sciex.com/contact-us

https://sciex.com/request-support

mailto:[email protected]

mailto:[email protected]

https://sciex.com/education

https://training.sciex.com

https://sciex.com/productsecurity

https://sciex.com

CAUTION: Caution signifies an operation that could cause damage to the system orcorruption or loss of data if precautions are not followed.

Note: Note emphasizes significant information in a procedure or description.

Tip! Tip provides useful information that helps apply the techniques and procedures in the text for a specificneed and provides shortcuts, but is not essential to the completion of a procedure.



The SCIEX X500 QTOF system is designed for the qualitative and quantitative analysis of chemical species.

This section includes information about the mass spectrometer and the SCIEX OS. Refer to the ion source OperatorGuide for an overview of the ion source.

System OverviewThe SCIEX X500 QTOF system includes the following components:

• A SCIEX X500 QTOF mass spectrometer with a roughing pump.

• A Turbo VTM ion source that uses either the twin ESI probe or the twin atmospheric pressure chemical ionization(APCI) probe. Refer to the Turbo VTM Ion Source Operator Guide.

• A SCIEX-supplied computer and monitor with the SCIEX OS for instrument optimization, acquisition methoddevelopment, processing, and data acquisition. For computer specifications and requirements, refer to theRelease Notes for the SCIEX OS.


2Principles of Operation

Hardware Overview

Figure 2-1 Front and Right Side View: X500R


Principles of Operation

Figure 2-2 Front and Right Side View: X500B

DescriptionItem

Diverter valve in standard location. Refer to Diverter Valve on page 381

Alternate (left) location for diverter valve. For more information, contact an FSE.2

Ion source. Refer to the ion source Operator Guide.3

Calibrant bottles. Refer to Replace the CDS Bottle on page 41.4

Panel symbols. Refer to Panel Symbols on page 24.5



Figure 2-3 Back and Left Side View: X500R



Figure 2-4 Back and Left Side View: X500B

DescriptionItem

Left bulkhead. Contains the gas and communication connections.1

Vent button. Refer to Shut Down and Vent the System on page 37.2

Sources connection. Some ion sources connect to this port.3

AUX IO connection. Not used.4

Ethernet connection. Used for communication with the acquisition computer.5

Zero air gas supply6

Exhaust waste. Refer to Empty the Source Exhaust Drain Bottle on page 207.7

Nitrogen gas supply8

Exhaust gas supply. The air supply for the ion source.9



DescriptionItem

Vacuum hose connection for the roughing pump10

Mass spectrometer convenience switch. Refer to Start Up the System on page 36 or ShutDown and Vent the System on page 37.

11

Location of Infiniband cable connection to the TDC card in the acquisition computer12

Panel SymbolsTable 2-1 describes the mass spectrometer status LEDs.

Table 2-1 Panel Symbols

DescriptionNameColorLED

Lit when the system is powered up.PowerGreen

Lit when the correct vacuum level has beenachieved. Flashing if the vacuum is not at thecorrect level (during pump down and venting).

VacuumGreen

Lit when the system is in the Ready state. Thesystem must be in the Ready state to operate.

ReadyGreen

Flashing when the system is acquiring data.ScanningBlue

Lit when the system encounters a system fault.FaultRed

After the system is turned on, the power LED illuminates, and the fault LED flashes for a few seconds. Then thevacuum LED begins to flash. After the correct vacuum level is achieved, this LED remains lit.

Theory of OperationMass spectrometry measures the mass-to-charge ratio of ions to identify and quantify compounds.

The SCIEX X500 QTOF system has a series of quadrupole filters that transmit ions according to their mass-to-charge(m/z) value. The first quadrupole in this series is the QJet

® ion guide, which is located between the orifice plate

and the Q0 region. The QJet® ion guide does not filter ions, but focuses them before they enter the Q0 region. By

prefocusing the larger ion flux created by the wider orifice, the QJet® ion guide increases instrument sensitivity



and improves the signal-to-noise ratio. In the Q0 region, the ions are again focused before passing into the Q1quadrupole.

The Q1 quadrupole sorts the ions before they enter the Q2 collision cell. The Q1 quadrupole works in two operationalmodes:

• Passing all ions within a specified m/z range to the Q2 collision cell. This is a TOF MS scan. All ions are analyzedby the TOF system.

• Passing one ion with a specified m/z ratio to the Q2 collision cell. This is a TOF MS/MS scan. Only the selectedion is analyzed.

In the Q2 collision cell, the internal energy of the ions is increased though collisions with gas molecules to thepoint that molecular bonds break, creating product ions. This technique allows users to design experiments thatmeasure the m/z ratio of product ions to determine the composition of the parent ions and to provide informationabout the structural and chemical properties of the molecules.

After passing through the Q2 collision cell, the ions enter the TOF region for additional mass analysis. They reachthe detector at different times depending on their m/z ratio. In the detector, the ions create a current that isconverted into a voltage pulse. These voltage pulses are counted and the number of pulses is directly proportionalto the quantity of ions entering the detector. The mass spectrometer converts the voltage pulses to a signal andthen correlates the signal to the time it takes each ion to reach the detector. The signal represents the ion intensityand the time to reach the detector represents a specific m/z value. The mass spectrometer shows this data as amass spectrum.

Data HandlingThe SCIEX OS requires a computer running the Windows 7, 64-bit operating system. The computer and theassociated system software work with the system controller and the associated firmware to control the systemand data acquisition. During system operation, the acquired data is sent to the SCIEX OS where it can be shownas either full mass spectra, intensity of single or multiple ions over time, or total ion current over time.

Theory of Operation—SCIEX OS

Software OverviewSCIEX OS contains instrument control, data acquisition, data processing, and reporting functionality, all in the onepackage.

Scan TechniquesThe system is a versatile and reliable system for performing liquid chromatography mass spectrometry analysison liquid sample streams to identify, quantify, and examine compounds.

The system uses the following mass spectrometry techniques to analyze samples:



• Two modes of single mass spectrometry (MS):

• Quadrupole-based single mass spectrometry (for Q1 calibration only)

• Time-of-flight-based single mass spectrometry

• One mode of tandem mass spectrometry (MS/MS):

• Product ion mass spectrometry

Different Data Views

The following figures show examples of two types of data views: total ion chromatogram (TIC) and extracted ionchromatogram (XIC).

TIC: The plot of the total ion current as a function of time.

Figure 2-5 Example TIC

XIC: An ion chromatogram created by taking intensity values at a single, discrete mass value or a mass range,from a series of mass spectral scans. It indicates the behavior of a given mass or mass range as a function of time.



Figure 2-6 Example XIC

Chromatograms

A chromatogram shows the variation of some quantity with respect to time in a repetitive experiment, for example,when the instrument is programmed to repeat a given set of mass spectral scans several times. Chromatographicdata is contiguous, even if the intensity of the data is zero. Chromatograms are not generated directly by theinstrument, but are generated from mass spectra.

In the chromatogram graph, the intensity, in counts per second (cps), is shown on the y-axis versus time on thex-axis. Peaks are automatically labeled.

In the case of LC-MS, the chromatogram is often shown as a function of time, the time at which a particular scanwas obtained, which can be derived from the scan number.

A chromatogram provides a general view of the data, usually time dependent when using an LC column, but itdoes provide information about the components of a peak. For example, while a chromatogram might show onlyone peak, that peak can represent more than one compound. That is, different masses.

Chromatographic data can change in both time and intensity if there is a change in the chromatographic conditionsin a given sample.

Spectra

A spectrum is the data that is obtained directly from the instrument and normally represents the number of ionsdetected with particular mass-to-charge (m/z) values. It is displayed as a graph with the m/z values on the x-axisand intensity (cps) represented on the y-axis.



For MS/MS data, the intensity is associated with all masses, precursor, and fragment ions.

When data is viewed as a spectrum, mass-specific information about a compound is obtained. A spectrum looksat a particular peak and provides m/z values of the corresponding compound, which can be used to find morespecific information. For example, a spectrum shows all of the masses that make up a peak, including the intensityof each mass.

Spectral intensities may change, but the masses are fixed because the mass of a compound does not change.

There are two ways to generate spectral data:

• If only one scan is acquired, then the data is shown as a spectrum.

• From a chromatogram.

A typical spectrum is shown with the molecular weight, labeled with the m/z (mass-to-charge ratio), on the x-axis.The intensity is shown on the y-axis.

Quantitative AnalysisQuantitative analysis is used to find the concentration of a specific substance in a sample. By analyzing an unknownsample and comparing it to other samples containing the same substance with known concentrations (standards),the software can calculate the concentration of the unknown sample. The process involves creating a calibrationcurve using the standards and then calculating the concentration for the unknown sample. The calculatedconcentrations of each sample are then available in a Results Table.

IntegrationIn LC-MS/MS data, integration refers to obtaining the area under a curve for the peak associated with a specificcompound. Through the development of a processing method which specifies the mass transitions, expectedretention times, internal standards, integration, and regression parameters, the software is able to automaticallyintegrate peaks for a given set of samples.

The compilation of quantitative or qualitative information for a given set of samples is called a Results Table. Referto Results Tables on page 28.

Results TablesA Results Table is a compilation of the quantitative and qualitative information associated with a set of samples.It includes, among others, the calculations for concentration and accuracy determined as a result of interpolatingthe calibration (standard) curve. The library search results, formula finding results, and other qualitative analysisresults are also available in the Results Table. Area, height, and other numerical characteristics can be shown. Thenumber and type of columns in the Results Tables can be edited for simplified viewing.

Calibration CurvesA calibration curve, also know as a standard concentration curve, is a method for determining the concentrationof a substance in an unknown sample by comparing the unknown sample to a set of standard samples of known



concentration. The calibration curve is a plot of how the instrument responds (the analytical signal) to changes inthe concentration of the analyte (the substance to be measured). The operator prepares a series of standardsacross a range of concentrations near the expected concentration of the analyte in the unknown sample.

Calibration standards are used to build calibration curves. Incorrect readings or missing readings on some of thecalibration samples might indicate issues with the analytical run. Follow acceptable methods found in literatureand regulatory agency guidances to create a calibration curve. Examples of good practice in the preparation ofcalibration curves include:

• Preparing calibration standards in blank matrix in which the analyte is to be measured.

• Generating a calibration curve for each analyte to be measured.

• Making sure of the coverage of the expected concentration range of the analyte, including typical and atypicalspecimens.

• Using six to eight standards to generate the curve.

This is not a comprehensive list and other guidances should be used in determining the best practice in developinga calibration curve for the laboratory.

Note: In some analytical runs, single-point calibration standards are used. Single-point calibrations are performedusing a matrix blank sample and a single standard concentration. The relationship between instrument responseand analyte concentration is determined by the line created by these two points. Both the acquisition andprocessing methods should be validated before being accepted for their intended use.

Regression EquationsThis section describes the equations used to calculate the regression curves. In the following equations, x representsthe analyte concentration for Standard samples and y represents the corresponding peak area or height. Theexact variables used for the regression depend on whether an internal standard is being used and whether thepeak area or the peak height is used as shown in Table 2-2.

Table 2-2 Regression Variables

yxArea Used?InternalStandard Used?

Aa / AisCa / Cis / DFYesYes

Ha / HisCa / Cis / DFNoYes

AaCa/ DFYesNo

HaCa/ DFNoNo

where:



• Ca = actual analyte concentration

• Cis = internal standard concentration

• DF = dilution factor

• Aa = analyte peak area

• Ais = internal standard peak area

• Ha = analyte peak height

• His = internal standard peak height

Weighting FactorsTable 2-3 shows how the weighting factor (w in the equations) is calculated for each of the seven weighting types.

Table 2-3 Weighting Factors

Weight (w)Weighting Type

Always 1.0.None

If |x| < 10-5, then w = 105. Otherwise, w = 1 / |x|.1 / x

If |x| < 10-5, then w = 1010. Otherwise, w = 1 / x2.1 / x2

If |y| < 10-8, then w = 108. Otherwise, w = 1 / |y|.1 / y

If |y| < 10-8, then w = 1016. Otherwise, w = 1 / y2.1 / y2

If x < 0, then an error is generated. If x < 10-5, then w = ln 105. Otherwise, w =|ln x|.

ln x

If y < 0, then an error is generated. If y < 10-8, then w = ln 108. Otherwise, w =|ln y|.

ln y

Regression TypesThe area of the analyte peaks in the calibration curve standards is plotted against the known concentrations.Subsequently, a line is fitted to the points. This regression line is used to calculate the concentration of the unknownsamples.

In the Analytics workspace, the following types of regression are available for the calibration curve:

• Linear (y = mx + b)

• Linear through Zero (y = mx)

• Mean Response Factor



• Quadratic (y = a2 + bx + c)

• Power

• Wagner

• Hill

As well, it is possible to add different types of weighting for the regression, including:

• None

• 1/x

• 1/x2

• 1/y

• 1/y2

• ln(x)

• ln(y)

Linear

The linear calibration equation is:

y = mx + b

The slope and intercept are calculated as:

where:

Linear Through Zero

The linear through zero calibration equation is:

y = mx

The slope is calculated as:

Mean Response Factor

The mean response factor calibration is:



y = mx

This is the same equation as for the linear though zero case. However, the slope is calculated differently as:

and the standard deviation of the response factor as:

where:

Note: Points whose x value is zero are excluded from the sums.

If there is some linearity and some curvature in the line of points, then use power regression instead of linear orquadratic regression to produce a line somewhere between these fits.

Quadratic

The quadratic calibration equation is:

y = a2x2 + a1x + a0

The polynomial co-efficients are calculated as:

a2 = (b2/b0 - b5/b3) / (b1/b0 - b4/b3)

a1 = b5/b3 - a2b4/b3

where:



Power

The power function calibration equation is:

y = axp

The equations for the linear calibration are used as described above to calculate the slope (m) and intercept (b),except that x in those equations is replaced by ln x and y is replaced by ln y. When this is done, a and p arecalculated as:

a = eb

p = m

If any of the x or y values are negative or zero, then an error is reported.

Wagner

The Wagner calibration equation is:

ln y = a2 (ln x)2 + a1 (ln x) + a0

The equations for the quadratic calibration are used as described above to calculate a0, a1, and a2, except that xin those equations is replaced by ln x and y is replaced by ln y.

If any of the x or y values are negative or zero, then an error is reported.

Hill

The Hill calibration equation is:

y = (a + bxn) / (c + xn)

It is not possible to provide an analytical function for solving for a, b, c, and n. Instead, the co-efficients aredetermined using the iterative Levenberg-Marquardt method.

Qualitative AnalysisQualitative analysis is the identification of a target or unknown compound. In mass spectrometry, determiningwhich compound is present is accomplished using mass accuracy, retention time, isotope pattern, library searching,and formula finding. Using all of these tools together can increase the confidence in identifying both targeted andnon-targeted compounds in unknown samples.

Mass Accuracy

When trying to identify a known target compound in a sample, it is useful to look at the mass accuracy of thatcompound and determine if a potential 'hit' for that compound has a mass accuracy within a certain tolerance.For example, imazalil has a chemical formula of C14H14Cl2N2O, which gives it a mass of 296.0483, to four decimalplaces. A protonated adduct is an ion with a positive charge that is normally detected using an accurate masstime-of-flight instrument. The protonated adduct of imazalil has a mass 297.0556. If it is suspected that imazalilis in a sample, then compare the mass of the compound found to the mass of the protonated imazalil and determine



how close the masses are. The closer those compounds match (ppm or Da), the more likely it is that the targetcompound is a match.

Retention Time

Most accurate mass spectrometry systems use some type of chromatography. The SCIEX X500 QTOF System usesliquid chromatography (LC). A set retention time using a known standard for the compound on the LC system isused to identify a known target compound in a sample. If the suspected compound is in an unknown sample, thenthe closer the retention time is to the set retention time from the standard, the more likely the unknown compoundcan be identified. Retention times can change and must be updated.

Isotope Pattern

The full scan mass spectrum from a compound on an accurate mass system has a distinct isotope pattern basedon its molecular formula. Figure 2-7 shows the isotope pattern for imazalil.

Figure 2-7 Isotope Pattern

Library Searching

Comparing acquired MS/MS spectra from unknown samples to a database of compounds with reference spectrais one of the most powerful tools in qualitative analysis. Library search algorithms compare the unknown spectrafrom the sample and then try to match the spectra to the known compounds and spectra in the database. Thecloser the match and the higher the reported score are, the more likely it is that the compound was identified.

The purity, fit and reverse fit are calculated as follows:

• If there is a peak at a given mass in both the (reduced) library spectrum and the (reduced) unknown spectrumwhose intensity ratio is within the limits specified by the user, the intensity of the peak in the library spectrumis set equal to that of the unknown spectrum



• The purity is calculated as:100.0 (ULtotal)

2 / (Utotal•Ltotal) where:

Utotal = ∑ Um•Um

Ltotal = ∑ Lm•Lm

ULtotal = ∑ Um•Lm

The sums include all masses where the intensities Um and Lm are the square roots of the mass-weighted, thatis reduced; unknown; and library entries. The purity is guaranteed to fall in the range between 0 to 100 andis a measure of the similarity of the library spectrum and the unknown spectrum.

• The fit is calculated in exactly the same manner as the purity, except that only masses which occur in the libraryspectrum are included in the sums. This has no effect on Ltotal or ULtotal because no terms are deleted fromthese sums. The fit is a measure of the degree to which the library spectrum is contained in the unknownspectrum. A high fit and a low purity indicates that the unknown spectrum is likely impure, but contains thelibrary compound.

• The reverse fit is also calculated in the same manner as the purity, except that only masses that occur in theunknown spectrum are included in the sums. The reverse fit is a measure of the degree to which the unknownspectrum is contained in the library spectrum.

Formula Finding

Using an accurate mass number, the formula finding algorithm tries to predict the possible chemical formula forthe compound, based on the MS and MS/MS spectrum generated from an accurate mass, mass spectrometer. Itis important to know that a high formula finder score does not necessarily mean that the compound in the sampleis the one identified by formula finder as there are often several formula that match within a few ppm of masserror. Care must be taken and other confirmatory testing must be done before a compound is identified usingformula finding.

A list of possible formula is determined using precursor mass accuracy, isotopic pattern, and MS/MS fragmentation.Proposed formulas are scored based on precursor mass accuracy and average MS/MS mass accuracy of matchingfragments.



WARNING! Personal Injury Hazard. Follow the instructions in the documentationwhen using the system. The protection provided by the equipment might be impairedif the equipment is used in a manner not specified by SCIEX.

Start Up the System

WARNING! Electrical Shock Hazard. Make sure that the system can be disconnectedfrom the mains supply outlet in an emergency. Do not block the mains supply outlet.

Note: Before operating the instrument, read the safety information in Operational Precautions and Limitationson page 8.

Prerequisites

• The site requirements specified in the Site Planning Guide are met. The Site Planning Guide includesinformation on the mains supply and connections, compressed air, nitrogen, roughing pump, ventilation,exhaust, and site clearance requirements. Contact us for a copy of the Site Planning Guide, if required.For contact information, go to sciex.com/contact-us

• The source exhaust gas, compressed air, and nitrogen gases are connected to the mass spectrometer.

• The 4 L source exhaust drain bottle is connected to the exhaust waste connection on the back of the massspectrometer and to the laboratory ventilation system.

• The source exhaust hoses are securely clamped at the mass spectrometer, drain bottle, and ventilationconnections.

• The mass spectrometer convenience switch is turned off and the mains supply cable is plugged into the massspectrometer.

• The mass spectrometer and roughing pump mains supply cables are plugged into the 200 VAC to 240 VACmains supply.

1. Turn on the roughing pump.

The On/Off switch is beside the mains supply input connection on the roughing pump.


3Operating Instructions—Hardware


Figure 3-1 Roughing Pump—On/Off Switch

2. Turn on the mass spectrometer convenience switch. Refer to Figure 2-3 or Figure 2-4.

3. Turn on the computer.

4. Open the SCIEX OS software.

Shut Down and Vent the SystemSome procedures require that the system be shut down. Others require that it also be vented. Follow these stepsto shut down and, if required, vent the system.

Note: If the input gas supply must be disconnected, then relieve the pressure in the gas lines before disconnectingit.

Tip! If the mass spectrometer will not be used for a length of time, then leave it in Standby mode with the ionsource in place. If the mass spectrometer must be shut down, then follow these instructions. Do not turn off theroughing pump until after the turbo pumps have spun down.

1. Complete or stop any ongoing scans.

CAUTION: Potential System Damage. Turn off the sample flow before shutting downthe system.

2. Turn off the sample flow to the system.


Operating Instructions—Hardware

3. In the SCIEX OS software, deactivate the devices, if they are active.

4. Close the software.

5. (If required) Follow these steps to vent the system:

Note: Vent the system before performing a full cleaning of the vacuum interface, before cleaning the Q0region, and before replacing the roughing pump oil. For more information contact the Qualified MaintenancePerson (QMP) or FSE.

a. Press and hold the Vent button for three seconds.

The Vacuum LED begins flashing quickly (more quickly than during pump down). The turbo pump spinsdown gradually.

b. Turn off the roughing pump. Allow the system to vent for 20 minutes.

6. Turn off the mass spectrometer convenience switch. Refer to Figure 2-3 on page 22 or Figure 2-4 on page 23.

7. Disconnect the mass spectrometer mains supply cable from the mains supply outlet.

8. (If venting the system) Disconnect the roughing pump mains supply cable from the mains supply outlet.

9. If the mass spectrometer will be vented and out of service for more than eight hours, then turn off the nitrogengas supply.

Unless the gas supply is turned off, nitrogen gas will continue to flow through the curtain plate at a rate of 4L/min when the instrument is shut down and vented.

After Venting the Mass Spectrometer• Perform a Quick Status Check on page 192.

• If resolution drift occurs 16 to 24 hours after startup, then perform a quick status check again.

Diverter ValveThe diverter valve is a two-position, six-port valve. It can be plumbed in injector mode or diverter mode. In injectormode, it can be configured with a sample loop for sample injection. In diverter mode, it can be configured to divertsample to waste at the beginning of each LC run.

CAUTION: Potential Wrong Result. Do not press the diverter valve button during a run.Doing so might result in incorrect data.



Plumb the Diverter Valve in Injector ModeWhen the valve is in Position A, the sample flows through the external loop. When the valve switches to PositionB, the sample is injected.

• Plumb the valve for injector mode.

Figure 3-2 Diverter Valve—Injector Mode Position A

Figure 3-3 Diverter Valve—Injector Mode Position B



DescriptionItem

Sample in1

Waste out2

Sample loop (ports 3 and 6)3

Mobile phase in4

To column (or to the mass spectrometer, if a column is not installed)5

Plumb the Diverter Valve in Diverter ModeWhen the valve is in Position A, the flow goes to waste. When the valve switches to Position B, the flow goes tothe mass spectrometer.

• Plumb the valve for diverter mode.

Figure 3-4 Diverter Valve—Diverter Mode Position A



Figure 3-5 Diverter Valve—Diverter Mode Position B

DescriptionItem

To mass spectrometer1

From column2

Waste out3

Calibrant Delivery SystemThe calibrant delivery system (CDS) introduces calibration solution for automated mass calibration of the massspectrometer, to ensure that the mass accuracy of the system is maintained throughout batch acquisition.

Because calibration takes about a minute and a half, we recommend frequent calibration.

Replace the CDS Bottle

WARNING! Toxic Chemical Hazard. Refer to the chemical product Safety Data Sheetsand follow all of the recommended safety procedures when handling, storing, anddisposing of chemicals. For health and safety precautions, refer to ChemicalPrecautions on page 11.

The CDS supports up to two bottles of calibrant. Use bottle one for the positive calibrant solution. Use bottle twofor the negative calibrant solution. Be sure to install the bottle in the correct position to avoid cross-contamination.



1. Turn the bottle counter-clockwise to remove it from the CDS.

2. Turn the new bottle clockwise to install it.

Start the CDSUse the direct control function to start the CDS manually when flushing the CDS or when introducing solutionsduring tuning.

1. On the status panel, click the Direct CDS Control icon ( ).

The Device Control dialog opens.

Figure 3-6 Device Control (CDS)

2. Click Start.

Stop the CDS

1. On the status panel, click the Direct CDS Control ( ) icon.

2. Click Stop.

Flush the CDS




Before installing a different calibrant solution, be sure to flush the CDS tubing to remove any existing calibrant.This procedure applies to both CDS bottles.

Required Materials

• Bottle of wash solution (1:1 water:acetonitrile)

• Waste container

1. Remove the calibrant bottle.

2. Put both ends of the calibrant tubing into a waste container, taking care not to submerge the tubing in liquid.

The container must hold at least 20 mL of additional solution that might come out of the instrument.

3. In the SCIEX OS, follow these steps to put the CDS into Wash mode:

a. On the status panel, click the Direct CDS Control icon.


Figure 3-7 Device Control (CDS)

b. Select Wash Mode.

This allows the pump to be controlled through the bottle sensor, which is located behind the bottle position.

4. Start the pump by pressing and holding the bottle sensor switch for 1 minute.

The CDS draws in air and discharges liquid. To stop the pump, stop pressing the switch.

5. Discard the waste.

6. Put the intake (left) tube into the bottle of wash solution.

7. Put the return (right) tube into the waste bottle.



8. Make sure that the software is still in Wash mode.

9. Press the bottle sensor switch for 1 minute or until 20 mL of solvent accumulates into the waste container.

10. Discard the waste.

11. Repeat step 2 to step 5 to purge the wash solution.

12. (Optional) Repeat step 6 to step 9 to flush the CDS with the new calibrant, putting the intake tube into thenew bottle of calibrant solution. To conserve sample, purge for only 10 seconds, or until 2 mL to 3 mL of solutionaccumulates in the waste container.

Tip! We recommend that the tubing be flushed with the new calibrant solution before the new calibrant isallowed to recirculate back into the calibrant bottle.

13. In the SCIEX OS, clear Wash Mode.

14. Put the return tubing into the calibrant bottle, and then install the bottle.



Use the Configuration workspace to:

• Activate and deactivate devices

• Add and delete devices

• Edit device settings

• Test the devices

Add Devices

1. Open the Configuration workspace.

2. Click Devices in the left panel.

3. Click Deactivate.

4. Click Add.

The Device dialog opens.

5. In the Type list, select the required type.

6. In the Model list, select the required model.

7. Click Settings to edit settings or restore default values.

8. Click Test Device to verify that the device is configured correctly and available for use.

9. Click Save.

10. Repeat step 4 to step 9 as required.

11. Click Activate Devices.

All of the devices that are selected in the Devices list are activated.

Edit Device Settings





4Configure Devices

4. Select either the integrated system or the mass spectrometer.

The Included check box is selected.

5. Click Edit.

The Device dialog opens.

6. Edit the devices as required.

• Click Settings to view information about the device components, restore device default values, and testthe device.

• Click Test Device to verify that the device is configured correctly and available for use.

7. Click Test Device.

If the test is successful, then a green informational message is shown. Otherwise, an informational messageindicates that the configuration is not valid and requires updates.

8. Click Save.



Delete Devices

Note: If the device that is being deleted is part of an integrated system, then all of the devices in the integratedsystem are deleted. Users cannot delete one device in an integrated system.

1. Open the Configuration workspace



4. Select a device.

5. Click Delete.



Deactivate Devices




Configure Devices



Configure Devices

Only a user who has been assigned to the Administrator or Method Developer role can perform this task.

Users OverviewIf a user has access to this feature, then the tile is labeled Users. If a user does not have access, then the tile ishidden.

Roles and PermissionsUsers can be assigned to more than one role.

Table 5-1 Role and Permissions

ReviewerAnalystMethodDeveloper

AdministratorPermission

NoYesYesYesAccess the Queue workspace

NoYes*YesYesAccess the Batch workspace

NoNoNoYesAccess the following quantitationsettings:

• Project Secure Export Settings

• Enable Project Modified PeakWarning


5Configure Access to the Software

Table 5-1 Role and Permissions (continued)



NoNoYesYesAccess the following advancedquantitation settings and features:

• Project Integration Defaults

• Project Units & CalibrationDefaults

• Create processing methods

• Export Results Table’sQuantitation Method as*.qmethod

• Export and save unlocked ResultsTables

• Create reports and save unlockedResults Tables

• Modify column settings

• Add custom columns

• Unlock Results Tables

YesNoYesYesTransfer to LIS

NoYesYesYesAccess the following basicquantitation settings and features:

• Create Results Tables

YesYesYesYesReview results

NoNoYesYesLC methods

NoNoYesYesMS methods

YesYesYesYesExplore data

YesYesYesYesView logs

NoNoNoYesArchive logs

NoNoYesYesConfigure the LIS

NoYesYesYesConfigure devices


Configure Access to the Software

Table 5-1 Role and Permissions (continued)



NoNoYesYesConfigure the device advancedoptions

NoNoNoYesAccess the Users workspace to addusers and assign roles

NoNoYesYesOptimize the mass spectrometer

NoNoYesYesAdd projects

*Analysts can only acquire data with locked MS and LC methods

Access to Analytics Features

Note: The controlled ways to output data from the Analytics workspace are: exporting Results Tables, transferringdata to a LIMS, and reporting. The other sources of output data such as copying and pasting from Results Tablesare not controlled. Do not use uncontrolled output methods for regulated purposes.

Table 5-2 Access to Analytics Features



NoYesYesYesCreate session file

NoNoYesYesCreate processingmethods

NoNoYesYesModify processingmethods

NoNoYesYesExport and createreports of unlockedResults Table

YesNoYesYesReplace existingResults Table whensaved

NoNoYesYesChange defaultprocessing methodsettings



Table 5-2 Access to Analytics Features (continued)



NoNoYesYesChange the defaultprocessing methodintegration algorithm

NoNoYesYesModify defaultprocessing methodintegrationparameters

NoNoNoYesAllow Enable ProjectModified PeakWarning

NoNoNoYesAllow Project SecureExport Settings

NoYesYesYesAdd samples to theResults Table

NoYesYesYesRemove samplesfrom the ResultsTable

NoNoYesYesModify the SampleName

NoYesYesYesModify Sample Type

NoNoYesYesModify Sample ID

NoYesYesYesModify ActualConcentration

NoYesYesYesModify DilutionFactor

NoNoYesYesModify CommentFields

NoYesYesYesAllow manualintegration

NoYesYesYesAllow Set to PeakNot Found






NoYesYesYesInclude or exclude apeak from the ResultsTable

NoNoYesYesModify theconcentration unitsand regressionsettings for fit andweight

NoYesYesYesModify the ResultsTable integrationparameters for asingle chromatogram

NoYesYesYesModify theprocessing methodfor the Results Tablecomponent

YesYesYesYesCreate, use, or exportMetric Plots inResults Tables

NoNoYesYesAdd, Rename, orModify customcolumns

NoNoYesYesRemove customcolumns

NoNoYesYesModify Results Tablecolumn settings

NoNoYesYesSave Column Settingsas Project Default

YesYesYesYesLock and save aResults Table

NoNoYesYesUnlock and save aResults Table

YesNoYesYesReview and save aResults Table






NoNoYesYesModify the barcode

NoNoYesYesExport, import, orremove ExternalCalibration

NoNoYesYesChange ComparisonSample assignment

NoNoYesYesAdd the MSMSspectra to library

Add Users

1. Open the Users workspace.

2. Click Add.

The Select User or Group dialog opens.

3. Add the user as required and then click OK.

4. Click OK.

The new user is included in the list of users in the left panel of the workspace.

5. Click the new user in the left panel.

6. In the right panel of the workspace, select a role or roles for the user.

Tip! Users can be assigned more than one role.

7. Click Save.

Deactivate a User


2. Click the user or group in the left panel.

3. Clear the Active check box.

4. Click Save.



Remove a UserUse this procedure to remove a user from the software. If a user is removed from Microsoft Windows, then theuser must also be removed from the SCIEX OS .


2. Click the user or group in the Users list.

3. Click Remove User.

Enable Full Screen ModeSelect this feature to use the SCIEX OS software as the primary application. Users cannot close the software oraccess other software programs.


2. Click General in the left panel.

3. Under General, select Enable to enable Full Screen Mode.

4. Click Save.

Select Laboratory Information Management System(LIMS) SettingsUse this feature to connect to an LIS server. Users can import batch information from, as well as export results to,an LIS.


2. Click LIMS Communication in the left panel.

3. Type the server address in the LIMS Server field.

4. Select the Enabled check box.

5. Click Save.

Select Queue OptionsThe queue goes one-by-one through the submitted list of pending samples or manually submitted samples, runningeach sample with the selected acquisition method. After all of the samples have been acquired, the queue stopsand the system goes to the Ready state. After the time set in the Instrument Idle Time field has elapsed, the system



goes to the Standby state. In the Standby state, the LC pumps and column oven are turned off and some massspectrometer voltages are turned off. The autosampler temperature control stays on to prevent sample degradation.

Only a user who has been assigned to the Administrator or Method Developer role can modify the length of timethe queue runs after the last acquisition has finished, before it puts the instrument in the Standby state.


2. Click Queue in the left panel.

3. Type the number of minutes that the system will remain in Ready state before moving to Standby state in theInstrument idle time field.

4. Type a number in the Maximum number of acquired samples allowed field.

5. Select the If a sample is missing, proceed to the next sample check box. The queue proceeds tothe next sample if a sample is missing.

6. Select the If calibration fails, proceed to the next sample check box. The queue proceeds to the nextsample if the calibration is failing.

7. Select the Save calibration data (in the current project) check box.

8. Click Save.

Select Regional SettingsThis feature applies the region and language settings selected in Control Panel. Only a period “.” or comma “,”can be used as a decimal separator. Digit grouping is not supported.


2. Click General in the left panel.

3. In the General panel, under Regional Settings, click Apply.

The regional settings that were set in the Windows operating system are applied to the software after thecomputer is started again.

4. Click Save.

5. Start the computer again.

Manage the Compound Libraries

Import a LibraryView Package

1. Expand the Compounds list in the Manage pane.

2. Click All Compounds.



3. Click the Import icon.

4. Click LibraryView Package (*.lbp) on the Library Importer dialog.

5. Navigate to the appropriate file on the Open dialog.

6. Select the file and then click Open.

7. Do one of the following:

• Click All above the Compound column on the Library Importer dialog to import all of the compounds.

• Click inside the appropriate row on the Library Importer dialog to import individual compounds.

Tip! To help locate compounds, use the Search field. As the search criteria is typed, the visible columnsare searched and refreshed to show only the information that matches the criteria specified.

8. Do one of the following to add the compounds to a library:

• Select the appropriate library from the Add to Compound Library list.

• Type the name of the library in the Add to Compound Library list field.

9. Click Next.

Note: If the user cancels the import before all of the compounds have been copied to the database, thenany compounds that have already been imported remain in the database. The software does not revert thedatabase to the pre-import state.

10. Resolve any conflicts, if required.

11. Click Finish.

Import a Compound Database





• Click DiscoveryQuant Compound Database (*.mdb) on the Library Importer dialog.

• Click Analyst Compound Database (*.mdb) on the Library Importer dialog.












9. Click Next.



11. Click Finish.

Import a Cliquid Package




4. Click Cliquid Package (*.clq) on the Library Importer dialog.












9. Click Next.

10. Type the name of the mass spectrometer in the Instrument Name field, if required, on the Instrument Namedialog.

11. Click OK.



13. Click Finish.

Import an Excel File




4. Click Excel file (*.xls) on the Library Importer dialog.



7. Select the appropriate Excel worksheet to import on the Library Importer dialog.

8. If the worksheet contains column headers, select the check box beside Selected Excel Worksheet hasheaders.

9. Type the name of the mass spectrometer in the Instrument Name field, if required, on the Instrument Namedialog.

10. Select the appropriate heading for each column of information.

Tip! Compound:CompoundId and Compound:Name are mandatory selections. Select ---[notused]--- for information that is not required.

11. Click Next.










14. Click Next.



16. Click Finish.

Import a Library Database Snapshot

CAUTION: Potential Data Loss. The information in this package overwrites all of the existingdata in the LibraryViewTM software database. The Cancel option is not available after theimport begins. It is recommended that a backup of the current database is created beforeperforming this procedure.




4. Click Overwrite Database with Library Snapshot (*.lbp) on the Library Importer dialog.

5. Click Yes on the Warning dialog.



8. Click Finish.



Import a Library Package from a Third Party




4. Click Third Party Library Package (*.tplp) on the Library Importer dialog.










9. Click Next.



11. Click Finish.

Install a Licensed LibraryView Package

Note: The LibraryViewTM software must be installed.

A licensed library can be installed from a DVD or from a .zip application file downloaded from the SCIEX Web site.The application file can include compound names, compound transition information, and compound library spectra.

1. Log on to the computer as a Microsoft Windows user with administrator privileges.




• If the library is being installed from a DVD, then load the DVD in the DVD drive and continue with step 5.

• If the library is being installed from a downloaded file, then continue with step 3.

3. Download the required .zip file from the SCIEX Web site.

Tip! To prevent potential installation issues, save the file to a location other than the computer desktop.

4. After the download is complete, right-click the downloaded file and then click Extract All.

5. Browse to the extracted files or the DVD and double-click Library.exe.

Tip! If the User Account Control dialog opens, then click Yes.

Tip! If the LibraryView Setup (Not Responding) message dialog opens, then close the message dialog,right-click the Library.exe file, and select the Run as administrator option to start the installationagain.

6. Click Software Activation on the LibraryViewPackages Feature Unavailable dialog.

The LibraryViewPackages Activation dialog opens.

7. Type the license key, exactly as shown, in the appropriate field.

If a license key is not available, then contact sciex.com/request-support.

8. Click Generate Computer ID.

This creates a unique identifier for the workstation.

9. Click Copy ID to Clipboard.

10. Follow the instructions to obtain the license.

Note: Internet access is required to obtain the license. If the computer does not have Internet access, thenmake a copy of the generated computer ID. On a computer with Internet access, go to the licensing page ofthe SCIEX Web site and then follow the instructions to obtain a license.

After the required information is submitted, a license file is sent to all of the e-mail addresses provided.

11. Close the browser window.

12. When the e-mail containing the license file is received, copy the license file to the workstation desktop.

13. Click Install License File on the LibraryViewPackages Activation dialog.

14. Browse to and then select the license file on the Select the new license file to be installed dialog.




15. Click Open.

Both the Select the new license file to be installed and the LibraryViewPackage Activation dialogs close.





17. Click Next.



19. Click Finish.

Compound ConflictsWhen installing a library containing a group of compounds or installing individual compounds, the softwaresearches the database for compounds with the same name or formula as a compound in the package. If compoundsare found, then the software flags the corresponding compounds in the package and waits for user input tocontinue.

Users have the option to:

• Merge the compound information. New spectra, transitions, and retention times from the compound in thepackage are added to the compound information stored in the database.

• Overwrite the compound information. Compound information from the package replaces the compoundinformation stored in the database.

• Keep the compound information. Compound information in the database is retained and the compoundinformation from the package is discarded.

Conflict information is available to help the user make the correct choice.

View Compound Conflicts

1. Click Resolve on the Library Importer dialog beside the compound to view the details of the conflict.




• Click Keep Original to keep the existing compound information and discard the new information.

• Click Use New to replace the existing compound information with the new information.

3. Repeat steps 1 and 2 for each compound.

4. Click Finish after all of the conflicts are resolved.

Merge Compounds


• Click Merge on the Library Importer dialog to merge new spectra, transitions, and retention times fromindividual compounds in the import package with the corresponding compound stored in the database.

• Click Merge All on the Library Importer dialog to merge new spectra, transitions, and retention timesfrom all of the compounds in the import package with the corresponding compounds stored in the database.


Overwrite Compounds


• Click Overwrite All on the Library Importer dialog to overwrite all of the compound information storedin the database with the corresponding compound information from the import package.

• Click Resolve beside the appropriate compound on the Library Importer dialog and then click Use Newto overwrite the compound information stored in the database with the corresponding compound informationfrom the import package.


Keep Original Compounds


• Click Keep All Original on the Library Importer dialog to keep all of the compound information storedin the database and discard the compound information from the import package.

• Click Keep Original beside the appropriate compound on the Library Importer dialog to keep the individualcompound information stored in the database and discard the compound information from the importpackage.




Add a Compound

Note: Compounds can also be added to a library using the Edit Library option.



3. Click the Add icon.

Note: The compound name is mandatory. All of the other information is optional.

4. Type the appropriate information in the fields on the Details tab.

5. Click Save.

Add a Mass Spectrum to a Compound



3. Double-click the appropriate compound.






7. Click the MS Spectra tab.

8. Click the Edit Mode icon.

9. Click the Add Spectra icon.

10. Click Open *.wiff file on the Add Mass Spectrum from *.wiff file to Compound dialog.

11. Browse to and then select the appropriate .wiff or .wiff2 file on the Open dialog.

12. Click Open.




• For IDA data, expand the sample and then select the appropriate compound in the navigation pane on theleft.

• For EPS, MRM, and looped data, select the appropriate sample.

14. Do one of the following to add spectrum to the compound:

• For IDA data, click Add Spectrum in the Acquired Spectrum pane.

• For EPS, MRM, and looped data, double-click the TIC and then click Add Spectrum in the AcquiredSpectrum pane.

15. Repeat steps 7 through 11 for each spectrum to be added.

16. Click Save.

17. Click Save on the MS Spectra tab.



About the Home PageThe home page consists of workspace tiles, divided into functions, the status panel, the ribbon, and the launcher.Access to workspaces is determined by the role assigned to the user as well as the software license. Within eachworkspace, the user can manually start acquisition or view and explore data that is being acquired.

Figure 6-1 Home Page


6Operating Instructions—Software

DescriptionItem

A light blue vertical line at the left side of a dark blue tile indicates that the workspace isopen, work is in progress, and that the user has access to the functionality. The status ofthe open workspace is shown on the tile.

1

A dark blue tile indicates that the workspace is closed.2

A gray tile indicates that the workspace is not enabled.3

The close icon (X) is shown in the top right corner of the tile when the workspace is open.4

Access to the launcher. The launcher contains a list of all of the workspaces. Click tothe right of the icon to open the launcher.

5

The ribbon. Refer to About the Ribbon and Launcher on page 67. To navigate to anotherworkspace, click a workspace from the list. The currently open workspace remains active

and the workspace icon is shown in the ribbon. To close the active workspace, click .

To return to the home page, click .

6

Functions: Acquisition, Processing, and Management. Access is dependent on the roleassigned to the user or licensing.

7

Status of the system. Click the title bar to show or hide the status panel.8

The status panel. Refer to About the Status Panel on page 69.9

About the Ribbon and Launcher

Figure 6-2 Ribbon

DescriptionItem

To navigate to another workspace, select a workspace from the list. The currently openworkspace remains active and the workspace icon is shown in the ribbon. Refer to Figure6-3.

1

Shows the name of the active workspace.2

To return to the home page, click .3

To go to an active workspace, click the workspace icon.4

Shows the currently logged in user.5


Operating Instructions—Software

DescriptionItem

Shows the system status. Refer to About the Status Panel on page 69.6

To open the Help, click the ?.7

Figure 6-3 Launcher

DescriptionItem

To show the list of workspaces, click .1

Shows the name of the active workspace.2

Shows the status of the workspaces. A dark blue background indicates that the workspaceis closed. A light blue bar at the left indicates that the workspace is active. A light bluebackground indicates that the workspace is open.

3

To close the active workspace, click .4

To close the open workspace, click .5



About the Status PanelThe icon and the color of the status bar change to indicate the status of the system. Use the status panel to dothe following:

• Add or select a project.

• View the samples remaining in the queue and the estimated time remaining for the batch to be acquired.

• View the system status or status of the individual devices that have been activated in Devices list in theConfiguration workspace.

• Access direct device control.

• View device details.

• Put the mass spectrometer or LC in Standby state.

• Verify and calibrate the TOF MS and TOF MS/MS modes.

• Equilibrate the system.



Figure 6-4 SCIEX OS Status Panel



DescriptionItem

Shows the status of the system. Click the title bar to show or hide the status panel.

• Ready is indicated by green

• Offline is indicated by gray.

• Equilibrating, running, and loading are indicated by blue.

• Stopped and stopping are indicated by yellow.

• Fault is indicated by red.

1

Shows the current project. Click the arrow to select an existing project. Click the plus signto add a project. Refer to Add a Project on page 71.

2

Shows the status of the samples in the queue.3

Shows the status of the devices. Click the title of the device to open the Device Detailsdialog and view the details.

4

Click the Direct Device Control icon to access controls for the device. The optionalsyringe can be started or stop on the Device Control dialog.

5

Shows the status of the device. The icon is a view-only indicator of the status of the device.6

Click to access MS Tune procedures to verify and calibrate the TOF MS and TOF MS/MSmodes.

7

Click the appropriate button to equilibrate the system or go to Standby mode.8

Add a ProjectThe project stores acquisition methods, data, batches, processing methods, processing results, and so on. Werecommend the use of separate project folders for each project.

Do not create projects or copy or paste files outside of the SCIEX OS software.

1. Click the plus sign next to the Projects list on the status panel.

2. Type a name.

3. Click OK.



Select a Project

• Select a project from the Projects list on the status panel.

Control the Device StatusUse this procedure to obtain detailed feedback on the status of a device. For example, temperatures, pressures,and voltages. To monitor the device status, click the icon at the far right of the device title.

1. On the status panel, click the Direct Device Control icon at the right of the device title.


2. Start, stop, or update the device, as required.

3. Click OK.

Show the Status Panel

• Click the colored bar at the top of the minimized status panel.

Hide the Status Panel

• Click the colored bar at the top of the status panel.

The status panel minimizes to the right of the workspace.

Data Acquisition PanelUse the Data Acquisition panel to start and monitor real-time data acquisition. Users can also edit the acquisitionmethod parameters during real-time data acquisition as well as save data or open data in the Explorer workspace.

Tip! Click the top of the Data Acquisition panel up or down to resize the contents.

Figure 6-5 Data Acquisition Panel



DescriptionLabelItem

Shows the TIC and spectrum.MS tab1

Shows the TWC and spectrum.DAD tab (Available only ifa DAD device is activated)

2

Calibration: ON : Indicates that the system is calibrating the massspectrometer using the masses in the selected reference table.

Ramping: ON: Indicates that parameters are being ramped. Rampinga parameter consists of automatically cycling an experiment whileincreasing or decreasing the value of a parameter every cycle.

Calibration: ON orRamping: ON

3

Click to start manual acquisition.Start4

Click Start > Start with LC to open the Start with LC dialog.Start with LC4

Click to stop manual acquisition.Stop5

Click to save data.Save6

Click to explore data in real time.—7

User Workflows

Analysts

Table 6-1 Analyst Workflow

Software AccessTask

Refer to About the Home Page on page 66 and Aboutthe Status Panel on page 69.

View the main screen and status panel to check thesystem status.

Refer to Batch and Queue Workspaces on page 74.Create and submit a batch either using an Excelspreadsheet, LIMS, or manually. LC and MS methodsmust be locked by method developers before batchesare created and submitted by analysts.

Refer to Batch and Queue Workspaces on page 74.View and manage samples in the queue.

Refer to Analytics Workspace on page 147.Process and review data in Results Tables.

Refer to Explorer Workspace on page 104.Explore data.



Method Developers

Software AccessTask

Refer to:• Operating Instructions—Hardware on page 36 and Configure

Devices on page 45.

• Define the Project Default Settings on page 148.

• Select Columns for the Results Table on page 154.

Configure the system.

Refer to MS Tune on page 192.Tune the mass spectrometer.

Refer to Operating Instructions—Hardware on page 36.Configure the LC devices.

Refer to LC Method Workspace on page 104.Create LC methods.

Refer to MS Method Workspace on page 88.Create MS methods.

Refer to Create a Processing Method on page 148.Develop processing methods.

Administrators

Software AccessTask

Refer to Select Laboratory Information Management System (LIMS)Settings on page 54.

Configure the LIMS.

Refer to Configure Access to the Software on page 48.Add users to the software and assign roles.

Refer to Archive Logs on page 197.Archive logs.

Reviewers

Software AccessTask

Refer to Analytics Workspace on page 147.Review processed results.

Refer to Explorer Workspace on page 104.Explore data.

Refer to View Logs on page 197.Review logs.

Batch and Queue WorkspacesThe Batch workspace shows a collection of information about the samples to be analyzed. Batches tell the softwarethe order in which to analyze the samples.



The Queue workspace shows the queue, batch, and sample status, so that the user can manage samples andbatches in the queue. The user can also access data from a specific sample in the queue by double-clicking thesample to open it in the Data Explorer workspace.

By default, the samples are not shown in the queue. Sample information is collapsed under the batch name. Thebatch status, the batch name, the number of samples in the batch, and the time remaining to acquire the currentbatch are shown. The calibration sample included in the batch is shown as Cal in the queue in the Sample Namecolumn.

Manage the BatchIn the Batch workspace, use the following features, as required.

Table 6-2 Batch Workspace Features

... do thisTo do this...

Click Manage > Cut.Cut rows

Click Manage > Copy.Copy rows

Click Manage > Paste.Paste rows

Click Manage > Insert Row.Insert a row

Click Manage > Delete Row.Delete a row

Click Manage > Select Columns. Refer to Show or Hide Columns onpage 87.

Select columns

Click Manage > Add component concentration column. Referto Add a Component Component Concentration Column on page 87.

Note: This component column is editable for all samples.

Add a component concentration

Click Manage > Delete component concentration column. Referto Delete a Component Concentration Column on page 87.

Delete a component concentration

Click a column and then click Manage > Apply currentconcentrations across all columns.

Apply a component concentration toall rows in a column

Click Print from the workspace menu.Print the batch

To save the batch to the current project, click Save > Save or Save >Save As from the workspace menu.

Save the batch

To export the batch as a .txt or .csv file, click Save > Export from theworkspace menu.

Export the batch



Import a BatchReview the batch contents before submitting the samples. Only a period "." is supported as decimal separator inimported .csv or .xsl files.

Users can edit imported batches as required.

Tip! To access the cut, copy, paste, add rows, and remove rows features, click Manage.

1. Open the Batch workspace.

2. (Optional) Select the columns that will be shown in the Batch workspace.

3. Click Open > Import from file.

4. Click Browse.

5. Navigate to the required file.

6. Click Open.

7. (Optional) Select or clear the Append to current batch check box, as required.

Note: Any existing data in the grid is overwritten if the user does not select the Append to current batchoption.

8. Click Import.

9. (Optional) Click Save.

10. Click Save As.

The Save As Batch dialog opens.

11. Type a file name in the File Name field and then click Save.

12. To use the plate layout as a reference for selecting or confirming a sample location, click Plate Layout.

The plate layout automatically provides well and vial positions for unassigned samples.

13. (Optional) To include calibration samples in the batch, do the following:

a. To open the Batch-Automatic Calibration Editor dialog, click Auto-Calibrate.

b. Select the ion reference and calibrant delivery settings to be applied automatically, at the specified frequency.

c. Click OK.

d. Select the check box to the left of the Auto-Calibrate button.

14. Make sure that the column oven temperature is reached before submitting the batch.

15. Make sure that the system has been equilibrated with the same MS and LC method.



16. Click Submit.

If errors are shown at the top of the screen, then resolve them and click Submit again. Any errors in the batchmust be resolved prior to submitting the batch.

To start sample analysis, make sure that the queue is started. If the queue is not started, then navigate to theQueue workspace and click Start on the menu bar.

Acquisition begins after the samples have been submitted from the Batch workspace.

Import a Batch from the LIMSReview the batch contents before submitting the samples.

Refer to Select Laboratory Information Management System (LIMS) Settings on page 54.




3. Click Open > Import from LIMS.

The Import a Batch File dialog opens.

4. Do the following:

a. Type the file location or file name.

b. (Optional) Click the Append to the current batch check box.

c. Click Import.



6. (Optional) To include calibration samples in the batch, do the following:

a. To open the Batch-Automatic Calibration Editor dialog, click Auto-Calibrate.

b. Select the ion reference and calibrant delivery settings to be applied automatically, at the specified frequency.

c. Click OK.

d. Select the check box to the left of the Auto-Calibrate button.


8. Click Submit.






Create a Batch ManuallyReview the batch contents before submitting the samples.




Tip! To use an existing batch, click Open > Open.

3. Click New.

4. Select an MS Method from the MS Method list.

5. (Optional) Select an LC method from the LC Method list.



7. Type the batch information in the grid.

8. (Optional) Click Save.


10. Make sure that the system has been equilibrated with the same MS and LC method.

11. Click Submit.




Batch Import Set Up

For the selected autosampler, the rack code, rack position, plate code, plate position, and vial position are alldependent on each other and only certain values are valid.



Table 6-3 Batch Import Set Up

Field Value RequirementsDefinitionColumn Name

Less than 50 characters. The Sample Namecannot contain these invalid characters: \/ : * ? " < > |=

Name of the sample.Sample Name

Less than 50 characters. The Sample IDcannot contain these invalid characters: \/ : * ? " < > |=

A custom number or otheridentifier for the sample.

Sample ID

Less than 50 characters.Unique ID from a sample.Barcode ID

The MS method must exist in the currentproject. The field is not case sensitive.

Name of the method.MS Method

The LC method must exist in the currentproject. The field is not case sensitive.

Name of the method.LC Method

The processing method must exist in thecurrent project. The field is not casesensitive.

Name of the method.Processing Method

Must be one of the valid choices for theautosampler specified in the LC method.

Describes the rack type for theautosampler.

Rack Code

Numerical value.The position of the rack on thetray.

Rack Position

Must be one of the valid choices for theautosampler specified in the LC method.

Describes the position of awell-plate in the autosampler.

Note: This column isunavailable if the Rack Codedescribes vials.

Plate Code

Match one of the predefined autosamplerplate positions.

The position of the plate on therack.

Plate Position

Numerical value. The largest value mustnot be larger than the number of vials inthe rack.

The position of the vial in a rackor on a plate.

Vial Position

Make sure that the sample type matchesone of the predefined sample types.Anything that does not match isautomatically replaced with Unknown.

The types of samples.Sample Type



Table 6-3 Batch Import Set Up (continued)

Field Value RequirementsDefinitionColumn Name

For SCIEX-developed methods, the valuemust be 1.00.

Value greater than zero and with sixdecimal places. The default value is1.000000. Do not leave the field blank.

The dilution factor for individualsamples.

Dilution factor

Must be less than 252 characters. The totalnumber of characters includes the numberof characters in the data subfolder path.The data file cannot contain any of theseinvalid characters: \ / : * ? " < > |=

The file name to which theacquired data is saved.

Data File

Must be less than 50 characters. This fieldcannot contain any of these invalidcharacters: \ / : * ? " < > |=

TextComments

Must be a name that was previouslydefined either in the MS method, for MRMscans, or in the processing method, forother scans. The name is validated duringmethod creation.

MRM HR scans: The name of acompound defined in the MRMmethod.

Other scans: The name of acomponent defined in theprocessing method.

The batch can contain up to500 compound or componentname columns. The name isused as the column name in thebatch import file that the usercreates.

Compound Name for MRM HR(MRM HR scans)

Component Name (other scans)

Use the Plate Layout Feature to Create a BatchThe plate layout feature provides a graphical representation of the rack and plate structures that can be used topopulate the grid in the Batch workspace.


2. Select an LC method.

The LC system must be active for the Plate Layout feature to be available.

3. Click Plate Layout.



The Plate Layout window opens and, by default, shows a graphical representation of the rack code .Subsequently, the window displays the rack code that was used last or the rack code specified for a currentlyhighlighted sample.

4. To change the rack code, click the arrow in the Rack Code field and then select the appropriate rack codefrom the list.

The window updates to show a graphical representation of the selected rack code.

5. On the graphical representation, click a sample position.

The selected sample position is fully highlighted in the graphical representation. The Batch workspace isupdated, starting with the first row that does not have the sample position defined completely, that is, a rowthat does not include the Rack Code, Plate Code (if using wells), and Vial Position values. The grid shows thesample positions accordingly.

6. Continue to select sample positions as needed in the graphical representation to populate the grid in the Batchworkspace.

If sample positions are typed directly in the grid in the Batch workspace, then the graphical representation isupdated accordingly.

7. To specify a replicate injection for a selected sample position, press Ctrl and then click the sample position inthe graphical representation.

The graphical representation shows the replicate sample position with a colored outline and the grid in theBatch workspace shows the data accordingly. Refer to Figure 6-6.

Figure 6-6 Plate Layout—Replicate Injection

8. To see the sample index in the graphical representation, move the mouse over the sample position.

A tooltip shows the sample index.

9. To remove a position, click a selected sample position in the graphical representation.

The sample position in the graphical representation is no longer highlighted and the data is removed from thegrid in the Batch workspace.



10. To remove all of the data associated with a specified rack code, click Clear All.

If the selected rack code identifies a plate, then the menu under Clear All includes Clear Front and ClearBack.For the specified rack code, all of the selected sample positions in the graphical representation are cleared andall of the data is removed from the grid in the Batch workspace.

Note: If the graphical representation includes replicate positions, then a warning message queries forconfirmation.

11. When all of the positions are assigned, click Close in the Plate Layout window and then click Save in theBatch workspace.

Create an Ion Reference Table


2. Click Auto-Calibrate.

The Batch - Automatic Calibration Editor dialog opens.

3. Click Edit.

The Ion Reference Table Editor dialog opens.

4. Click New.

Tip! Use the Tab key to move between cells and press Enter to add a row.

5. In the Reference Ions for TOF MS Calibration grid, type a precursor mass.

The Compound Name field is optional.

6. Add rows as required.

7. In the Use column, select the ions to use.

8. Select the Use for MS/MS radio button for the precursor mass to be used for MS/MS.

9. Type values in the CE for MS/MS and DP for MS/MS fields for the precursor mass selected in step 7.

10. In the Reference Ions for MS/MS Calibration grid, add and then select at least two fragment masses.

The Fragment Name field is optional

11. Click OK.

12. Type a name in the Save Reference Table dialog and then click OK.



Note: If users select an LC Method as the calibrant delivery method, then the Retention Time and theRetention Time Tolerance must be specified in the Reference Ions table.

Calibrate the System Using the CDS



The Batch - Automatic Calibration Editor opens.

3. Select an ion reference table.

4. Type the number of samples to be acquired between calibrations.

5. Select CDS as the calibrant delivery method.

By default, CDS channel 1 is selected. Use channel 1 for positive solutions and use channel 2 for negativesolutions.

6. Click OK to close the dialog.

7. Make sure that the check box to the left of the Auto-Calibrate button is selected.

8. Create and submit a batch.

Calibrate the System Using an LC Method



The Batch - Automatic Calibration Editor opens.

3. Select an ion reference table.

4. Type the number of samples to be acquired between calibration.

5. Select an LC Method as the calibrant delivery method.

The autosampler rack, plate, and vial fields as well as the MS method field are shown on the right of the dialog.

6. Select an MS method and then select the appropriate rack, plate, and vial information.

7. Click OK to close the dialog.

8. Make sure that the check box to the left of the Auto-Calibrate button is selected.

9. Create and submit a batch.



Equilibrate the SystemEquilibrate the system at the start of the day, before a new method is run, or before submitting a batch. Equilibrationwarms up and prepares the mass spectrometer for the next sample or batch.

1. Click Equilibrate on the status panel.

The Equilibrate dialog opens.

2. Select an MS Method from the MS Method list.

3. Select an LC method from the LC Method list.

4. Type the equilibration time in the Time (min) field, in minutes.

5. Click OK.

In the status panel, the system status is Ready when the equilibration is complete.

Manage the QueueAcquisition begins after the samples have been submitted from the Batch workspace. Make sure that the systemis equilibrated prior to submitting a batch. Refer to Equilibrate the System on page 84.

Note: Run the sample again in the event of an abnormal termination during sample acquisition. If the abnormaltermination is caused by a power failure, then the temperature of the autosampler tray is not maintained andsample integrity might be compromised.

1. Open the Queue workspace.

Note: Do not manually change the valve position during sample acquisition.

2. Use the features in Table 6-4 to manage the samples and batches in the queue.

Note: Only single batches or samples that have not been acquired can be moved.

Table 6-4 Queue Workspace Features


Click .View all of the samples in the batch.

Click .Collapse all of the samples in thebatch.



Table 6-4 Queue Workspace Features (continued)


Click Start. Equilibrate the system before running any samples.Start acquisition.

a. Click the sample.

b. Click Manage > Reacquire samples.

Reacquire a selected sample.


b. Click Manage > Delete samples.

Delete the selected sample.


b. Click Manage > Delete samples below row selection.

Delete all of the samples below theselected sample.

Click Manage > Clear queue.Clear the queue of all of the acquiredbatches or samples.

a. Select the samples or batches as required.

b. Click Manage > Clear all selections. .

Clear the queue of all of the acquiredselected batches or samples.

a. Click the batch header.

b. Click Manage > Move row to top.

Move the selected batch or sample tothe top of the queue.


b. Click Manage > Move row up.

Move the selected sample up in thequeue.


b. Click Manage > Move row down.

Move the selected sample down in thequeue.

Click Manage > Collapse all rows.Collapse all of the samples andbatches.

Click Manage > Expand all rows.Show all of the samples and batches.

• Double-click the sample that is in the process of being acquired.

• Click the Explorer workspace icon.

View data that is in the process ofbeing acquired.

Double-click the sample that has been acquired.View data from a sample that hasbeen acquired.



Table 6-4 Queue Workspace Features (continued)


a. Click Manage > Select Columns.

b. Select the Barcode and Scanned barcode check boxes in theSelect Columns dialog. Refer to Show or Hide Columns on page87.

c. Click OK.

View the barcode vials that are beingscanned.

a. Click Manage > Select Columns.

b. Select or clear the column check boxes, as required, in the SelectColumns dialog. Refer to Show or Hide Columns on page 87.

c. Click OK.

Show or hide columns.

a. Click Stop.

b. Select how to stop the acquisition in the Stop dialog.

c. Click OK.

Stop the queue.

Click Print from the workspace menu.Print the queue.

Submit a Single Sample to the Queue

1. Select the row index number of the sample.

2. Make sure that the system is equilibrated prior to submitting the batch.

3. Click Submit.




Submit Multiple Samples to the Queue


• Click Ctrl + the sample row index number of each sample.



• Drag up or down the list of index numbers.

Note: Samples are submitted in the order that they are selected and not in the order that they are shownin the batch.

2. Make sure that the system is equilibrated prior to submitting the batch.

3. Click Submit.




Show or Hide Columns

1. In the Batch workspace, click Manage > Select Columns.

2. Select or clear the column check boxes, as required, in the Select Columns dialog.

3. Click OK.

Add a Component Component Concentration ColumnUse this procedure to add a component concentration column to the batch.

Note: Component concentration columns added with this procedure are editable for all samples. Componentconcentration columns are also added to a batch when a processing method that contains components is definedfor a sample. These component concentration columns are only editable for samples with processing methodsthat contain the component.

1. In the Batch workspace, click Manage > Add component concentration column.

2. Type the name of the Component.

3. Click OK.

Delete a Component Concentration ColumnUse this procedure to remove a component concentration column from the batch.

1. In the Batch workspace, click Manage > Delete component concentration column.

A list of components is shown. It contains all components added with the Add component concentrationcolumn command, or when a MRM method or processing method was added to the batch.



2. Select the component from the list.

3. Click OK.

Queue Icons

Table 6-5 Queue and Acquisition Status Icons

DescriptionNameIcon

The sample or entire batch was acquired successfully.Passed

The sample was acquired, but the user stopped or extended the acquisition.Warning

The sample or any sample within the batch did not acquire successfully.Failed

The calibration sample did not meet the acceptance criteria. Double-click the iconto view the status report.

Failed

The sample or batch is being acquired.In Progress

The sample or batch has not been acquired yet or is not in the process of beingacquired.

Waiting

There was a barcode reading error or a mismatch of the barcode scan and thesample.

Barcode Warning

Shows the samples in the batch.Expand arrow

Hides the samples in the batch.Collapse arrow

MS Method Workspace

Create an MS MethodRefer to the following as required:

• MS Method Experiments on page 90

• About MS Methods on page 91

• MS Method Parameters on page 93

• Calculate the Dynamic Collision Energy for MS Methods on page 103



• Help system

1. Open the MS Methods workspace.

2. Click New and then click a method.

3. (Optional) Click Advanced and then select the following as required:

• Apply experiment scheduling: Select to apply retention time window when the experiments will be executed.For the looped experiments, one of the starting run times must be 0 and one of the stopping run timesmust be equal to the method duration time.

• Show advanced parameters: Select to show the advanced parameters, for example, time bins to sum andchannels.

• Apply intact protein mode : Select to show the intact protein mode fields.

• Ramp: Select to ramp parameters. Ramping a parameter consists of automatically running an experimentwhile increasing or decreasing the value of a parameter. Only one parameter can be ramped at a time, andthe steps must be in the same direction (either increasing or decreasing within start or stop values). Thisdialog enables the user to set the criteria to ramp a parameter. Users can set the starting and endingvoltages, and the size of the steps in between. Ramping can be used to optimize parameter for ions. ForTOF MS methods, users can ramp DP parameter. For TOF MSMS, users can ramp either the DP or CEparameter. Ramping can be enabled by selecting Apply ramping to the compound parameter.

• Calibrate: Select to calibrate the spectrum and the instrument on-the-fly. This dialog enables the user toselect the appropriate ion reference table for calibration. This feature is usually used with the CalibrantDelivery System. To view calibration results, users can go to the Queue workspace and then double-clickthe acquisition status icon of the calibration run. Calibration takes 1.25 mins.

• Dynamic collision energy: Click to open the Dynamic Collision Energy dialog.

4. Type values in the fields, as required.

5. (Optional) Click Add Experiment.

Tip! Use the list next to the Experiment field to change or delete the experiment.


• Click Save > Lock Method to save and lock the MS Method.

• Click Save > Save.



• Click Save > Save as.

MS Method ExperimentsRefer to MS Method Parameters on page 93.

Use the MS Method workspace to create or edit MS methods. An MS method can contain one or more experiments.By default, a new TOF MS method contains one experiment.

The types of MS experiments available are as follows:

• Three basic method experiments: TOF MS, TOF MSMS, and Q1

• Three combined method experiments: IDA, SWATH, and MRMHR

In addition, a step-by-step procedure is available to guide the creation of an MRMHR experiment. After the procedureis completed, the parameters are used to populate the MRMHR method.

Table 6-6 Basic Method Experiment

DefinitionType

Mass analysis using the TOF region. The m/z values of the ions are retained based ontheir flight time in the TOF region.

TOF MS

The precursor ion is selected using the quadrupole mass filter. Then m/z value of thefragment ions are returned based on their flight time in the TOF MS regions. This experimentis used to determine the structure of the compounds.

TOF MSMS

A data acquisition using the quadrupole mass filter. The ion intensity is returned for massesin the scan range.

Q1



Table 6-7 Combined Method Experiments

DefinitionType

An IDA (Information Dependent Acquisition) experiment analyzes data as it is beingacquired and changes experiment conditions according to the results of the analysis.Analysis of the results determine the masses on which to perform dependent scans. Theuser has total control over the criteria that activates an IDA experiment and the parametersof the IDA experiment that are activated.

IDA

SWATH® acquisition enables the MS/MS analysis of all precursor ions across a wide mass

range on an LC timescale. The Q1 quadrupole is set to a wider selection window width(typically 10 Da to 50 Da) than that used for conventional product ion acquisitions. Bystepping through multiple, sequential selection windows, a wide mass range is coveredrapidly. The resulting mass spectra are a composite of the fragments of all of the precursorions that passed through the respective Q1 selection window. This technique allows fornon-targeted MS/MS analysis of all species in a sample.

SWATH

The MRMHR experiment helps acquire high quality MS/MS data from compounds withknown masses and retention times. This acquisition can also be used to extract fragmentmasses with narrow widths (0.02 Da) from TOF MSMS spectra. The narrow extractiongives much better selectivity.

MRM HR

A step by step procedure to guide the creation of an MRMHR method. After the proceduresteps are completed, the parameters are used to populate the MRMHR method type.

Guided MRM HR

About MS MethodsAn MS method is comprised of the following elements:

• Parameters that pertain to the entire method, including Source and Gas parameters.

• One or more experiments.

• Each method must contain at least one experiment

• Any method can contain more than one experiment. This is referred to as looped experiments.

• The TOF MS and TOF MSMS experiments can be looped within a method, up to a maximum of 10experiments. Q1 experiments cannot be looped.

• The IDA, SWATH, MRMHR experiments can be looped within a method, up to a maximum of 2 experiments.

Note: Only specific combinations of experiments can be used, for example, IDA + IDA, SWATH + MRMHR.

• Each experiment has specific advanced settings.

• Individual scans within each experiment



Table 6-8 MS Methods Workspace Features

… do thisTo do this…

Click Add Experiment and then click an experiment type.Create a method with more than oneexperiment, that is, a loopedexperiments.

Click the list next to Experiment and then click an experiment types.Switch the experiment within anexisting MS method.

Click the list next to Experiment and then click Add IDA criteria.Convert a TOF MSMS experiment toan IDA experiment

Click the list next to Experiment and then click Delete TOF MS (ofMRM HR).

Note: Only applied to the looped experiments.

In an MRMHR experiment, removethe TOF MS from the method.

Click the list next to Experiment and then click Delete experiment.Delete an experiment when thereare multiple experiments within amethod.

Expand or collapse the Method Overview panel on the left side of theworkspace.

To view the following methodstructures:• The number of experiments

within a method.

• The scheduling duration of eachexperiment within the method.

• The number of TOF MSMS scansfor multiple experiments.



MS Method Parameters

Table 6-9 MS Method Parameters

ExperimentDefinitionParameter

TOF MS, TOF MSMS, Q1, SWATH, MRMHR, IDA

User-defined duration of the MS method.Method duration


The time required to execute each cycle. Includesexperimental times and overhead (the switchingtime between mass ranges and betweenexperiments). Use the total scan time to estimatethe number of points across the LC peak to obtainbetter quantitation results.

Total scan time

TOF MS, TOF MSMS, IDA, MRM HR,SWATH

Click to add an experiment.Add Experiment


The software calculates how many cycles areperformed based on the value in the Methodduration field.

Estimated cycles

IDA, SWATHSoftware automatically calculates the collisionenergy based on the m/z values and the chargestates for optimal performance.

Dynamic CollisionEnergy

TOF MS, TOF MSMS, IDA, SWATH, MRMHR

Shown when the Apply intact protein mode featureis selected. Select this feature when analyzing intactproteins that are larger than 10 KDa.

Intact proteinmode


Select this feature when analyzing intact proteinsthat are larger than 70 KDa. For example,monoclonal antibodies.

Large proteins(>70 kDa)


Select to decrease the signal from singly-chargedbackground ions without significantly impactingthe signal from multiply-charged proteins. Thisfeature improves the signal-to-noise ratio foranalyses with multiple charges.

Decrease detectorvoltage

Source Parameters

TOF MS, TOF MSMS, Q1, IDA, SWATH,MRM HR

Specify the gas flow between the curtain plate andthe orifice plate. Curtain GasTM interface flowprevents the contamination of the ion optics.

Curtain gas



Table 6-9 MS Method Parameters (continued)



Specify the ion source gas 1 flow. This parametercontrols the nebulizer gas for the TurboIonSpray

®

probe and the auxiliary gas for the APCI probe.

Ion source gas 1


Specify the temperature of the heater gas in theion source or the probe.

Temperature


Specify the ion source gas 2 flow. This parametercontrols the auxiliary, or turbo, gas for theTurboIonSpray

® probe. It is used to help evaporate

the spray droplets. Ion source gas 2 works inconjunction with the temperature parameter.

Ion source gas 2

TOFMS, TOFMSMS, Q1, SWATH, MRMHR, IDA

The CAD parameter controls the pressure of thegas in the collision cell. The collision gas helps tofocus the ions as they pass through the collisioncell; the preset for the CAD parameter is in fixedmode. For MS/MS scan types, the CAD gas helpsto fragment the precursor ions. When the precursorions collide with the collision gas, they dissociateto form product ions.

Use the preset value and optimize for thecompound.

CAD gas

Experiment


Select the polarity appropriate to the charge of theion of interest.

Polarity


The nebulizer current parameter controls the currentapplied to the corona discharge needle in the APCIprobe. The discharge ionizes solvent molecules,which in turn ionize the sample molecules.

Nebulizer current

TOF MS, TOF MSMS, Q1, IDA, SWATH,MRM HR, IDA

The voltage applied to the needle that sprays thesample. The spray voltage parameter affects thestability of the spray and hence the signalsensitivity.

Spray voltage






Ion Transmission coefficient (ITC) parameterattenuates the ion beam to avoid saturation andto prevent premature wear to the MCP plates. InTOFMS mode, the ion attenuation is adjusteddynamically by the software and a correspondingcorrection factor applied to the data output. In MS/MS, there is usually no beam attenuation so thecalculation is not necessary.

ITC

TOF MSMS, IDA, SWATH, MRM HRThe candidate ion that is selected for the TOFMSMS experiment.

Precursor ion

TOF MS, TOF MSMS, Q1, SWATH, MRMHR

The declustering potential parameter controls thevoltage on the orifice. It is used to minimize thesolvent clusters that might remain on the sampleions after they enter the vacuum chamber, and, ifrequired, to fragment ions. The higher the voltage,the higher the energy imparted to the ions. If theDP parameter is too high, then unwantedfragmentation might occur.

Declusteringpotential


The DP spread parameter (DPS), in conjunction withthe declustering potential (DP), determines thedeclustering potential applied to the ions. Thedeclustering potential is ramped from low to highdeclustering potential. For example, in positivemode, the declustering potential is ramped fromDP – DPS to DP + DPS. By entering a DPS value,declustering potential spread is automaticallyactivated.

DP spread

TOF MS, TOF MSMS, SWATH, MRM HR,IDA

The collision energy is the difference between theentrance potential (Q0) and the voltage on thecollision cell quadrupole (Q2). In MS/MS scans, thecollision energy provides the energy for collisionactivated dissociation (CAD). The collision energyis compound-dependent; that is, the optimum valuevaries from compound-to-compound.

Collision energy





TOF MSMS, IDA, TOF MS, SWATH, MRMHR

The CES parameter, in conjunction with theCollision Energy (CE), determines the collisionenergy applied to the precursor ion in a ProductIon scan. The collision energy is ramped from lowto high collision energy. For example, in positivemode, the collision energy is ramped from CE – CESto CE + CES. By entering a CES value, collisionenergy spread is automatically activated.

CE spread


Type the start mass for the scan range.TOF start mass


Type the stop mass for the scan range.TOF stop mass


The time required for the instrument to acquire oneTOF spectrum. The user can adjust the accumulationtime to optimize the total scan time.

Accumulation time

Q1Type the start mass for the Q1 scan range.Start mass

Q1Type the stop mass for the Q1 scan range.Stop mass

Q1The time required to scan the Q1 mass range.Scan time

SWATHClick to open the Autofill SWATH Windows dialog.Refer to the Help for more information.

Auto Fill SWATHwindows

MRM HRClick to open the Import and Auto-fill MSMS ScanInformation dialog. Refer to the Help system formore information.

Import and auto-fill

TOF MS, TOF MSMS, MRM HR, IDA,SWATH

Type the start time of the experiment.Start run time

TOF MS, TOF MSMS, MRM HR, IDA,SWATH

Type the stop time of the experiment.Stop run time

MRM HRSelect to apply MRMHR to each MRM transition.The fragment ion shows a window that is +/- 10Da centered on the fragment mass.

Apply fragment ionmass

MRM HRSelect to apply MRMHR to the precursor ion and thespecified fragment mass range. Users can enter thestart and stop masses for the fragment mass range.

Apply TOF start/stop mass





MRM HRSelect to apply the Retention Time window toindividual MRM transitions so that each MRMexperiment can be executed at the specified time.Users can enter up to 1250 Scheduled MRMHR

transitions when working with complex samples.

Apply ScanSchedule

MRM HRApply to sort the precursor masses in ascendingorder in the MS Table prior to acquisition. In somecases, acquiring MRM transitions in ascending ordermight improve MRM sensitivity.

Sort by precursorion

TOF MSMS, SWATH, MRM HR,Scheduled MRM HRTOF MSMS, TOF MSMS (SWATH), MRMHR and Scheduled MRM HR

For TOF MS scans, extends the linear dynamic rangeof measured components to higher concentrations.If this feature is selected, the cycle time might vary.

Note: When this feature is selected,accumulation time for MSMS experiments cannotbe set to less than 25 ms.

Enhance dynamicrange

Advanced Experiment Settings

TOF MSMS, Q1, IDASelect a resolution to use to separate closely spacedcomponents. Q1 resolution is the resolving abilityof the quadrupole. When more sensitivity isrequired in an MSMS experiment, the resolutionsettings can be reduced to allow more ions to beanalyzed. The Q1 resolution setting can be set toLow or Open to increase the intensity of theresulting signal or to allow more than just the C12isotope in any isotope pattern to be shown. Settingthe resolution to Open provides more signalstrength and allows more isotopes to be shown.

Q1 resolution

Q1Type the size of the scan interval in Daltons.Step size


Select the number of data points to be summed.Range for small molecule or peptides: 4 to 6.Starting value for Intact protein analysis ( > 20 kDa): 40

Time bins to sum


Select the time-to-digital converter (TDC) channels.Each channel counts ions. If all four of the channelsare selected (the default setting), then all fourchannels are summed for the total ion count.

Channels 1 to 4



Table 6-10 IDA Criteria

DescriptionLabel

IDA criteria are filters that are applied to the survey experiment, that is, TOFMS experiments.Only the ions meet IDA criteria are triggered for MS/MS experiments. In each applicationworkflow, the appropriate IDA criteria are selected and shown on UI. Or, the user can selectall workflow to choose desire criteria.

IDA Criteria

Specify the number of TOF MSMS experiments that are performed per cycle. If there arefewer candidate ions than the maximum candidate ions entered, then the time spent onMS/MS is distributed among the candidate ions. That is, the total cycle time is held relativelyconstant throughout the acquisition. All of the returned TOF MSMS spectra are normalizedto cps. In the software, users can add up to 100 TOF MSMS experiments per cycle.

Maximumcandidate ions

Select to prioritize the ions that are increasing in intensity in the TOF MS spectra, and thentrigger for MS/MS acquisition before the intensity starts to decrease. This filter removes theconstant background ions from the candidate list and triggers ions that are minor but areincreasing in intensity. The ions could be triggered multiple times when the signal-to-noiseratio is high. The dynamic background subtract filter can be used with the other standardfilters in the IDA criteria section.

Dynamicbackgroundsubtraction

Specify the minimum intensity (ion counts per second ) of the candidate ions for the TOFMSMS experiment.

Intensity thresholdexceeds

Select an option for ignoring previous candidate ions:• For (sec):

After the candidate ion has been selected for TOF MSMS experiment, do not consider itfor MS/MS for the next X seconds. It is recommended that this value to be set to halfthe LC peak width to ensure the candidate ion can be triggered at the peak apex.

• After _ occurrences:

In combination with For X seconds: Allows the candidate ion to be selected for MS/MSfor Y times in the following cycles during X seconds before being excluded from thecandidate list.

Note: Dynamic exclusion routine uses MW (not the m/z ratio). Candidate ions withthe same MW (within the mass tolerance) but difference charge states will be consideredto be the same candidate. The charge state that is the most intense survives on thecandidate list if the number of repeats has not been met. If the candidate ion has beenselected for MSMS once, and do not want to be triggered any more, in For (Sec) field,type in the method duration time as second.

Exclude formercandidate ions



Table 6-10 IDA Criteria (continued)

DescriptionLabel

The software automatically calculates the collision energy based on the m/z value and thecharge state of the ions. Refer to Calculate the Dynamic Collision Energy for MS Methodson page 103.

Dynamic CE can be used in combination with CE spread. The Collision Energy Spread (CES)is applied around the calculated collision energy.

Dynamic CE forMS/MS

Select to specify the charge state range of candidate ions. This helps to eliminate thesingly-charged background ions or unknown charged ions. This filter is typically used inpeptide application. When the charge state criteria is selected, only monoisotopic ions areselected for MS/MS.

Charge State

Advanced Criteria

Dynamic Accumulation helps to acquire high quality MS/MS data by assigning a longeraccumulation time to less intense ions and a shorter accumulation time to more intenseions. This ability to adapt MSMS accumulation time based on the precursor intensity can beused to improve the quality MS/MS spectra. If selected, the accumulation time is adjusted,that is, the shortest accumulation time is assigned to a higher intensity candidate, a longeraccumulation time is assigned to candidate ion with lower intensities. The total cycle timeis held relatively constant throughout the acquisition.

Dynamicaccumulation

Select to specify the m/z range for the candidate ions. The candidate mass range is alwaysthe subset of the TOF MS mass range.

Candidate massrange

Select to specify the isotopic exclusion window. This window is a symmetrical windowaround the candidate ion that was selected for MS/MS. Type the half-width of the window,that is, a value of four indicates that any peak that falls within the window M-4 to M+4 isnot selected in the same cycle as M for MS/MS. When this feature is activated, the peakfinder considers any unknown peaks as monoisotopic and +1 charge state. This is optimizedfor small molecular application.

Exclude isotopeswithin +/- Da

Select to automatically increase the magnitude of the CE by 9 V. When this field is selected,the Dynamic CE for MS/MS check box is automatically selected and not available.

Adjust CE whenusing iTRAQ

®

reagent

Specify the mass tolerance window. This window is a symmetrical window around thecandidate ion that was selected for MS/MS. Type the half-width of the window. For example,a value of 50 mDa indicates that any peak that falls within the window M-50 mDa to M+50mDa is considered to be the same peak as M, where M is the m/z value of the ion. Userscan select either ppm or mDa. Mass Tolerance can apply to the molecular weight withdynamic exclusion, or the m/z value of the ion.

Mass tolerance +/-mDa

ppm




DescriptionLabel

Select the check box to use the IDA: Inclusion List criteria. Click the link to open the IDA:Inclusion List dialog and edit the criteria.

Candidate ions that are on the inclusion list and meet the inclusion list criteria arepreferentially selected for MS/MS.

• Compound name: The name of the candidate ions. The name can include any charactersand does not have to be unique. The compound name is recorded in the file information.This field can be left blank.

• m/z (Da): Type the m/z value for the ions on which MS/MS is preferentially performed.

• Retention time (min): Type the LC retention time for the ion of interest. If the ion isdetected at the specified retention time, it is preferentially selected for MS/MS. Typinga value of 0 indicates that the ion is preferentially considered throughout the acquisition.

• Retention time tolerance (+/-sec): This value is the +/- time window around the specifiedretention time. Tolerance helps to account for any drifts in the LC retention time. If theion on the inclusion list is detected in the window around the specified retention time,then it is preferentially selected for MS/MS.

• Intensity (cps): Specify the intensity threshold for the ion on the inclusion list. If thecandidate ion surpasses the threshold (in cps), then it is preferentially selected for MS/MS.

Inclusion List

Select the check box to use the IDA: Exclusion List criteria. Click the link to open the IDA:Exclusion List dialog and edit the criteria.

Candidate ions that are on the exclusion list are not selected for MS/MS at the retentiontime specified.

• Compound name: The name of the candidate ions. The name can include any charactersand does not have to be unique. The compound name is recorded in the file information.This field can be left blank.

• m/z (Da): Type the m/z value for the ions on which MS/MS is not performed.

• Retention time (min): Type the LC retention time for the ion of interest. If the ion isdetected at the specified retention time, then it is not selected for MS/MS. Typing a valueof 0 indicates that the ion is not considered throughout the acquisition.

• Retention time tolerance (+/-sec): This value is the +/- time window around the specifiedretention time. Tolerance helps to account for any drifts in the LC retention time. If theion on the exclusion list is detected in the window around the specified retention time,then it is preferentially excluded for MS/MS

Exclusion List




DescriptionLabel

Select the check box to use the Mass Defect Filter criteria. Click the link to open the IDA:Mass Defect Filter dialog and edit the criteria.

MS/MS is triggered on any ion that meets the specified mass defect criteria. The IDA algorithmconverts the ion to its molecular weight and then compares the molecular weight to themass defect criteria. The mass defect filter can be applied to filter all of the ions that falloutside of the expected molecular weight range, as well as those ions that are within theexpected molecular weight range but exceed the expected mass defect range

Mass defect ( mDa ) = ABS ( mono mass - nominal mass )

• Chemical formula: Type the molecular formula of the representative compound of interest.Multiple formulae can be entered to allow for real-time multiple mass defect filtering.

• MW ( Da ): The software generates the mono molecular weight of the chemical formula.

• MW tolerance (+/- Da ): When a formula is entered, the software automatically calculatesthe associated molecular weight (MW).The MW tolerance (+/-Da) is the window centeredaround the calculated MW. If a candidate ion has a mass defect that meets the massdefect ± the mass defect tolerance, and falls within the window around the MW, thenit is considered for MS/MS.

• Mass defect ( Da ): Type the molecular formula and MW tolerance. The software calculatesthe mass defect of the entered formula.

• Mass defect tolerance (mDa): Type the tolerance around the mass defect.

Use the mass defect filter with no other IDA criteria: Select the check box to use the massdefect filter exclusively. MS/MS is performed only on candidate ions that have a mass defectthat falls within the given criteria. If this check box is not selected, then the candidate ionsthat meet the mass defect criteria have a higher priority in the candidate list over other ionsthat meet the rest of the IDA criteria specified, with the exception of the inclusion list.Candidate ions satisfying the inclusion list will have the same priority as those satisfyingthe mass defect criteria.

Mass Defect Filter




DescriptionLabel

Select the check box to use the Isotopic Matching criteria. Click the link to open the IsotopicMatching dialog and edit the criteria.

When isotopic match is selected, users can manually type the isotope pattern or use theIsotopic Calculator to calculate and then populate the isotope pattern that is used to triggerMS/MS. When typing the pattern manually, the first entry must have a mass difference of0 Da and 100% abundance. Subsequent entries in the Abundance column can be greaterthan 100% if the monoisotopic ion is not the most abundant ion in the isotope pattern.Isotope to use for TOF MSMS: Select which peak in the isotope pattern on which to performMS/MS. For example, monoisotopic ion or most intense ion.

Isotopic Calculator: Automatically calculate the isotope pattern based on a user-specifiedformula or charge state, and H+ charge agent if necessary. Type a formula in the IsotopicCalculator and then click Calculate. Click OK to close the Isotopic Calculator dialog. TheMass Difference and Abundance columns are automatically populated.

Note: The software removes any rows with abundance less than 1%.

Tolerance (mass): The mass difference for the specified peak in the pattern must be within+/- the tolerance to be a match for the pattern.

Tolerance (Abundance): This is the abundance tolerance in %. The abundance for the specifiedpeak in the pattern must be within ± the abundance tolerance to be a match for the pattern.

Isotopic Matching




DescriptionLabel

Select the check box to use the Neutral Loss criteria. Click the link to open the Neutral Lossdialog and edit the criteria.

When neutral loss is selected, the software compares mass lists from two TOF MS experimentswith different CE values (Low/High CE values), the precursor masses that have massdifferences within the tolerance (mass) are trigged for MS/MS.

Note: Only the precursor ion in a low CE survey scan is trigged by MS/MS. If the neutralloss filter is selected, then the neutral loss ions are exclusively selected for IDA experiments.CE values for the TOF MS method are not available after the Neutral Loss feature is selected.

• Low CE (survey scan): Set the collision energy that applies to the first TOF MS experiment.

• High CE (second scan): Set the collision energy that applies to the second TOF MSexperiment.

Note: High CE is greater than the Low CE value for positive polarity. Low CE is greaterthan the High CE value for negative polarity.

• Tolerance (mass): Specify the tolerance applied to the mass difference. The default valueis 0.02 Da.

Neutral Loss

Calculate the Dynamic Collision Energy for MS Methods

1. Open the MS Method workspace.

2. Create or open an MS method that contains IDA criteria or SWATH® application criteria.

3. Click Advanced > Dyanamic collision energy.

4. Modify the information in the fields, as required.


• To use previously saved default values to calculate the dynamic CE, click Load Default Settings.

• To save the current values as the default values to be used to calculate the dynamic CE in new methods,click Save as Default Settings.

• To apply the current values to the current method to calculate the dynamic CE, click Apply.

• To close the dialog and abandon any changes, click Cancel.



LC Method Workspace

Create an LC MethodRefer to the documentation that comes with the LC devices.

1. Open the LC Method workspace.

2. Click New.

3. Click a device in the left panel and then edit the fields, as required.

4. Save the file.

Explorer Workspace

Verify the Presence of an Analyte

1. Open the Explorer workspace.

2. Click File > Open Multiple Samples.

Figure 6-7 File Menu—Options

3. In the Select Samples dialog, select the samples from the Available list and then click the arrow to move thefiles to the Selected list.

Tip! To select one sample, expand the file, click the sample, and then click the arrow.



4. Click OK.

5. Click Show > Extract Ion Chromatogram (XIC).

Figure 6-8 Show Menu—Options

The Specify XIC Ranges dialog opens.

6. Type the Center, Width, and Compound values in the Specify XIC Ranges dialog. Refer to ExtractIons on page 105.

7. Click OK.

8. Click Show > Data and Peaks Table.


9. Review the peak area, intensity, masses, and charge states of the compounds.

Extract IonsUsed to calculate one or more overlaid extracted ion chromatograms (XICs), which is the plot of the intensity sumover a given mass range as a function of retention time.








4. Click OK.

5. Click Show > Extract Ion Chromatogram (XIC).


The Specify XIC Ranges dialog opens.

6. Type the Center, Width, and Compound values or import the values.

Note: The default title of the XIC includes the compound names shown in the cells for a given row.



Tip! When the Center/Width mode is used, a chemical formula rather than a mass can be specified forthe Center value. When a neutral composition is used (H20, for example) a proton is automatically addedfor positive mode or subtracted for negative mode (in the example the m/z of H3O+ is used for positive mode).Specify an explicit charge state by ending the composition with '+n' or '-n' where n is the charge state (ifthe n is omitted, then it is assumed to be one). For example, when H2ONa+ is specified the m/z of H2ONa+

is used as-is.

7. Right-click in the Specify XIC Ranges dialog and then use the features shown.

Figure 6-12 Specify XIC Ranges Dialog Right-click Menu

8. Click OK.

If the active graph contains overlaid series from different samples, then the Process All Overlays? dialog opens.

9. If the Process All Overlays? dialog opens, then do one of the following:

• Select All Overlaid to generate overlaid XICs for all of the available samples.

• Select Active Only to generate XICs only from the currently active sample.

If the Only show this dialog again if the Shift key is down check box is selected, then the selectedaction is always used unless the user holds the Shift key to change the option.



Open a Total Ion ChromatogramA total ion chromatogram (TIC) is created by summing the intensity contributions of all of the ions from a seriesof mass scans. Use the TIC to view an entire data set in a single pane. The TIC consists of the summed intensitiesof all of the ions in a scan plotted against time in a chromatographic pane.






4. Click OK.

5. Click Show > Total Ion Chromatogram (TIC).






7. Right-click in the TIC and then use the features shown in Figure 6-14.



Figure 6-14 Total Ion Chromatogram Right-click Menu


Available when there is more than one overlaid trace. Removesthe currently active trace from the graph. To remove a trace thatis not currently active, activate it and then select the feature.

Remove Active Trace1

Available when there is more than one overlaid trace. Removesall of the traces except the currently active trace. If the trace tobe kept is not currently active, then activate it and select thefeature.

Remove All Traces ExceptActive

2

Adds text to a graph.

If required, click Font to adjust the font properties and then clickOK. The caption is added at the (x, y) position where the userright-clicked to open the menu.

After the caption has been added, the user can drag it to a newlocation. If the user drags it into the x or y axis, then this cancelsthe drag operation.

The character sequences '\d' and '\u' are treated in a special way.In the former case, the one character immediately following isdrawn as a subscript and in the latter case as a superscript. Inboth cases, the special characters are not visible. This isparticularly useful for chemical formulae. For example, 'H\d3O\u+'is shown as H3O+.

Add Caption3




Right-click above a caption. The user can also open this dialogby double-clicking a caption.

Edit Caption4

Right-click above a caption and then select this feature.Alternatively, drag the caption outside the graph to delete it.

Delete Caption5

Available if the graph contains at least one caption. Removes allof the captions at once.

Delete All Captions6

Pastes an image in the graph.Paste Image7

Deletes the selected image from the graph.Delete Image8

Open a Base Peak ChromatogramGenerates a plot of the intensity of the largest peak in each spectrum as a function of time.






4. Click OK.



5. Click Show > Base Peak Chromatogram (BPC).


The BPC Options dialog opens.

6. Use the features shown in Figure 6-17.

Figure 6-17 BPC Options Dialog

Note: If a chromatogram with a single selection spanning more than 1.0 minutes is active when the basepeak chromatogram is being generated, then the time range defaults to the time range for the selection.Otherwise, the last time range is used. The limited time range saves the user from manually typing the range.




Figure 6-18 Process All Overlays? Dialog

LabelItem

Do you want to 'Show BPCs' for all overlaid data sets or only the active one?• All Overlaid

• Active Only

1

Only show this dialog again if the shift key is down2

OK3

Cancel4





Show the Data and Peaks TableThe Data and Peaks Table contains two different tables. The Data table shows the raw (x, y) values comprising adata set and the Peaks table shows information about the peaks themselves. The table is generated when a graphis active.

Note: Only peaks that are above the current threshold in the graph, set using the blue arrow on the y-axis ofthe graph, are present. Refer to Work with Data in Graphs on page 122.

This feature is used to show a pane containing two tables for the currently active data: one table for the raw (x,y) values and one for the peak list.








4. Click OK.

5. Click Show > Data and Peaks Table.




Use the features in Table 6-11.

Table 6-11 Data and Peaks Features


Click the column heading.Sort the table based on that field.

Right-click in the table and then click Copy. If the Data tab is active,then the selected x and y values are copied. Otherwise, if the Peaks tabis active, then the selected peak information is copied.

Copy the currently selected cells.

First select the rows by dragging in the row-selector column using theShift or Ctrl keys to select multiple rows.

Copy only selected rows.

Hold the Ctrl key and then click the column headings. If the user justclicks a column heading, then the column is sorted.

Select multiple columns.

Click Edit > Select All and then click Edit > Copy.Copy the entire table.

Right-click in the pane and then click Export Data as Text.

Saves the entire data list to the specified file. The x and y values areseparated with a tab and there is a carriage return after each (x, y) pair.

Export data as text.

Right-click in the pane and then click Export Peak List as Text.

Saves the entire peak list to the specified file. This does not include peaksthat are below the current threshold set in the y-axis of the associatedgraph. The various peak metrics are separated with a tab and there is acarriage return after each peak.

Export peak list data as text

Show Sample InformationThe Sample Information pane shows a textual description of the experiment used to acquire the active data. Thisinformation includes sample-specific information such as the sample name and information about the dataacquisition (number and type of the experiments, and so on).

If two or more Sample Information panes, associated with different samples, are visible, then clicking an item inthe tree view for any one of the panes causes all of the other panes to scroll to the corresponding section. Thisassumes that sections with the same names exist in all of the panes. This feature is useful if the user wants tocompare two similar, but not identical, Sample Information panes.








4. Click OK.

5. Click Show > Sample Information.

Show the Graph Selection InformationThis window shows information about the selected region in a chromatogram or spectrum and is generated whenone of those panes is active.








4. Click OK.

5. Click Window > Graph Selection Window.

The Graph Selection Info dialog opens.



Figure 6-23 Graph Selection Info Dialog

6. Make one or more selections in the graph.

Figure 6-24 Graph Selection Info

7. Select an option from the list: Default Info, XY Info, Standard Deviations, or Signal/Noise.

8. Use the features in Table 6-12 as required.



Table 6-12 Graph Selection Information

DescriptionLabel

Default Info

If the graph contains more than one selection, then information is listed separately for each.

The left and right x-values of the selection.Selected Start andEnd

The data point indices corresponding to the selected x-value range.Selected Points

The smallest and largest y-values for data points contained within the selected region.Min and Max

The sum of the y-values for the data points within the selected region.Sum

The x-value for the largest peak in the selection. If the peak-finder associated with thegraph did not find a peak in this region, then this field is not visible. In the case wherethe peak finder is not able to find a peak in the selected region, an extra field called Xat Max Y is present. This field contains the x-value corresponding to the point withinthe selection that has the largest y-value.

Peak

The width of the peak at half of its height. If no peak was found in the selected region,then this field is not shown.

Peak Width at 50%

The width of the peak in data points at half of its height. If no peak was found in theselected region, then this field is not shown.

Points Across Peak at50%

The width of the peak at its base. If no peak was found in the selected region, thenthis field is not shown.

Peak Width at Base

The width of the peak in data points at its base. If no peak was found in the selectedregion, then this field is not shown.

Points Across Peak atBase

The area for the largest peak in the selection. If no peak was found in the selectedregion, then this field is not shown.

Peak Area

XY Info

This view shows a subset of the information available in the Default Info view and is more convenient if theuser wants to copy the selected x-values (or y-values) so that they can be pasted elsewhere.

If a selection includes a peak detected by the peak finder, then this is the x-value foundby the peak finder (for the largest peak in the selection). Otherwise, this is the x-valuefor the data point with the largest intensity within the selection.

X-values

The maximum y-value in each of the selections.Y-values

The peak area of the largest peak in each of the selections.Peak Area

Standard Deviations



Table 6-12 Graph Selection Information (continued)

DescriptionLabel

When this option is selected, it is assumed that the selection spans a region that is of roughly constantintensity. Do not select this item if the selected region contains peaks.

The average of the y-values within the selected region and their standard deviation.Average and Std.Deviation

Signal/Noise

Make at least two selections in the graph, one containing a noise region and one containing a peak of interest.

The signal-to-noise (S/N) ratio of this peak is reported. The selection containing the largest y-value is assumedto contain the peak and the other selection the noise region. If the user selects more than two regions, thenthe one with the lowest y-value is assumed to be the noise region and the others to contain peaks of interest.

The average of the y-values and their standard deviation is shown for the noise region.Average and Std.Deviation

For the peak selection (or selections) this is the peak height minus the average y-valuefrom the noise region (that is, the peak height above the noise).

Subtracted Height

The calculated S/N ratio of the peak, which is the Subtracted Height of the peak dividedby the standard deviation of the noise region multiplied by a factor. This factor is theNoise Multiplier specified in the Options section. The noise multiplier is shown inbrackets in the output. The signal-to-noise as defined here is sometimes called theroot-mean-square (RMS) S/N because the standard deviation is the RMS of the presumednoise values with respect to their average.

Signal/Noise

The S/N calculated as the Subtracted Height of the peak divided by the entire range ofthe noise region (Max Y minus Min Y).

Peak-to-Peak S/N

9. (Optional) Click the Options icon.

The Graph Info Options dialog opens.

Figure 6-25 Graph Info Options Dialog




In the signal-to-noise ratio, the noise is defined as the standarddeviation of the points in the specified background regionmultiplied by this factor. Typically this factor is in the range 1 to3.

Noise multiplier for S/N1

Allows the user to change the percentage height at which theSum Y Above x% and Peak Width at x% fields arecalculated. Usually the default value of 50% is suitable and doesnot need to be changed.

Spectral height percentage2

Select to draw the information window as semi-transparent sothat any underlying data is still visible. When this feature is used,if the user activates the window by clicking inside it, then thewindow is drawn as solid. Use this feature if the graph isobscuring the information.

Semi-transparent (whennot active)

3

10. (Optional) Click the Fill Peaks icon.

In the active graph, switches between a mode in which peaks are filled using alternating dark and light fillsand a mode in which they are not. This feature is useful if the user wants to see the peak extent that correspondsto the Peak Width at Base.

11. (Optional) Click the Show Point Symbols icon.

In the active graph, switches between a mode in which data points are indicated with point symbols and amode in which they are not. This feature is useful if the user is closely examining a peak and wants to see howmany data points it comprises instead of using only the textual information shown in the main window.

Edit Settings in Graphs








4. Click OK.

5. Click Edit and then use the features in Figure 6-27.

Figure 6-27 Edit Menu—Options


Copies the current data to the clipboard. When a spectrum orchromatogram is active, a picture of this active graph is copied.

Copy1

When a spectrum or chromatogram is active, use this option tocopy the current graph to the clipboard as a picture.

Copy Graph2




Copies an image of the entire active window to the clipboard.The title bar of the window and the toolbars of its various panesare not included.

Copy Window3

Use this option to paste data from the clipboard into the currentview.

Paste4

When a table is active, selects all of the rows in the table. Whena text pane is active, selects all of the text.

Select All5

Allows the user to set options for the graph appearance, peaklabeling and finding, auto processing, and calculating the XICranges. Refer to Set Options on page 143.

Options6

Use this option to return to the default Explore options. Refer toReset Options on page 143.

Reset Options7

Work with Data in Graphs




3. Click OK.

4. To set the threshold for labeling peaks and subsequent features such as the Data and Peaks table, dragthe blue arrow that is shown on the y-axis of the graphs.



Figure 6-28 Blue Arrow on the Y-axis




Figure 6-29 Graph Menu—Options




Select portions of graphs to be processed in subsequentoperations. For example, select an area in a chromatogram andthen double-click to obtain an averaged spectrum. Use the SetSelection feature to type specific x-ranges so that selectionscan be set more accurately than is possible using the cursor.a. Click Graph > Set Selection.

b. In the Set Selection dialog, type the Center and Widthvalues.

c. Click OK.

Tip! To set selections in a graph manually, drag the cursor inthe plotting region to make a selection. If the Shift key is held,then any current selections are kept.

Set Selection1

Expands the y-values within a range by a specified factor forplotting purposes.a. Open a data file.

b. Select a portion of the graph.

c. Click Graph > Expand Selected Y-Values by.

d. In the Expand Selection dialog, type the expansion factor.

e. Click OK.

Expand Selected Y-ValuesBy

2

Removes all of the expansion ranges.• In a graph that has expanded ranges, click Graph > Clear

Expansion Ranges.

Clear Expansion Ranges3

This feature is available when there is more than one overlaidtrace. It removes the currently active trace from the graph.• In a graph that has more than one overlaid trace, click Graph

> Remove Active Trace.

Remove Active Trace4

This feature is available when there is more than one overlaidtrace. It removes all of the traces except the currently active one.• In a graph that has more than one overlaid trace, click Graph

> Remove All Traces Except Active.

Remove All Traces ExceptActive

5




Removes overlaid traces from the graph for which all of the datapoints are below the current threshold setting.

If the user zoomed the graph so that only a portion of the x-rangeis currently visible, then a dialog opens. The user can selectwhether to remove traces that are below the threshold using theentire range or using only the currently visible portion.

• In a graph that has more than one overlaid trace, click Graph> Remove Traces Below Threshold.

Remove Traces BelowThreshold

6

When the active graph contains more than one overlaid trace,draws all of the traces except for the currently active one usinga fainter, less intense, color than normal. Use this feature to focuson the active trace. The inactive traces are less distracting. Toreturn to the original style, select the feature again.• In a graph that has more than one overlaid trace, click Graph

> Fade Inactive Trace.

Fade Inactive Traces7

When the active graph contains more than one overlaid trace,using this option causes the second trace to be inverted. This canmake it easier to visually compare two similar traces. Select InvertSecond Overlay again to return to the original view.

Invert Second Overlay8

Replaces the graphs with a single trace that is the sum of all ofthe individual traces.• In an active graph containing more than one overlaid trace,

click Graph > Sum Graph Traces.

Sum Graph Traces9




Creates a graph for each separate overlay. For example, if theuser begins with a graph containing three overlaid traces andthen selects this feature, the final result contains four panes: theoriginal graph with the overlays and one graph for each of theindividual data sets.a. In an active graph containing more than one overlaid trace,

click Graph > Split Traces into Separate Panes.

b. In the Number of Columns dialog, select the number ofcolumns in the output.The number of rows required is determined based on thenumber of rows and the number of overlaid traces.

c. Select the check box to put the new panes into a new window.If the check box is not selected, then the new panes are placedin the same window.

Split Traces into SeparatePanes

10

Opens the Set Titles dialog. Use this option to manually changethe titles of the traces.

Set Graph Title(s)11

Opens the Color dialog. Use this option to set the color for thecurrently active graph trace.

Set Active Trace Color12

Opens the Set Trace Colors Using Pattern Matching dialog. Whenmultiple graph traces are overlaid, the software uses defaultcolors for the overlays. Use this option to set specific colors fortraces for which the title contains specific text.

Set Trace Colors UsingTitles

13

Creates a copy of the currently active graph data and then addsit to that graph. Use this feature to see the effect of a particulardata processing operation. For example, if the user duplicatesthe data using this feature and then smooths one of the twotraces, the resulting graph contains overlaid before and afterviews.• In an active graph, click Graph > Duplicate Active Data.

Duplicate Active Data14

Creates a copy of the currently active graph. Use this feature tosee the effect of a particular data processing operation. Forexample, if the user duplicates the data using this feature, andthen smooths one of the two traces, before and after views intwo separate graphs are visible. Link the x-axes so that zoomingone graph causes the other to zoom automatically.• In an active graph, click Graph > Duplicate Graph.

Duplicate Graph15




Opens the Offset Traces dialog. Use this option to create athree-dimensional stacked graph from a series of overlaid graphtraces.

Offset Traces in X and Y16

Use this option to remove the generated offsets from the TIC.Remove XY Offset17

Use the Two-Pane Operation Tools


2. Use the icons along the right edge of panes (refer to Table 6-13) to perform operations on two panes, thesource pane and the target pane. In all cases, click the icon in the source pane and then drag it to the targetpane.

Table 6-13 Two-Pane Tools

DescriptionNameIcon

Shown in the top right corner of each pane. It changes the relative positions of thepanes. Click the icon in one pane and then drag it to the top, bottom, left, or rightportion of a second pane. Depending on where the cursor is released, the first panechanges positions relative to the second. As the user drags the pane, one side of thesecond pane is highlighted in red to indicate where the first pane will be placed.

Note: The user can also drag panes from one window to another.

Move Pane

Used to sum two data sets together point-by-point. The data from the source panethat was originally clicked is added to the target pane (the pane over which the iconis released). The title of the modified pane updates to indicate that it has been modified.

Note: Only to add two data sets of the same type can be added. For example, theuser cannot add a spectrum to a chromatogram.

Tip! If the target graph contains more than one overlaid trace, then by default, thesource data is added to the active target data only. Hold the Ctrl key to add thesource to all data sets in the target pane.

Add Data



Table 6-13 Two-Pane Tools (continued)

DescriptionNameIcon

Similar to the Add Data icon except that the source data is subtracted from thetarget data. Use this feature to subtract background from a mass spectrum.

Tip! If the target graph contains more than one overlaid trace, then by default, thesource data is subtracted from the active target data only. Hold the Ctrl key to addthe source to all of the data sets in the target.

Tip! Normally any data points for which the intensity in the source is greater thanin the target are not kept. That is, negative y-values are discarded. Hold the Shiftkey to keep the points with negative intensity.

SubtractData

Overlays the active data in the source graph on the target graph. After the operationis completed the target graph contains a new series with a copy of the target data.

Tip! If the source graph contains more than one overlaid trace, then by default, onlya copy of its active data is moved to the target graph. Hold the Ctrl key to overlaya copy of all of the data sets in the source graph on the target graph.

OverlayData

Move Panes or Windows








4. Click OK.

5. Click Window and then use the features in Figure 6-31.

Figure 6-31 Window Menu—Options


Opens a window showing information for the selected region inthe active graph. For example, the x-range of the selection, theintensity range of the selected points, and so on). If this windowis already visible, then selecting the menu item closes it. Refer toShow the Graph Selection Information on page 115.

Graph Selection Window1

Use this option to change the layout of the information in thewindow from row format to column format.

Vertical Mode Pane Layout2




Removes the currently active pane from its window and placesit by itself in a new window.

Move Pane To NewWindow

3

Arranges any open windows (that have not been minimized) sothat they are all beside one another in one row.

Tile Vertically4

Arranges any open windows (that have not been minimized) sothat they are all above or below one another in one column.

Tile Horizontally5

Perform a Gaussian SmoothApplies a Gaussian smoothing algorithm. This is a filter of a specified width where the weighting factors followa Gaussian or 'normal' function.






4. Click OK.

5. Click Process > Gaussian Smooth.



The Gaussian Smooth dialog opens.

Figure 6-33 Gaussian Smooth Dialog

6. Type a value in the Smoothing width field.

This is actually the width of the Gaussian function at half of its maximum height. The total width is largerbecause the calculation is carried out into the wings of the Gaussian. Fractional values are allowed in whichcase the half width of the Gaussian is less than one point.

7. If there are multiple traces in the active graph, then select Process all overlays (otherwise active dataonly) to apply the operation to all of the traces.

If the Only show this dialog again if the shift key is down check box is selected, then the selectedaction is used unless the user holds the Shift key to change the option.

8. Click OK.

Threshold DataRemoves any data points that have an intensity below the current threshold setting. Sets the threshold by draggingthe blue arrow that is shown in the y-axis of graphs.








4. Click OK.

5. Click Process > Threshold Data.









Subset Data (to Graph Selection)This feature is only available when a graph with exactly one selected region is active. Removes data points lyingoutside the selected region. Use this feature to focus data processing on a subset of the entire data.






4. Click OK.

5. Make a selection in the graph.

6. Click Process > Subset Data (to graph selection).









Baseline Subtract ChromatogramRemoves a relatively slowly varying background from a chromatogram.

For each data point in the chromatogram, a window is centered at the corresponding x-value and the points withminimum intensity within the window to the left and right are found. A straight line is joined between these twopoints and the y-value is calculated at the center of the window. This is the baseline that is removed from the dataat that point.








4. Click OK.

5. Click Process > Baseline Subtract.

The Baseline Subtract dialog opens.

Figure 6-39 Baseline Subtract Dialog

6. Type a value in minutes in the Subtraction half window.





Offset ChromatogramUsed to offset the time values of a chromatogram.






4. Click OK.

5. Click Process > Offset Chromatogram.

The Offset dialog opens.



Figure 6-41 Offset Dialog

6. Type a value in minutes in the Total offset field.



8. Select the User incremental offset (to fan out overlays) to spread the overlays apart in the timedirection.

Centroid a SpectrumCreates a centroid of a mass spectrum, that is, replaces a profile spectrum with (mass, intensity) points for thedetected peaks only.








4. Click OK.

5. Click Process > Centroid Spectrum.

The Centroid dialog opens.


Figure 6-43 Centroid Dialog



Table 6-14 Centroid Dialog - Descriptions

DescriptionItem

For each peak, the centroid y-value is the intensity of the largest data point comprisingthe peak.

Intensity

This feature is similar to the Intensity feature except that the intensity is subtracted bythe baseline intensity in the case that there is a baseline offset.

Height

For each peak, the centroid y-value is the total area of the peak. This is a true integralin the sense that the reported value depends on both the intensity profile and the widthof the peak.

Area

For each peak, the y-value is the sum of the portion of the intensities comprising thepeak which are above 50% of the peak apex intensity. This value is useful because itdoes not depend only on the intensity of a single data point (as do the Intensity andHeight features) and it is not influenced by the edges of the peak which may be noisyor which may have interference.

Intensity sum above50%



Export Data as TextCurrently active spectrum or chromatogram is saved to a tab-delimited text file.








4. Click OK.

5. Click File > Export > Data as Text.

If spectral data is exported, then the Add Zero Intensity Points for Export dialog opens.

Figure 6-45 Add Zero Intensity Points for Export

6. Type a file name.

7. Click Save.



Export the Peak List as TextThe user can save the peak list for the currently active spectrum or chromatogram to a tab-delimited text file. Thisfile contains information such as the centroid x-value (mass or time), peak area, height, and so on.






4. Click OK.

5. Click File > Export > Peak List as Text.

6. Type a file name.

7. Click Save.

Print Data








4. Click OK.

5. Click File > Print and then select the required option.

Reset OptionsThe user can reset all of the options in the Explorer workspace to their default values. This includes the optionsdescribed in the previous section as well as processing options. Resetting the options only affects the currentlylogged-in Windows user, not other users of the same computer.


2. Click Edit > Reset Options.

Set OptionsUse the features on each tab as required.


2. Click Edit > Options.

The Options dialog opens showing the Graph Appearance tab.




Figure 6-48 Options Dialog—Graph Appearance Tab

4. Click the Peak Labeling & Finding tab.

5. Select Mass Spectra from the list.




Figure 6-49 Options Dialog—Peak Labeling & Finding Tab—Mass Spectra

7. Select Chromatograms from the list.


Figure 6-50 Options Dialog—Peak Labeling & Finding Tab—Chromatograms



9. Click the Auto Processing tab.

10. Use the features shown in Figure 6-51. Auto processing options do not apply to dynamically updating spectra.

Figure 6-51 Options Dialog—Auto Processing Tab

11. Click the XIC tab




Figure 6-52 Options Dialog—XIC Tab

13. Click OK.

Analytics WorkspaceAccess to features in this workspace are controlled by the role assigned to the user. Refer to Access to AnalyticsFeatures on page 50.

Note: The controlled ways to output data from the Analytics workspace are: exporting Results Tables, transferringdata to a LIMS, and reporting. The other sources of output data such as copying and pasting from Results Tablesare not controlled. Do not use uncontrolled output methods for regulated purposes.

The grouping of numbers is not supported in the Analytics workspace. Do not group numbers in any text box (forexample, integration parameters) or grid (for example, Results Tables).

Processing methods include the criteria used to quantitate the peaks selected for integration.

Reviewers should review the data according to the criteria of peak integration and data acceptance in their ownstandard operating procedures (SOPs).

Set Project Secure Export SettingsOnly a user who has been assigned to the Administrator role can perform this task.

If this option is selected, then data in the text file is encrypted during export. Set a password to enable encryption.



1. Open the Analytics workspace.

2. Click Projects > Project secure export settings.

3. Select the Encrypt Results Table when reporting for this project check box.

4. Type a password in the Password field.

5. Type the password again in the Confirm Password field.

6. Click OK.

Enable Project Modified Peak WarningBy default, this option is not selected. When selected, if a user makes a change to a chromatogram in a ResultsTable and then saves the changes, a warning message indicates that a change has been made. The user can chooseto continue saving or returning to the Results Table.

Define the Project Default SettingsThis option sets the default peak-finding parameters that are used when creating a processing method. If thereare more than a few components, then set the default values based on the chromatography so that they do notneed to be adjusted individually for every component. However, no one set of parameters is likely to be ideal forall components, so it might be necessary to adjust some of the parameters individually for some of the components.


2. Click Projects > Project default settings.

The Project Default Settings dialog opens.

3. Select an algorithm from the Integration Algorithm list on the Quantitative Processing tab.

Refer to the Help for information about the algorithms.

4. Select a library search algorithm from the Library Search Algorithm list on the Qualitative Processingtab.

Refer to the Help for information about the algorithms.

5. Click Save.

6. Click Close.

Create a Processing MethodProcessing methods contain quantitative and qualitative settings for data processing. The Non-targeted workflowis used for unknown components.


2. Click Process Method > New.



Tip! To edit an existing processing method, click Process Method > Edit embedded method andthen use the following steps.

3. Select the Workflow page and then select at least one workflow and the reference samples.

4. Select the Components page and then define the component names, masses, internal standards, groups, andso on.

Tip! If the group is defined in the Components table, then the user can choose to sum the ions in the group,even if the precursor ion and the experimental index are different for the transitions. The summed ions arenot shown in the table but are shown on the Integration page and in the Results Table as <group name>_Sum.This feature is useful for the quantitation of proteins and peptides.

Tip! Where the retention time of the components is not known, set the Retention Time Mode for amass or chemical formula to Find n peaks, where n is 1, 2, 5, 10, or all. The software identifies the specifiednumber of features with the greatest peak area, assigns the appropriate retention time, and then performsa targeted peak processing workflow. When processing is complete, the embedded method for the ResultsTable can be saved as a normal targeted method.

5. Select the Integration page and then select the integration parameters for each component.

6. Select the LibrarySearch (workflow-dependent) page and then define the library search parameters.

7. Select the Acceptance Criteria page and then select the acceptance criteria for peak integration, accuracy ofstandards and quality controls, and the calculated concentration range for the unknown samples.

8. Select the Qualitative Rules (Confidence Limit) page and then define the traffic light settings for mass accuracy,retention time difference, isotope match, library score, and formula finder score.

9. Select the Ion Ratio (Confidence Limit) page and then define the traffic light settings for the ion ratio acceptance.

Ion ratio is the peak response ratio (area or height of qualifier and quantifier).

10. Select the Formula Finder page and then select the formula finder settings.

11. Select the Non-targeted Peaks page (only available when the Non-targeted workflow is selected) and thendefine the Non-targeted search parameters.

12. Click Save.

Tip! When a Non-targeted method is created, the current project default parameters are used for peakintegration, and those parameters are saved in the method file. If the processing method contains the targetedanalytes, then the customized integration parameters for the targeted components will not affect theNon-targeted peak integration. If the user changes the project default parameter later, then the changedparameter will not impact the existing Non-targeted method, which still contains the parameters at the timethe method was created. Only the newly created non-targeted method use the changed parameters.



About Results TablesResults Tables summarize the calculated concentration of an analyte, as well as the qualitative analysis resultssuch as library hits, formula finder results, and so on, in each unknown sample based on the calibration curve.Results Tables also include the calibration curves, as well as statistics for the results. The user can customize theResults Tables and view the Results Tables in layouts.

The data from a Results Tables can be exported to a .txt file for use in other applications, such as Microsoft Excel.The user can export all of the data in the Results Table or just the data in the visible columns.

Tip! If multiple sessions of Results Tables have been tiled either vertically or horizontally, then click Views >Reset layout to return the Results Tables to their original layout.

Table 6-15 Right-click Menu

DescriptionLabel

Use this option to copy the current data to the clipboard.Copy

Use this option to paste data from the clipboard into the current view.Paste

Use this option to copy the entire table to the clipboard.Copy Entire Table

Use this option to replicate the information in the first selected row to allsubsequent selected rows.

Fill Down

Use this option to select all of the rows in the currently active Results Table.This is useful if the user subsequently wants to apply a command, such asCopy, that operates on the selected rows.

Select All Rows



Table 6-15 Right-click Menu (continued)

DescriptionLabel

If there is more than one analyte and all of the analytes are present in thesesamples at the same concentration, then use this option to provide a shortcutfor setting the actual concentration field for all of the analytes for the Standardsamples. To use this feature:1. Use the Components and Groups List to show only one specific

analyte in the table. Refer to Components and Groups List on page 168.

2. (Optional) Use the Sample Type filter to view only Standard samples.Refer to Sample Type Filter on page 153.

3. Specify the actual concentration for the analyte, either by typing directlyinto the cells or by selecting the column and pasting text into it.

4. Select Apply Current Analyte's Actual Concentrations to All.

Return to viewing all components and all sample types, as required.

Apply Current Analyte's ActualConcentrations to All

If there is more than one internal standard and all of the internal standards arepresent in these samples at the same concentration, then use this option toprovide a shortcut for setting the actual concentration field for all internalstandards for the Standard samples. To use this feature:1. Use the Components and Groups List to show only one specific

internal standard in the table. Refer to Components and Groups List onpage 168.

2. (Optional) Use the Sample Type filter to view only Standard samples.Refer to Sample Type Filter on page 153.

3. Specify the actual concentration for the internal standard, either by typingdirectly into the cells or by selecting the column and pasting text into it.

4. Select Apply Current IS's Actual Concentrations to All.

Return to viewing all components and all sample types, as required.

Apply Current IS's ActualConcentrations to All

Process Data


2. Click Results > New.

3. On the Process New Results page, use the arrows to select a sample batch.

4. Select a processing method from the list.



5. If required, click New to create a new processing method or click Edit to edit an existing processing method.Refer to Create a Processing Method on page 148.

6. Select a comparison sample for non-targeted workflows.

7. Click Process.

8. To show or hide sample types, click Sample Type and then select or clear the required check boxes.

9. To set the acceptance filters, click Acceptance and then select or clear the required check boxes.

10. To select qualitative confidence filters, click the Confidence traffic light and then select or clear the requiredcheck boxes.

Note: After the Results Table is generated using the AutoPeak algorithm, if the user changes the XIC widthand the expected RT, then the data will be reprocessed using the old algorithm model unless the user updatesthe model using the new XIC width and Expected RT values.

Refer to:

• Sample Type Filter on page 153

• About Results Tables on page 150

• Acceptance Criteria on page 153

• Confidence Traffic Lights on page 154

Add Samples

This option adds additional samples to a currently active Results Table.

1. With a Results Table open, click Results > Add samples.

2. In the Select Samples dialog, select the required samples.

• The Available pane shows the subfolders, .wiff2 files, and samples available in the Data folder for theselected folder.

• Expand individual folders to see any subfolders or .wiff2 files. If the .wiff2 file is expanded, it opens toshow the available samples.

• Use the arrows to add or remove samples.

• Select samples by double-clicking an individual sample, by selecting a sample or data file and then clickingthe => button, or by dragging a sample or data file from the left pane to the right one. Press Shift or Ctrlto select multiple files or samples before moving them.

3. Click OK.

A progress bar is shown while the new samples are integrated and added to the existing table.



Sample Type Filter

Table 6-16 Sample Type Filter Descriptions

DescriptionFilter Type

Shows only Unknown samples, which are normal samples of unknown concentration. WhenStandard samples are used, their concentration is back-calculated from the calibration curveand reported in the Results Table as the Calculated Concentration.

Unknowns

Shows only samples of known concentration. These samples are used for the creation of thecalibration curve.

Standards

Shows only Quality Control samples. These samples of known concentration are used tocheck the accuracy of the calibration curve but do not influence its actual construction.

Quality Controls

Shows only Blank samples. These are generally samples that contain the internal standardcompounds, if used, but no analytes, and that have been through the normal samplepreparation procedure. These samples are not used in the construction of the calibrationcurve. To include them, select the Standard sample type and then set the Actual Concentrationat 0.

Blanks

Shows only Double Blank samples. These are samples with neither internal standards noranalytes.

Double Blanks

Shows only Solvent samples. These are double blanks that have not been through the normalsample work-up procedure.

Solvents

Acceptance Criteria

Use the acceptance criteria to define a qualifying row. A qualifying row matches the selected criteria for thefollowing filters:

• Pass: Show the rows that match the criteria that was defined in the processing method.

• Fail: Shows the rows that do not match the criteria that was defined in the processing method.

• Any: Shows all of the rows.

Table 6-17 Acceptance Criteria

DescriptionLabel

Shows the user-defined criteria for integration quality using the value of the quality columnin the Results Table, asymmetry factor column, total width column, and the retention timeerror columns (either %error column or absolute delta column).

Integrationacceptance

Shows the accuracy of the standard and quality control samples tolerance.Accuracy



Table 6-17 Acceptance Criteria (continued)

DescriptionLabel

Shows the calculated concentration range for the unknown samples, obtained by editingthe lower limit or upper limit, or both.

Calculatedconcentration

Shows the rows that match the integration, accuracy, and calculated concentration filters(Pass/Fail/Any).

Show rows that:Qualify; Do notqualify

Confidence Traffic Lights

The traffic lights show the confidence status for each row. Refer to the Help for information on ion ratios andqualitative rules.

Table 6-18 Confidence Traffic Lights

DescriptionTraffic LightIcon

Shows which components meet the confidence levels defined in the processing method.

Shows which components meet the marginal percent difference level defined in the processingmethod.

Shows which components meet the unacceptable percent difference level defined in theprocessing method.

Shows which confidence parameters are not applicable for the component.

Select Columns for the Results Table

Select the numeric format and the columns to be shown in the Results Table. The column settings can be appliedto all of the Results Tables in the project.

Note: Some critical columns, such as Sample Name, Sample ID, Barcode, and so on, should not be hidden whenusers customize the Results Table column settings.

Tip! If column names are truncated, then move the cursor over the field to show the column name in a tool tip.

1. With a Results Table open, click More > Table display settings.

The Results Table Display Settings dialog opens.



Figure 6-53 Column Settings Dialog


Click to select a column settings file previously saved using theExport button. The dialog fields are updated to use theinformation from the selected file.

Import1

Click to save the current dialog settings to a file. Use the Importbutton to import and use these settings. This option lets the userswitch between different column layouts.

Export2

The name of the columns, shown in alphabetical order.Column Name3

A checkmark indicates that the column is visible.Visible4




For numerical fields, use the format 0.00 to for non-scientificnotations and use the format 0.00e0 for scientific notations.Change the decimal points to indicate the precision of thenumbers that are shown. Only a period "." can be used as adecimal separator.

Note: Grouping of numbers is not supported.

Number Format5

The selected LIS Supported rows are predefined by the LIS andthe column selections cannot be changed.

LIS Supported6

Click to use the column settings for future Results Tables.Save as project defaultsettings

7

Click to apply the changes and then close the dialog.OK8

Click to abandon the changes and then close the dialog.Cancel9

Select a category of Results Table columns. Users can filter thecolumns shown in the Results Table based on the selection.Selecting a category helps the user to easily find a column in theResults Table.

All Columns10

2. Select or clear the check box in the Visible column, as required.

Table 6-19 Results Table Columns

LIS SupportedDescriptionLabel

YShows the accuracy of standards and Quality Control samples.For other sample types, this value is set to N/A.

For standards of known concentration, the accuracy of standardsand Quality Control samples is defined as 100% × (CalculatedConcentration) / (Actual Concentration).

Accuracy

NShows the acceptance status of the accuracy.Accuracy Acceptance

YShows the name of the acquisition method used to acquire thesample.

Acq. Method Name

YShows the date and time at which the sample was acquired.Acquisition Date &Time

YFor standards and Quality Control samples, shows the expectedknown concentration.

ActualConcentration



Table 6-19 Results Table Columns (continued)


YShows the detected peak area. If no peak was detected, then thisvalue is set to N/A.

Area

NShows the detected peak area divided by the height. If a peakwas not detected, then this value is set to N/A.

Area / Height

YFor analytes using an internal standard, shows the ratio of theArea to the IS Area. For internal standards, or for analytes withoutan internal standard, this value is set to N/A.

Area Ratio

NThe area ratio of the sample/control sample. Applicable toqualitative workflows only.

• If no peak is found found in the control, then the value is N/A.

• If no peak is found in the sample, then the value is 0.

• If no peak in the sample is above the Area Ratio Threshold,then the value is N/A.

• If no comparison sample is used, then the value is "No controlsample".

• For the control sample, the area ratio for found peaks is always1.000.

Area Ratio ofControl

YShows the distance from the center line of the peak to the backslope, divided by the distance from the center line of the peak tothe front slope, with all of the measurements made at 10% ofthe maximum peak height.

Asymmetry Factor

YShow the unique ID for a sample. The unique ID is initialized fromthe value originally specified in the batch used to acquire thedata.

The barcode must contain between 0 and 20 characters and itcannot contain the following invalid characters: \ / : * ? " < > |=or characters 0 to 31 from the ASCII table.

Barcode

NShows the absolute value of the height difference of the baseline(at the start of the peak and the end of the peak) to the actualpeak height. Values greater than approximately 0.1 indicate thatthe baseline might not have been integrated correctly and thatthe peak should be reviewed.

Baseline Delta/Height





YFor standards of known concentration, shows the value of theback-calculated concentration from the calibration curve.Regression equations describe how the regression is performedfor the various regression types and weighting.

CalculatedConcentration

N(Optional) Shows a single number score that can be used forrelative comparison purposes. Applicable to qualitative workflowsonly.

Combined Score

NShows the components in the comparison sample. Users cannotedit this column.

Comparison

NShows an arbitrary comment for the analyte or internal standardthat applies to all of the samples.

ComponentComment

NShows the group name (if any) associated with the analyte orinternal standard.

Component GroupName

YShows the index of the analyte or internal standard in the originalprocessing method.

Component Index

YShows the name of the analyte or internal standard.

This column is always visible in the Results Table. In the ColumnSettings dialog, the check box is not available.

The component name must contain between 0 and 50 characters.

Note:

• The Component Name can only be changed in the processingmethod and not in the Results Table.

• This column is mandatory for a LIMS transfer.

Component Name

YShows the concentration units.Conc. Units

NShows the acceptance status of the calculated concentration.ConcentrationAcceptance

NFor analytes using an internal standard, shows the ratio of theActual Concentration to the IS Actual Concentration. For internalstandards, or for analytes without an internal standard, this valueis set to N/A.

Concentration Ratio

YShows the factor by which the sample has been diluted. Thisfactor is used in the calculation of the calibration curve.

Dilution Factor





YShows the ending retention time of the detected peak, in minutes.End Time

NShows the time, in minutes, along the back side of the peak wherethe intensity is at 10% of the peak height.

End Time at 10%

NShows the time, in minutes, along the back side of the peak wherethe intensity is at 5% of the peak height.

End Time at 5%

YShows the expected ion ratio for unknowns, Quality Controlsamples, and standards.

Expected Ion Ratio

YShows the original expected retention time from the processingmethod, in minutes.

Expected RT

Y(Optional) Shows a valid chemical formula. If the chemical formulais invalid, then it is not retained by the software. If the chemicalformula is valid, then the Mass (Da) and Isotope columns areauto-populated.

Formula

NShows the traffic light of the formula finder score. Applicable toqualitative workflows only.

Formula Confidence

NShows the single number score that can be used for relativecomparison purposes.

The value is can be updated using data from the Peak ReviewFormula Finder Results Table. Applicable to qualitative workflowsonly.

Formula Finder

N(Optional) Shows the best match of the formula finder results.Applicable to qualitative workflows only.

Formula FinderResults

Y(Optional) Shows a single number score that can be used forrelative comparison purposes.

Formula Finder Score

Y(Optional) Shows the best requested Fragment Mass (Da) at whichmatching spectra were found. Applicable to qualitative workflowsonly.

Found at Fragment

Y(Optional) Shows the best requested Extraction Mass (Da) atwhich the matching spectra were found. Applicable to qualitativeworkflows only.

Found at Mass

Y(Optional) Shows the fragment mass, as specified in the method.The precursor of the fragment is extracted from the MS/MS in theExtraction Mass (Da) column. When provided, this value must benumeric.

Fragment Mass





Y(Optional) Shows the difference between the Found at Fragmentand the Fragment Mass, in ppm.

Fragment Mass Error(ppm)

Y(Optional) Shows the difference between the Found at Fragmentand the Fragment Mass, in mDa.

Fragment Mass Error(mDa)

YShows the detected peak height. If peak was not detected, thenthis value is set to N/A.

Height

YFor analytes using an internal standard, shows the ratio of theHeight to the IS Height. For internal standards, or for analyteswithout an internal standard, this value is set to N/A.

Height Ratio

NShows the index of the row in the original, unsorted order. If thetable is sorted based on another column, then it can be returnedto the original order by sorting on this column.This column is always visible in the Results Table. In the ColumnSettings dialog, the check box is not available.

Index

YShows the volume of the sample stored in the method andinjected by the autosampler.

Injection Volume

NShows the integration outliers.IntegrationAcceptance

YShows the type of integration.

• Baseline: A standalone peak that was integrated in the usualway.

• Valley: Indicates that there were two adjacent peaks and thatthe signal did not return to the baseline value between them.

• N/A: Indicates that a peak was not detected.

• Manual: Indicates that the peak was manually integrated.

Integration Type





YShows the ion ratio.

• Ion Ratios are determined when at least two MRM transitionsfrom a single analyte have been collected into a group.

• The first component in a subgroup is used as Quantifier ions.The remainder of the components in the subgroup are usedas Qualifier ions.

• Ion Ratio = (Peak Area or Height of Qualifier) / (Peak Area orHeight of Quantifier)

• Subgroups

• All of the analytes in a group constitute an Analytesubgroup.

• All of the internal standards in a group constitute an ISsubgroup.

• If a component is not a member of a group, then the Ion Ratiovalue is set to N/A.

• If the peak is not found, then the Ion Ratio value is set to N/A.

• Applied to all of the components in both of the Analyte andIS subgroups, the Qualifier is itself for the Quantifier.

• If the integration changes for either of the Quantifier or theQualifier peaks, then the Ion Ratio is calculated again.

• Can be calculated for either the peak area or peak height. Ifthe Area is used in the regression part of a .qmethod for thefirst component (Component Index is 1) in the Results Table,then the peak area is used for the calculation of the Ion Ratiofor the entire Results Table. If the Height is used in theregression of the first component, then the peak height isused for the calculation.

Ion Ratio

NShows the level of confidence in the Ion Ratio. Applicable toqualitative workflows only.

Ion Ratio Confidence

NShows whether the row is an internal standard. A selected checkbox indicates that the component for the row is an internalstandard, not an analyte.

IS





NShows the actual concentration of the internal standard associatedwith the current analyte. For internal standards, or for analyteswithout an internal standard, the value is set to N/A.

IS ActualConcentration

NShows the area for the internal standard associated with thecurrent analyte. For internal standards, or for analytes withoutan internal standard, the value is set to N/A.

IS Area

NShows the ratio of the area to the height for the internal standardassociated with the current analyte. For internal standards, or foranalytes without an internal standard, the value is set to N/A.

IS Area / Height

NShows an arbitrary comment for the internal standard associatedwith the current analyte. For internal standards, or for analyteswithout an internal standard, the value is set to N/A.

IS Comment

NShows the time that the acquisition ends for the internal standardassociated with the current analyte. For internal standards, or foranalytes without an internal standard, the value is set to N/A.

IS End Time

NShows the expected retention time for the internal standardassociated with the current analyte. For internal standards, or foranalytes without an internal standard, the value is set to N/A.

IS Expected RT

NShows the height for the internal standard associated with thecurrent analyte. For internal standards, or for analytes withoutan internal standard, the value is set to N/A.

IS Height

NShows the type of integration for the internal standard associatedwith the current analyte. For internal standards, or for analyteswithout an internal standard, the value is set to N/A.

IS Integration Type

NShows the mass information for the internal standard associatedwith the current analyte. For internal standards, or for analyteswithout an internal standard, the value is set to N/A.

IS Mass Info

NShows the name of the internal standard associated with thecurrent analyte. For internal standards, or for analytes withoutan internal standard, the value is set to N/A.

IS Name

NShows the peak comment for the internal standard associatedwith the current analyte. For internal standards, or for analyteswithout an internal standard, the value is set to N/A.

IS Peak Comment





NShows the retention time for the internal standard associatedwith the current analyte. For internal standards, or for analyteswithout an internal standard, the value is set to N/A.

IS Retention Time

NShows the signal-to-noise ratio for the internal standardassociated with the current analyte. For internal standards, or foranalytes without an internal standard, the value is set to N/A.

IS Signal / Noise

NShows the start time for the internal standard associated withthe current analyte. For internal standards, or for analytes withoutan internal standard, the value is set to N/A.

IS Start Time

NShows the total width for the internal standard associated withthe current analyte. For internal standards, or for analytes withoutan internal standard, the value is set to N/A.

IS Total Width

NShows the width at 50% for the internal standard associated withthe current analyte. For internal standards, or for analytes withoutan internal standard, the value is set to N/A.

IS Width at 50%

NShows the level of confidence in the isotope ratio. Applicable toqualitative workflows only.

Isotope Confidence

NIdentifies the difference between the theoretical isotope pattern(based on the formula) and isotope pattern from the acquiredspectra.Applicable to qualitative workflows only.

Isotope RatioDifference

NShows the level of confidence in the Library Hit based on theLibrary score of the hit. Applicable to qualitative workflows only.

Library Confidence

NShows the compound name of the best library match, that is, thecompound with the highest purity score and the formula matchingthe requested formula.

The value is can be updated using data from the Peak ReviewLibrary Search Results grid. Applicable to qualitative workflowsonly.

Library Hit

NShows the difference between found mass and extraction mass,expressed in PPM (parts per million) error. Applicable toqualitative workflows only.

Mass Error (ppm)

NShows the level of confidence in mass error. Applicable toqualitative workflows only.

Mass ErrorConfidence





YShows the mass information associated with the component. ForMRM experiments this is Q1/Q3 and for profile (full scan)experiments it is Start - Stop.

For UV, ADC, or DAD experiments, it is the wavelength (DAD) orchannel information (UV/ADC).

If the fragment mass exists it will be used for XIC extraction.

If there is no fragment mass, then the precursor mass should beused for XIC extraction.

Mass Info

YShows whether the peak-finding parameters have been modified.A selected check box indicates that the peak-finding parametersindicated in the processing method have been modified, usingthe Peak Review pane.

Modified

NThe checkmark indicates whether the peak was found by theEnhanced Peak Finder. Applicable to qualitative workflows only.

Non-Targeted Peak

YShows the name of the instrument operator who acquired thesample.

Operator Name

YShows the name of the file.Original Filename

NShows an arbitrary comment for the row.Peak Comment

YShows the plate number of the autosampler used to acquire thedata, as indicated in the Batch Editor.

Plate Number

NShows the number of scans from the start to the stop of the peak.Points AcrossBaseline

NShows the number of scans across the peak, at approximately50% of the height.

Points Across HalfHeight

NThe processing input parameters taken from the processingmethod.

This column is always visible in the Results Table. In the ColumnSettings dialog, the check box is not available.

Precursor mass





NShows the purity score for the best library match.

The value is can be updated using data from the Peak ReviewLibrary Search Results grid. Applicable to qualitative workflowsonly.

The value can be updated from interactive data review. The valueis updatable from Peak Review Library Search Results grid.

Purity score

YShows the rack number of the autosampler used to acquire data,as specified in the Batch Editor.

Rack Number

YFor analytes that are using an internal standard, shows the ratioof the Retention Time to the IS Retention Time. For internalstandards, or for analytes without an internal standard, this valueis set to N/A.

Relative RT

YShows the actual retention time of the detected peak, in minutes.Retention Time

NShows the percent error found between "Found at RT" and"Expected RT". Applicable to qualitative workflows only.

Retention Time Error(%)

NShows the confidence in the retention time. Applicable toqualitative workflows only.

RT Confidence

YShows a user-specified comment for the sample.Sample Comment

YShows a user-specified identifier for the sample. The Sample IDis specified in the Batch Editor prior to sample submission foracquisition.

The Sample ID must contain between 0 and 50 characters and itcannot contain the following invalid characters: \ / : * ? " < > |=or characters 0 to 31 from the ASCII table.

Sample ID

YShows the index of the current sample.Sample Index

YShows a user-specified name for the sample. The Sample Nameis specified in the Batch Editor prior to sample submission foracquisition.

The Sample Name must contain between 1 and 50 charactersand it cannot contain the following invalid characters: \ / : * ? "< > |= or characters 0 to 31 from the ASCII table.

Sample Name

YShows the type of sample. Refer to Sample Type Filter on page153 for a description of the different filter types.

Sample Type





YShows the barcode scanned prior to the injection.Scanned Barcode

NShows the sample and component names that were used for peakmodeling. If the name of the component used for the modelingis not the same as the component that is integrated, then theuser should review if the model is appropriate.

SF Model Source

NShows the number of adjacent (convoluted) peaks detected bythe algorithm.

SF Num Peaks

YShows an estimate of the ratio of the peak height for the detectedpeak to the noise present in the chromatogram.

For the AutoPeak integration algorithm, noise is estimated usingthe calculated relative noise and the baseline at the peak apexposition. The MQ4 algorithm uses a similar approach, except thatthe baseline is estimated using the entire chromatogram.

Signal / Noise

YShows the starting retention time of the detected peak, inminutes.

Start Time

NShows the time, in minutes, along the front side of the peak wherethe intensity is at 10% of the peak height.

Start Time at 10%

NShows the time, in minutes, along the front side of the peak wherethe intensity is at 5% of the peak height.

Start Time at 5%

NShows the distance from the front slope of the peak to the backslope divided by twice the distance from the center line of thepeak to the front slope, with all of the measurements made at5% of the maximum peak height.

Tailing Factor

YShows the chromatographic peak width, in minutes, at thebaseline.

Total Width

YShows whether the analyte is sued for the construction of thecalibration curve. For standard samples, a selected check boxindicates that the corresponding analyte is currently used forconstruction of the calibration curve. For Quality Control samples,a selected check box indicates that the analyte is used for thecalculation of the quality control statistics. For other sample types,this field is for informational purposes only.

Used

YShows the vial number in the autosampler used to acquire data,as originally specified in the batch.

Vial Number





NShows the width of the peak, measured at 10% of the peakheight.

Width at 10%

NShows the width of the peak, measured at 5% of the peak height.Width at 5%

YShows the chromatographic peak width, in minutes, of thedetected peak measured at half of its apex intensity.

Width at 50%

3. (Optional) In the Number Format column, change the format to integer or scientific notation.

4. (Optional) In the Number Format column, change the number of decimal points to be shown.

5. To apply the column settings to all of the Results Tables in the project, select the Save as project defaultsettings check box.

6. Click OK.

The new settings are applied to the Results Table. The settings are also saved and applied when a new ResultsTable is created or a previously saved Results Table is opened again.

Note: Adjust the column widths and column order using the header row of the Results Table. Drag theheader border to change the width. Drag the column header to another location in the Results Table to changethe column order. The column width and the column order information is also saved to any exported fileswhen using the Export button.

Create a Report

1. With a Results Table open, click Reporting > Create Report and Save Results Table.

The Create Report dialog opens.

2. Select a template from the Template name list.

3. Select a report format.

4. Use the default report title or click Browse to select another.

5. Click the Create an individual report for each sample check box, if required.

6. (Optional) Click Replace Logo to select another logo for the report.

Tip! Use the options in the Replace Logo dialog to modify the logo as required.

7. Click View Pages to view the report.

8. Click Create.



Tip! If a user wants to report the selected results using, for example, one of the templates Per Sample Quant,Per Sample Qual, Per Sample Visible Rows Using Visible Analytes, or Positive Hits Qual, then the user shoulduse filters or hide the unwanted rows in the Results Table.

Note: User can view the report template layout by clicking the Template view in the Create Report dialog.To view a particular template, user must have a *.jpg file with same name as the template in addition to thesuffix [Snapshot_X](where X is the snapshot number in the sequence). Do not use spaces between the filename and the suffix.For example, All Peaks Qual.docx template would named: All Peaks Qual[Snapshot_1].jpg All PeaksQual[Snapshot_2].JPG All Peaks Qual[Snapshot_3].jpg

Export and Save a Results Table

1. With a Results Table open, click Reporting > Export results > Export and save Results Table.

The Export dialog opens.

2. Select the format, columns, and rows, as required.

3. Click OK.

Export Results Table – Metric

Note: The manufacturer assumes no responsibility or contingent liability, including indirect or consequentialdamages, after data has been exported from the Analytics workspace.

Exporting Results Tables is one of the controlled methods for data output in the Analytics workspace.

This feature is used to create a tab-delimited text file containing the information from the active Results Table.Information is exported for all samples and either all components or just the visible components for the one selectedmetric or field.

1. With a Results Table open, click Reporting > Export results > Results Table - Metric.

The Export dialog opens.

2. Select the format, columns, and rows as required.

3. Click OK.

Components and Groups List

When a Results Table is open, a list of the current components and groups is shown on the left side of the mainwindow. Use this list to change which components are visible in the results, as well as in any linked Peak Reviewor calibration curve windows . All of the information is shown as it was defined in the processing method.



Click an individual item in the list to show only the components for that item. Use Shift+click or Ctrl+click toselect multiple items, for example, two specific analytes.

Tip! Change the width of the list by dragging the right edge of the pane to the left or right.

The order of the rows in the Results Table is not affected by filtering. The table is preset to be ordered first bysample and then by component, in the order indicated in the processing method.

Table 6-20 Options

DescriptionLabel

Click to show the rows in the Results Table for both the currently selected analyte and thecorresponding internal standard. This is equivalent to clicking the analyte and then clickingthe internal standard while pressing Ctrl (so that both are selected).

Show IS

Click to find the items in the list that match the specified text.Find

Review PeaksUse the Peak Review pane to:

• Visually inspect the raw chromatograms so that the quality of the peak-finding process can be determined.

• Correct chromatograms that did not integrate properly ether by adjusting the peak-finding parameters or bymanually selecting the starting and ending points for integration. After a chromatogram is re-integrated, theResults Table is automatically updated with the new peak area and other parameters.

• Visually inspect the MS and MS/MS spectra for the integrated XIC.

• Review the Formula Finding results and Library Search results and, if necessary, manually update the resultsin the Results Table.

For information about the right-click features in the Peak Review pane, refer to Peak Review Options on page 171.For more information about Peak Review pane options, refer to Peak Review Options on page 171.


2. Click Results > Open.

The Open Results Table session dialog opens.

3. Select a file.

4. Click Open.

5. Click the Displays the peak review icon.

6. In the Components and Group list in the left pane, click a component.

7. (Optional) Click Options > Peak review display settings to change the appearance of the Peak Reviewpane.



8. If a chromatogram contains multiple peaks and an incorrect peak is integrated, then drag across the correctpeak to set a new expected retention time. If required, adjust the peak finding and integration parameters.

9. To apply the new parameters to all of the other samples, for the same component, right-click in thechromatogram and then click Update Quantitation Method for Component.

Tip! Integrated peaks can also be viewed by clicking the Starts ‘slide show’ peak review mode icon.Click the Displays the peak review icon and then click the Starts 'slide show' peak review icon.

Tip! Clear the integration by clicking Set Peak to ‘Not found’. The user can see the raw data beforemanually integrating the peak.

10. Click the Enable Manual Integration Mode icon in the Peak Review pane to use the manual integrationmode.

11. Drag the cursor from the base of one side of the peak of interest to the other.

The peak is now manually integrated and the integration parameters used previously are unavailable.

Tip! If the peak has just been modified, then revert the peak to the original method by right-clicking andthen clicking Revert Peak to Original Method.

View Options

In an open Peak Review pane, click View.

Table 6-21 View Options

DescriptionLabel

Click to view the chromatograms only.XIC

Click to view the chromatograms from different samples side-by-side. Users can selectup to six samples to compare the peak responses across the samples.

XIC side by side

Click to view the chromatogram and MS spectrum as well as the Formula Finder Resultsif they are available. If the formula is defined in the processing method, then thetheoretical MS spectrum can also be viewed.

XIC + MS

Click to view the chromatogram and MS/MS spectrum (if acquired), and the LibrarySearch Result if it is available. If there is a library hit, then the library MS/MS spectrumcan also be viewed.

XIC + MS/MS

Click to view the chromatogram, MS spectrum (and Formula Finder result), and MS/MSspectrum (and Library Search result). The theoretical MS spectrum and library MS/MSspectrum can also be viewed if they are available.

XIC + MS + MS/MS



Tip! The Formula Finder results are listed under the MS spectrum. The Library Search results are listed underthe MS/MS spectrum. Users can expand the pane to view more Formula Finder results and Library Search results.

Peak Review Options

In an open Peak Review pane, click Options.

Table 6-22 Peak Review Options

DescriptionLabel

Opens the Peak Review Options dialog. Use the options on the tabs to change theappearance of the Peak Review pane. Refer to the Help.

Peak review displaysettings

Switches the Y-axis scale from % to absolute.%Y-axis (spectraonly)

Fills the XIC and spectra with blue dots.Fill peak (XIC andspectra)

Shows the comparison of two selected MS spectra as a reflection of one another.Mirror MS spectra

Shows the comparison of two selected MS/MS spectra as a reflection of one another.Mirror MS/MSspectra

Shows or hides the integration parameters to the left of the Peak Review pane.Integrationparameters

Shows the navigation buttons. Click the buttons to move between components, movebetween samples, or start the slide show. Refer to Review Peaks on page 169.

Show navigationcontrols

Copy Integration Parameters

Right-click in the Peak Review pane to access this command. Use this command in conjunction with Paste IntegrationParameters to copy the peak-finding parameters from one chromatogram to another. This command can be usedif the same adjustment to the parameters needs to be made for several chromatograms.

1. In a graph with an active chromatogram open, right-click and then click Copy Integration Parameters.

2. Use the Update Processing Method for Component command to apply the change to allchromatograms for the component.

Paste Integration Parameters

1. In a graph with an active chromatogram open, right-click and then click Copy Integration Parameters.

2. Right-click in a different chromatogram and then click Paste Integration Parameters.



The previously copied parameters are applied to the new chromatogram.

Update Processing Method for Component

After adjusting the peak-finding parameters for a specific chromatogram, select this feature to modify the copyof the processing method saved with the Results Table to use those parameters for the component.

• Adjust the peak-finding parameters, right-click, and then select Update Processing Method forComponent.

For the particular component, all samples are automatically integrated to use the new parameters and thePeak Review pane and Results Table are updated. If any peaks have been manually integrated, then the useris asked if the re-integration should apply to all peaks or only to those that were not manually integrated.

Update Processing Method for Group

Similar to the Update Processing Method for Component command, except that the integration appliesto all components that belong to the same group as the component for the currently active chromatogram. If theuser has assigned the various components to groups, and if the components assigned to any given group areexpected to have the same retention time, then this feature is useful because it allows the user to reset theparameters, including the expected retention time, for all components for the group at once. This feature is notuseful if the components for the groups do not have the same retention times.

• Adjust the peak-finding parameters, right-click, and then select Update Processing Method for Group.

Apply Integration Parameters to Sample Within a Group

After adjusting the peak-finding parameters for a specific chromatogram, use this feature to apply the originalparameters from the copy of the processing method saved with the Results Table to the chromatogram.

• After adjusting the peak-finding parameters for a specific chromatogram, right-click and then click Applyintegration parameters to sample within a group.

Revert Peak to Original Method

After adjusting the peak-finding parameters for a specific chromatogram, use this feature to apply the originalparameters from the copy of the processing method saved with the Results Table to the chromatogram.

• In a graph with an active chromatogram open, right-click and then select Revert Peak to Original Method.

Revert All Peaks for Component

After adjusting the peak-finding parameters for some chromatograms, use this feature to apply the originalparameters from the copy of the processing method saved with the Results Table to all chromatograms for the



same component as the active chromatogram. If any peaks have been manually integrated, then the user is askedif the re-integration should apply to all peaks or only to those that were not manually integrated.

• In a graph with an active chromatogram open, right-click and then select Revert All Peaks for Component.

Analyze Peaks Using Library Search or Formula Finder Results

Tip! Click Options > Peak review display settings to change the number of rows shown in the pane.Users can also drag the top of the pane up to increase the size of the Peak Review pane.

1. In a Peak Review pane, click View and then click XIC + MS, XIC + MS/MS, or XIC + MS + MS/MS.

The search results are shown below the graphs.

Figure 6-54 Library Search Results

2. Click the blue arrow to expand the Library Search Results to show more possible library hits.

The chemical structure of selected library hit is also shown in the table.

3. Click the arrow again to collapse the table.

The results shown in the collapsed table are also shown in the Results Table.

4. (Optional) Select a row in the table and then click the icon in the table to update the results in the ResultsTable to use that specific library hit in the analysis.



5. (Optional) Click the icon to update the processing method with the information for the selected compound.

6. Click the blue arrow to expand the Formula Finder Results to show more possible results.

Figure 6-55 Formula Finder Results

The chemical structure of the selected formula finder results is also shown in the table if the compound hasbeen updated from ChemSpider.

7. Click the arrow again to collapse the table.

The results shown in the collapsed table are also shown in the Results Table.

8. Click to update the Formula Finder Results column in the Results Table with the selected compound.

9. Click to update the processing method with the information of the selected compound.

Tip! Click Options > Get Chemspider hit count to show the ChemSpider Hit Count column inthe table below the graph.

10. Click to open the ChemSpider application.

Refer to ChemSpider on page 175.



ChemSpider

Note: The workstation must contain a valid license file to access the ChemSpider database.

Note: Information in the following image is for example purposes only.

Figure 6-56 ChemSpider Session

DescriptionItem

Results pane: Shows a list of suggested compounds that match the selected formula. Theresults are shown in groups of 40 compounds. Use the right arrow to advanced to thenext group in the list. Use the left arrow to return to the previous group in the list.

1

Spectra pane: Shows the acquired spectra (in red) and the matching fragments (in blue).More blue fragments indicate a better match.

2

Structure pane: Shows the chemical structure of the compound selected in the resultspane.

3



DescriptionItem

Fragment table pane, Fragments tab: Shows the total number of matching fragments forthe selected compound.

4

Fragment table pane, Peaks tab: Shows the total number of peaks, the number of matchingpeaks, and the % of total intensity for the selected compound. The check box in theAssigned column is automatically selected for the matching peaks.

4

Table 6-23 ChemSpider Features

... this occursWhen you do this ...

The results pane is refreshed and contains only the results thatmatch the criteria entered.

Type information in the field beside the FilterXIC List icon.

The remaining panes refresh, showing the informationassociated with the selection.

Click through the entries in the results pane

The remaining panes refresh. In the spectra pane, red arrowsappear at the top and bottom of the matching fragment (inblue). In the structure pane, the components of the chemicalstructure that match the fragment are highlighted (bold).

Click through the entries on the Fragments tabof the fragment table pane

The remaining panes refresh. In the spectra pane, red arrowsappear at the top and bottom of the matching fragment (inblue). In the structure pane, the components of the chemicalstructure that match the fragment are highlighted (bold).

Click through the Assigned entries on thePeaks tab of the fragment table pane

The ChemSpider Web site (www.chemspider.com) opens in abrowser window. Refer to the ChemSpider Help for informationon accessing information.

Click the down arrow to the right of theChemSpider results for field and select theChemSpider web site option

All changes are discarded and the session reverts to theoriginal search results.

Click the down arrow to the right of theChemSpider results for field and select theRefresh option

The selected information in the ChemSpider session is copiedto the Formula Finder Results pane in the softwaresession. The ChemSpider session closes.

Click Select

About Statistics PaneTo access this dialog, open a Results Table in the Analytics workspace and then click Views > Statistics pane.



http://www.chemspider.com

Use the Statistics pane to view information related to the reproducibility of an analysis. Each row of the tablesummarizes information, such as the average and standard deviation for a group of related peaks, from the sameanalyte that would be expected to have the same response.

DescriptionLabel

The row number.Row

The name of the analyte.Component Name

When samples are grouped by actual concentration, this column shows theconcentration. When samples are grouped by sample name, this column shows thesample name.

Sample Name/ActualConcentration

Shows m of n where n is the total number of samples at the actual concentration (orwith the same sample name) and m is the number of these samples used for thecalculations. Samples are not used if the corresponding peak could not be integratedor if the Used field has been manually cleared.

Num. Values

The average of the used samples.Mean

The standard deviation of the used samples.Standard Deviation

The co-efficient of variance expressed as a percentage: 100 * (Standard Deviation) /Mean.

Percent CV

The mean value divided by the actual concentration expressed as a percentage: 100* Mean / (Actual Concentration). This field is shown only when grouping by actualconcentration, not when grouping by sample name.

Accuracy

The individual values for the samples are shown in additional columns. If thecorresponding sample could not be integrated, then N/A is shown. If the Used fieldhas been manually cleared, then the value is shown with a strikethrough.

Values



DescriptionLabel

The items in this list specify how the sample for a given analyte should be groupedfor the calculation of the statistics. The following choices are available:

• Group by Concentration for Standards: Standard samples are groupedby actual concentration.

• Group by Concentration for QCs: Quality Control samples are grouped byactual concentration.

• Group by Sample Name for Standards: Replicate Standard samples aregrouped by the Sample Name field.

• Group by Sample Name for QCs: Replicate Quality Control samples aregrouped by the Quality Control field.

• Group by Sample Name for All Samples: All replicate samples are groupedby the Sample Name field.

Group by Concentrationfor ...

The items in this list specify the actual metric that is used for the calculation of thestatistics. The following choices are available:

• Calculated Concentration: The Calculated Concentration field of the ResultsTable is used.

• Area: The Area field of the Results Table is used.

• Height: The Height field of the Results Table is used.

• Calibration Y-Value: The regression parameter specified for the analyte isused. This is either Area or Height for an analyte that does not have acorresponding internal standard, or Area Ratio or Height Ratio for an analyte thatuses an internal standard.

Calculated Concentration

Analyze Data Using Statistics

Use the statistics pane to view information related to the reproducibility of an analysis. Each row of the tablesummarizes information, such as the average and standard deviation, for a group of related peaks from the sameanalyte that would ideally be expected to have the same response.

Review the peak integration, the calibration curve, and the sample statistics using an iterative process. The precisionset for the Actual Concentration field in the Results Table is used in the statistics table as well.

Note: Refer to the laboratory standard operating procedures for information about accepted values for thestatistics, including %CV and Accuracy.

• Open a Results Table and then click Views > Statistics pane.



Refer to About Statistics Pane on page 176.

Calibration Curve: OptionsClick Options in an open calibration curve pane to use the following features:

Table 6-24 Calibration Curve Options

DescriptionLabel

When this option is selected, data points for excluded standards (if any) are drawn usingopen circles. When this option is cleared, excluded standards are not shown.

Show excludedstandards

When this option is selected, data points for Quality Control (QC) samples are drawn usingan open diamond. When this option is cleared, the QC samples are not shown.

Show quality controls

When this option is selected, a legend is drawn to the right of the plot that shows thepoint symbols for the various sample types (closed circles for standard samples, opencircles for excluded standards, and open diamonds for QC samples).

Note: If the user is not viewing specific sample types, for example, if the Show qualitycontrols option is not selected, then the entry for those sample types is not present.If neither QC samples nor excluded standard samples are shown, then this option is notavailable and no legend is drawn.

Show legend

When this option is selected, the Y-axis is expressed as a percentage of the data pointwith the largest y-value for each analyte, independently. When this option is cleared, theY-axis for the plot is expressed in units of absolute peak area or height (or the peak areaor height ratio if an internal standard is being used).

Using a percentage axis is useful if more than one analyte is overlaid and their absoluteresponses are different, because it allows each trace to be scaled to use the entire availablevertical area. Otherwise, analytes with a low response lie close to the X-axis and the plotmust be zoomed to see them in detail.

Use percent Y-axis

When this option is selected, the view between plotting Area versus Concentration andLog(Area) versus Log(Concentration) is toggled.

Log-log plot

When this option is selected, a previously exported calibration is applied to the activeResults Table.

Assign externalcalibration



Table 6-24 Calibration Curve Options (continued)

DescriptionLabel

When this option is selected, a previously applied external calibration is removed from anactive Results Table.

Remove externalcalibration

When this option is selected, a copy of the calibration equation for all analytes associatedwith the active Results Table is saved to an external file (*.mqcal). This allows thecalibration from one set of standard samples to be applied to other samples that are notpart of the same Results Table.

Export calibration(and save results)

Export Calibration

Use Export Calibration to save a copy of the calibration equation for all analytes associated with the active ResultsTable to an external file (*.mqcal). This allows the user to apply the calibration from one set of standard samplesto other samples that are not part of the same Results Table.

The typical workflow is:

1. Create a Results Table containing only the standard.

2. Use the Peak Review pane to make sure that the integration was successful.

3. Use the Export Calibration command to save a copy of the calibration.

4. Create a new Results Table containing samples of unknown concentration.

5. Click Import External Calibration to apply the exported calibration equation to the new Results Table.

Note: Users can also specify the calibration file (*.mqcal) to apply to the new Results Table.

6. Repeat steps 4 and 5, as required.

If changes are made to the original Results Table (with the standard samples), then the Results Table must beexported again to save the updated calibration equation. Previously exported calibrations are not automaticallyupdated.

Regression Types

The area of the analyte peaks in the calibration curve standards is plotted against the known concentrations.Subsequently, a line is fitted to the points. This regression line is used to calculate the concentration of the unknownsamples.

In the Analytics workspace, the following types of regression are available for the calibration curve:

• Linear (y = mx + b)

• Linear through Zero (y = mx)

• Mean Response Factor



• Quadratic (y = a2 + bx + c)

• Power

• Wagner

• Hill

As well, it is possible to add different types of weighting for the regression, including:

• None

• 1/x

• 1/x2

• 1/y

• 1/y2

• ln(x)

• ln(y)

Analyzing Data Using Metric PlotsUse a metric plot to plot the values in a Results Table column against either the row number or another column.These plots are a valuable aid for visual data review.

If one column is selected, the resulting plot shows the values from the column as a function of the row numberin the table. If two columns are selected, then the values from the columns are plotted against one another. Thefirst of the two columns to be selected contains the x values and the second the y values.


2. Open a Results Table.

3. Select one or two columns.

4. Click More > Create Metric Plot with new settings.

5. In the metric plot, click Link and then click Link to results table columns or Link to results tablerows to link the scrolling in the Results Table to the metric plot.

6. Click Options and then use the following features as required:



Table 6-25 Metric Plot Right-Click Menu Options

DescriptionMenu Option

Use the dialog to select the regression model. Refer to the Help system for moreinformation.

Regression

When this option is selected, plots values that are not numerical using a y-value ofzero. Otherwise, such points are omitted from the plot. For example, the RetentionTime is reported as N/A for peaks that could not be integrated. For this feature, a pointis present for such peaks so that the user can see these potentially problematic samplesand then link them to the Peak Review pane by clicking the point.

Display “N/A” as 0.0

Changes whether the data points are labeled using the text from the Sample Namefield of the Results Table. If there is more than one overlaid trace, then only thecurrently active trace is labeled.

Show sample names

Changes the legend that annotates the point symbols used for the various sample types.Show legend

Changes whether the y-axis uses absolute units or a percentage of the maximum y-value.When using the percentage feature, the percentage is calculated independently foreach overlaid trace. This feature can be used to plot overlaid traces for multiplecomponents and the response for the metric for the components is significantly different.

Use percent Y-axis

Changes whether the y-axis starts at y=0 or at the minimum y-value needing to beplotted.

Start Y-Axis at zero

Changes whether the data points are connected by lines.Connect with lines

If the plot is currently associated with a setting, then this feature saves the currentfeatures. Otherwise, this feature behaves the same as the Save Setting As feature.

Save setting

If the same columns are frequently plotted, then the user can save the plotting optionsas a setting. This enables the user to quickly generate a plot even if the required columnsare not currently visible in the Results Table. In addition to the columns, the variousplotting options are saved. After a setting is saved, the name is shown in the MetricPlot menu.

Save setting as

If the current plot is associated with a setting, then use this feature to delete the setting.Delete setting

Metric Plot Tips

• If users left-click on a data point, then the corresponding row of the Results Table is automatically selectedand scrolled into view. If the Peak Review pane is open, then it also updates to show the correspondingchromatogram. This provides a convenient means of performing peak review for outliers.



• The title region always shows the name of the active trace. If traces for multiple components are overlaid, thentoggle the title between showing information for all of the traces or just the active one by double-clickinganywhere within the title region. Activate a particular trace by clicking the color spot to the left of thecorresponding title.

Audit TrailsUsers can view the audit trail records for each Results Table.

View The Audit Trail Records in the Audit Trail Viewer


2. Click Views > Audit trail viewer.

3. Open a session file.

Note: Click the Project list and then select another project to change projects to view audit trail for theresult tables under different project.

4. To view records for other Results Tables, click the Sessions list and then select another file.

Tip! The user can also select to view all of the Results Tables in the project at the same time.

Filter Audited Events Using a Keyword Search

The user can filter the audited events in the audit trail using a keyword search, which highlights every occurrenceof the text.




4. Type the word to find in the Find field.

5. Click Go.

If matches are found, then the Find field turns green, the number of matches is shown, and the word ishighlighted in yellow. If matches are not found, then the Find field turns pink.

6. Use the Next and Prev buttons to move through the matches.

Filter Audited Events using a Set of Specified Criteria

The user can filter the audited events in the audit trail based on a set of specified criteria.






4. Click Filter.

The Filter Audit Trail Events dialog opens.

5. Use the lists to select the required filter criteria.

Figure 6-57 Filter Audit Trail Events Dialog


Use to filter on a specific word or phrase.is1

Use to filter on a partial word or phrase.contains2

Name of the Results Table (.session) file. The user can filter onefile or all of the files for the active project.

N/A3




Select from the list and then type the following, as required:• Type the partial or full event type.

• Type the partial or full sample name.

• Type the partial or full name of the user.

• Select Yes or No.

• Type a reason.

And where• Description

• Sample Name

• Full User Name

• Notification

• Reason

4

Filter on events that occurred during a specific date and time.And where time and dateare

5

Note: The Results Table field is not editable.

6. Click Clear to reset all of the filter criteria to No filter.

7. Click OK to filter the events.

Tip! Click Remove Filter in the Audit Trail Viewer dialog to remove the filter.

Print the Audit Trail Viewer




4. Click Print.

5. Select a printer.

Note: Only the saved events portion of the Audit Trail Viewer dialog are printed.

Change the Column Settings in the Audit Trail Viewer




4. Click Column Settings.



5. Select or clear the columns as required in the Column Settings dialog. Refer to Select Columns for the ResultsTable on page 154.

Integration Algorithm Parameters

MQ4 Integration Algorithm ParametersThe following parameters are used to identify and report the peak of interest. Refer to Integration AlgorithmParameters on page 186 for a complete list of available parameters.

Noise Percentage

This parameter is used to estimate the noise level in the chromatograms. The specified percentage of the datapoints with the smallest intensity are assumed to be noise.

Typical values range from 20% to 60%. If small peaks in the presence of larger peaks are not being found, thenthe noise percentage should be lowered. Figure 6-58 is an example of a small peak in the presence of an extremelylarge peak. This peak is not found when the noise percentage is set to 90% but is found when the noise percentageis set to 40%.

Figure 6-58 Peak of Interest

In Figure 6-59, the left graph shows the noise percentage set to 40%. The right graph is set to 90%.



Figure 6-59 Noise Levels

Baseline Sub. Window

After smoothing, but before other processing, chromatograms are baseline subtracted to remove humps in thedata. For each data point, the baseline is calculated using the data points on both the left and right side of thecurrent point with minimum intensity (within the subtraction window).

The exact value of this parameter is not critical, provided that it is set at least a few times larger than the expectedpeak width.

In Figure 6-60, the left graph shows the Baseline Sub. Window set to 0.1 minutes and the right graph shows theBaseline Sub. Window set to 1 minute.

Figure 6-60 Baseline Subtraction Window



Peak Splitting

This parameter controls whether a potentially noisy peak is found as one single peak or as two (or more) separatepeaks. If the dip between two potential peaks is less than the specified value, then a single peak is found. Otherwise,two peaks are found.

Setting this parameter to a large value will prevent noisy peaks from being split and found as two separate peaks.However, a smaller value needs to be used if there are two closely eluting (overlapping) distinct peaks.

In Figure 6-61, the graph on the left shows Peak Splitting set to two points. The graph on the right shows PeakSplitting set to three points.

Figure 6-61 Peak Splitting

AutoPeak Integration Algorithm ParametersThe following parameters are used to identify and report the peak of interest.

For more information, refer to the Help system.

• Local peak baseline: The software assesses changes to the baseline locally around the peak as opposedto calculating the baseline with respect to the entire chromatogram.

• Linear peak baseline: The software fits a line between the points at the beginning and at the end of thatspecific group of peaks as opposed to the possibility of having a non-linear as the baseline below the peak.

Saturation correction: When the algorithm detects that a peak is saturated, it uses the model to predict howthe peak might look if the detector had not saturated. This causes the profile to extend above the top of the peakto approximate the response that would have been obtained if the detector had not saturated. This can extendthe linear dynamic range of calibration curves. This option is only available when setting the overall algorithmdefault values and not during processing method creation or individual peak review, because it is not useful touse this setting for only some peaks.



Edit Report Templates

CAUTION: Potential Data Loss. To prevent users from modifying templates, make sure thatthe Reporter templates are located in secured, read-only folders that are accessible forwriting only by system administrators.

In the event of creating a custom template, the user is responsible for validating the template.

1. Open the .docx template.

The Reporter template editor opens on the right. The template editor is automatically populated with the taginformation.

Figure 6-62 Reporter Template Editor

DescriptionItem

Report template showing the current tags.1

Icons:

• Add new tag.

• Add picture tag.

• Show content area.

• View document change log.

2



DescriptionItem

Tags for: Shows the name of the software providing the tag information.3

Field Type: Shows the field types applicable to the software.4

Shows a list of available attributes based on the selected field type. For example tagname and number format.

5

Save Tag Parameters: Click to save changes. If changes are not saved, a message isshown prompting the user to save the changes.

6

2. Use the procedures in Table 6-26.

3. Click Save Tag Parameters after any changes are made.

Tip! Mandatory information is indicated by a flashing red exclamation sign at the left of the field.

Table 6-26 Reporter Functions

...do thisTo do this...

Click inside the tag, select a new field type and then select the attributes.Change the field type.

Click inside the tab and then change the attributes as required.Change the attributes of the fieldtype.

Click the Add new tag icon, select the Field Type, and then select theattributes.

Add a tag.

Click the Add picture tag icon and then select the attributes.Add a picture.

Click the Show content area icon.Show where a tag starts and ends.

Click the View document change log icon.Show the document audit log.

Paste the selected tags in the new location and then update the fieldtype attributes.

The attributes are not copied and must be selected.

Copy tags.

Use the left and right arrow keys to move between the tags.Navigate between the tags.

Do one of the following:

• If the cursor is to the left of the tag, press Delete.

• If the cursor is to the right of the tag, press Backspace.

Delete tags.



Reporter TemplatesIt is the responsibility of the user to validate the custom report template.

Some report templates use queries. Users can create queries using Microsoft Excel-based formulae to evaluate,manipulate, and present the data from the Results Table in a report. The Metafield tag in the report template tellsthe report the name of the query file that it should use. To use queries, the name of the query file must be specifiedin the MetaField tag in the report template. Queries must also have the extension ".query" to be recognized as aquery. The queries must be stored in the Reporter folder where the report templates are stored.

We recommend that the user validate the generated results when a Reporter template is used, especially whenqueries are used in a template. If any modifications are made to the report template after validation, then thereport template should be re-validated. Changes to the report template include any modification to reporter tagsor queries.

Table 6-27 Reporter Template Descriptions

DescriptionTemplate

A report showing, for each sample, a section including the File Information, SampleInformation, Analyte Results Table, and overlaid chromatograms of all of the analytes andinternal standard. The Analyte Results table is printed as shown in the Results Table. Allthe qualitative confidence traffic lights are listed at the beginning of the table.

All Peaks Qual

A report showing the File Information for each analyte and an XIC table for each Blank,each Standard, each QC, and 20% of the unknown samples. Unknown samples are selectedby the user-defined criteria in the report query.

Analyte 20 percent

A report showing, for each analyte, a section of the Samples Summary Table.Analyte Summary

A report showing the File Information, Statistics Table (standards), and Calibration Curvefor analytes, one page per analyte.

Calibration Curves

A report showing, for each analyte, a section including the File Information and a metricplot of the analyte peak area.

Metric Plot

A report showing, for each selected sample, a section including the File Information,Sample Information, and Analyte Results Table for the selected analytes. The AnalyteResults table is printed as shown in the Results Table. All the qualitative confidence trafficlights are listed at the beginning of the table.

Per SampleQuant-Qual

A report showing, for each selected sample, a section including the File Information,Sample Information, and Analyte Results Table for the selected analytes. The AnalyteResults table is printed as shown in the Results Table. All the qualitative confidence trafficlights are listed at the beginning of the table.

Per SampleQuant-Qual VisibleRows Using VisibleAnalyte



Table 6-27 Reporter Template Descriptions (continued)

DescriptionTemplate

A report showing, for each analyte, a section including the File Information, Results Table,Calibration Curves, and chromatograms including the internal standard and each analyte.This template is suitable for a Results Table with a group defined in it.

Per AnalyteQuant-Qual

A report showing, for each sample, a section including the File Information, SampleInformation, Analyte Results Table, Calibration Curves for each analyte, and chromatogramsincluding the internal standard and each analyte. This template is suitable for a ResultsTable with a group defined in it.

Per Sample Report

A report showing, for each selected sample, a section including the File Information;Sample Information; Analyte Results Table for the selected analytes; overlaidchromatograms of all of the analytes, internal standard, and the XIC; the Acquired/Theoretical MS spectra; and the Acquired/Library MS/MS spectra for each selected analyte.The Analyte Results table is printed as shown in the Results Table. All the qualitativeconfidence traffic lights are listed at the beginning of the table.

Positive Hits Qual

A report in .csv format showing, for each sample, a section including the File Information,Sample Information, and Analyte Results Table.

Qual CSV report

A report showing, for each sample, a section of Analytes Summary Table. This reporttemplate is suitable for a Results Table with groups.

Sample Summary

MS TuneA .dat file is created by the software when the instrument data is saved. Use this file to restore earlier parameterstates. The .dat backup file is named using the time that the file was created, not the time that the file was backedup.

Note: Instrument optimization should be performed using the ESI probe only.

Each time the user loads the MS Tune procedure, all of the mass spectrometer parameters are backed up.

Perform a Quick Status CheckUse this procedure to calibrate the system and to quickly verify the resolution in TOF MS and MS/MS modes. Ifthe channel alignment mass accuracy does not meet the specification, then the user can repeat the steps andcalibrate the system. If the resolution does not meet the specification, then the user can perform the TOF Tuningprocedure to optimize the system.

Tip! Users can assess the this procedure by clicking MS Check on the status panel.



1. Open the MS Tune workspace.

2. Select Positive Quick Status Check or Negative Quick Status Check from the Tuning Procedureslist.

3. Double-click the CDS power icon ( ) on the status panel to turn on the CDS flow.

4. Select the correct channel, 1 or 2, click Start, and then close the window.

5. Wait at least 1 minute for the CDS to equilibrate.

6. Click Next.

7. Follow the on-screen instructions for each step.

8. (Optional ) Review the report to verify the results of each step.

9. (Optional) Save the report.

10. Click Save Tuning Settings if the results are satisfactory. If the results are not satisfactory, then do one ofthe following:

• Repeat the steps.

• Run the TOF MS tuning procedure. Refer to Tune TOF MS on page 194.

• Discard the results by closing the MS Tune workspace.

• Restore the previous settings by selecting the appropriate backup file from the Restore InstrumentData menu.

Optimize the DetectorWhen the system sensitivity is low, use this procedure to verify that the detector voltage is optimized. During theprocedure, the software can adjust the detector voltage to provide the optimum sensitivity. When the optimizationis completed, the user can save the optimized value or discard the changes.

We recommend optimizing the detector every 6 months, or when the signal diminishes or is lost after cleaning.


2. Select Detector Optimization from the Tuning Procedures list.

3. Make sure that the spray is stable.

4. Click Next.

5. Follow the on-screen instructions.

6. Click Next.

The optimization report is shown.




8. Click Next.

9. Click Save Settings.

Note: If the detector optimizes at 2650 V or higher, then contact sciex.com/request-support support toreplace the detector.

Tune Q1In MS/MS experiments, the Q1 region is used to select a precursor ion for fragmentation. Q1 Unit tuning optimizesthe peak width and calibrates the Q1 mass. Q1 Unit represents the width of the precursor ion selection windowat unit resolution. Q1 Low or Open represents the width of the precursor ion selection window at Low resolution(wider window ) or Open resolution (open window ). After the Q1 Unit is tuned, Q1 Low and Open settings arecalculated based on the Q1 Unit values.


2. Select Positive Q1 Tuning or Negative Q1 Tuning from the Tuning Procedures list.





7. Click Next.


9. (Optional) Click Edit Method to adjust the parameters.

10. If calibration was performed, then click Confirm to run a confirmation acquisition.

11. Click Next.


13. Click Next.


Tune TOF MSThe TOF MS Tuning procedure optimizes the parameters for resolution and sensitivity in TOF MS and MS/MSmodes. The optimization starts verifying the system performance before tuning, and then ramps various parametersfor maximum intensity and resolution. After channel alignment, the system is calibrated and the system performanceis determined. If the performance is satisfactory, then the user can save the tuning settings to the system or discardthe settings.




TOF MS tuning can be performed in automatic or manual mode. In manual mode, users can select the optimizedparameter values or pause at the end of the tuning steps.


2. Select Positive TOF MS Tuning or Negative TOF MS Tuning from the Tuning Procedures list.





7. Click Next.


9. Click Next.


11. Click Save Settings if the results are satisfactory. If the results are not satisfactory, then do one of thefollowing:

• Repeat the steps.

• Discard the results by closing the MS Tune workspace.

• Restore the previous settings by selecting the appropriate backup file from the Restore InstrumentData menu.

• Contact sciex.com/request-support.

Tune Q1 HighIn MS/MS experiments, the Q1 region is used to select a precursor ion for fragmentation. Q1 High tuning optimizesthe peak width and calibrates the Q1 mass. Q1 High represents the width of the precursor ion selection windowat high resolution.


2. Select Positive Q1 High Tuning or Negative Q1 High Tuning from the Tuning Procedures list.

Note: If the positive Q1 High procedure has not been run for a period of time, then click Copy to use thePositive Q1 Unit settings as a starting point.








7. Click Next.


9. (Optional) Click Edit Method to adjust the parameters.

10. If calibration was performed, then click Confirm to run a confirmation acquisition.

11. Click Next.


13. Click Next.


Perform Advanced TroubleshootingIf the tuning procedure results are not satisfactory, then use this advanced troubleshooting procedure to optimizethe parameters related to the mass spectrometer. Users can also view the TDC channel statistics and spectra duringacquisition.

Tip! The Live Method window can be used to view the optimized parameters after tuning is performed.


2. Select Advanced Troubleshooting from the Tuning Procedures list.

3. Select a scan type.

4. Click Edit Method and then edit the parameters in the Live Window window, as required.

5. Click Start/Restart Method.

6. View the data and then adjust the parameters, as required.

7. Click Stop and then save the detector parameters or the TOF MS parameters, as required.

Restore Instrument DataThe software generates a copy of the instrument data file ( .dat ) and then updates the current .dat file wheneverthe user saves the tuning settings at the end of each tuning procedure. Previously saved settings can be restoredusing the Restore Instrument Data feature.

When each tuning procedure is performed, the report and data files are generated to track the optimized results.The .wiff2 data file and report can be found at D:\SCIEX OS Data\Optimization.


2. From the Restore Instrument Data list, select a data file.



Figure 6-63 Instrument Tuning and Optimization Dialog

3. (Optional) Click View Report.

4. Click Yes.

Event Log WorkspaceThe Event Log workspace contains logs of system events including errors, warnings, and messages. This informationmight be helpful in troubleshooting and performing system diagnostics.

View Logs

1. Open the Event Log workspace.

2. Click an item from the list in the left panel to view the logs.

Print Logs


2. (Optional) Open an archived log.

3. Click Print.

Archive Logs


2. Click Archive > Archive Log.



Figure 6-64 Archive > Archive Log

The Archive Log dialog opens.

Figure 6-65 Archive Log Dialog

3. In the Archive event log items older than field, click the date icon and then select a date.

4. Click Archive.



Regularly clean and maintain the system for optimal performance.



Recommended Maintenance ScheduleTable 7-1 provides a recommended schedule for cleaning and maintaining the system.

Tip! Perform maintenance tasks regularly to make sure that the mass spectrometer is performing optimally.

For information on maintaining the ion source, refer to the ion source Operator Guide.

Contact a Qualified Maintenance Person (QMP) to order consumable parts. Contact a SCIEX Field Service Employee(FSE) for maintenance service and support.

Table 7-1 Maintenance Tasks

For more information...TaskFrequencyComponent

System

Refer to Chemical Precautions on page11.

Inspect the tubingand fittings to makesure that they aresecurely connected,and that there areno leaks.

DailyTubing


7Service and MaintenanceInformation

Table 7-1 Maintenance Tasks (continued)


Mass Spectrometer

Refer to Clean the Curtain Plate onpage 206.

CleanDailyCurtain plate

Refer to Clean the Front of the OrificePlate on page 207.

CleanDailyOrifice plate (front)

Refer to Inspect the Roughing Pump OilLevel on page 211.

Inspect the levelWeeklyRoughing pump oil

Contact the local QMP or FSE.ReplaceEvery three years or as neededRoughing pump oil

Refer to Clean the Surfaces on page201.

CleanAs neededInstrumentsurfaces

Refer to Empty the Source ExhaustDrain Bottle on page 207.

EmptyAs neededSource exhaustdrain bottle

Contact the local QMP or FSE.CleanAs neededOrifice plate (frontand rear)

Contact the local QMP or FSE.CleanAs neededQJet® ion guide

and IQ0 lens

Contact the local QMP or FSE.CleanAs neededQ0 rod set and IQ1lens

Contact the local QMP or FSE.RefillAs neededRoughing pump oil

Contact the local QMP or FSE.ReplaceAs neededInterface heater

Refer to Replace the CDS Bottle onpage 41.

Replace or refillAs neededCDS bottle

Refer to Replace the Check Valve andFlow Module on page 210.

ReplaceAs neededCDS flow module

Ion Source

Refer to the ion source OperatorGuide.

Inspect and replaceAs neededTwin ESI or twinAPCI electrodes


ReplaceAs neededCorona dischargeneedle


Service and Maintenance Information

Table 7-1 Maintenance Tasks (continued)


Contact the local QMP or FSE.ReplaceAs neededTurbo heater


ReplaceAs neededSample tubing

For “As needed” tasks, follow these guidelines:

• Clean the mass spectrometer surfaces after a spill or when they become dirty.

• Empty the drain bottle before it becomes full.

• Clean the orifice plate, QJet® ion guide, and Q0 region if system sensitivity degrades.

Tip! Clean the Q0 region regularly to minimize the impact of charging (a significant loss of sensitivity of theions of interest over a short period of time) on the quadrupoles and lenses. Contact a QMP or FSE.

• Clean the QJet® ion guide and Q0 region if system sensitivity degrades.

Tip! Clean the Q0 region regularly to minimize the impact of charging (a significant loss of sensitivity of theions of interest over a short period of time) on the quadrupoles and lenses. Contact a QMP or FSE.

• Refill the roughing pump oil when it falls below the minimum oil level.

Clean the SurfacesClean the external surfaces of the mass spectrometer after a spill or when they become dirty.

CAUTION: Potential System Damage. Use only the recommended cleaning methods andmaterials to avoid damaging the equipment.

1. Wipe the external surfaces with a soft cloth dampened with warm, soapy water.

2. Wipe the external surfaces with a soft cloth moistened with water to remove any soap residue.

Clean the Front-EndThe following warning applies to all of the procedures in this section:



WARNING! Hot Surface Hazard. Let the ion source cool for at least 30 minutes beforestarting any maintenance procedures. Surfaces of the ion source become hot duringoperation.

Clean the mass spectrometer front-end using the routine cleaning method, to:

• Minimize unscheduled system downtime.

• Maintain optimum sensitivity.

• Avoid more extensive cleaning that requires a service visit.

When contamination occurs, perform an initial routine cleaning. Clean up to and including the front of the orificeplate. If routine cleaning does not resolve issues with sensitivity, then a full cleaning might be necessary. Contactthe local QMP or FSE.

This section provides instructions for performing routine cleaning without breaking vacuum.

Note: Follow all of the applicable local regulations. For health and safety guidelines, refer to Chemical Precautionson page 11.

Symptoms of ContaminationThe system might be contaminated if any one of the following is observed:

• Significant loss in sensitivity

• Increased background noise

• Additional peaks that are not part of the sample are shown in full scan or survey scan methods

If any of these issues are observed, then clean the mass spectrometer front-end.

Required Materials

Note: U.S. customers can call 877-740-2129 for ordering information and inquiries. International customerscan visit sciex.com/contact-us.

• Powder-free gloves (nitrile or neoprene recommended)

• Safety glasses

• Laboratory coat

• Fresh, high-quality (pure) water (at least 18 MΩ de-ionized [DI] water or ultra-pure HPLC-grade water). Oldwater can contain contaminants that can further contaminate the mass spectrometer.

• MS-grade methanol, isopropanol (2-propanol), or acetonitrile




• Cleaning solution. Use one of:

• 100% methanol

• 100% isopropanol

• 1:1 acetonitrile:water solution (freshly prepared)

• 1:1 acetonitrile:water with 0.1% acetic acid solution (freshly prepared)

• Clean 1 L or 500 mL glass beaker to prepare cleaning solutions

• 1 L beaker to catch used solvent

• Organic waste container

• Lint-free wipes. Refer to Tools and Supplies Available from the Manufacturer on page 203.

• (Optional) Polyester (poly) swabs

Tools and Supplies Available from the Manufacturer

Part NumberDescription

1017396Small poly swab (thermally bonded). Also available in the Cleaning kit.

018027Lint-free wipe (11 cm x 21 cm, 4.3 inches x 8.3 inches). Also available in the Cleaningkit.

Cleaning Best Practices

WARNING! Hot Surface Hazard. Let the ion source cool for at least 30 minutes beforestarting any maintenance procedures. Surfaces of the ion source and the vacuuminterface components become hot during operation.

WARNING! Toxic Chemical Hazard. Refer to the chemical product Safety Data Sheetsand follow all of the recommended safety procedures when handling, storing, anddisposing of chemicals. For health and safety precautions, refer to the System UserGuide.





• Allow the ion source to cool before removing it.

• Always wear clean, powder-free gloves (nitrile or neoprene recommended) for the cleaning procedures.

• After cleaning the mass spectrometer components, and before reassembling them, put on a new, clean pairof gloves.

• Do not use cleaning supplies other than those specified in this procedure.

• If possible, prepare cleaning solutions just before cleaning.

• Prepare and store all of the organic solutions and organic-containing solutions in very clean glassware only.Never use plastic bottles. Contaminants can leach from these bottles and further contaminate the massspectrometer.

• To avoid contaminating the cleaning solution, pour the solution on the wipe or swab.

• Allow only the center area of the wipe to contact the mass spectrometer surface. Cut edges can leave fibersbehind.

Tip! Wrap the wipe around a thermally-bonded poly swab.

Figure 7-1 Example: Folding the Wipe

• To avoid cross-contamination, discard the wipe or swab after it has touched the surface once.

• Larger parts of the vacuum interface, such as the curtain plate, might require several cleanings, using multiplewipes.

• Only dampen the wipe or swab slightly when applying water or cleaning solution. Water, more often thanorganic solvents, might cause the wipe to deteriorate, leaving residue on the mass spectrometer.

• Do not rub the wipe across the aperture. Wipe around the aperture to prevent fibers from the wipes fromentering the mass spectrometer.

• Do not insert the brush in the aperture on the curtain plate or orifice plate.



Prepare the Mass Spectrometer

WARNING! Hot Surface Hazard. Let the ion source and vacuum interface cool for atleast 30 minutes before starting any maintenance procedures. Some surfaces of theion source and vacuum interface become hot during operation.

CAUTION: Potential System Damage. Do not drop anything into the source drain when theion source is removed.

Figure 7-2 Source Drain on the Vacuum Interface

1. Deactivate the devices. Refer to Deactivate Devices on page 46.

2. Remove the ion source. Refer to the ion source Operator Guide.

When the ion source is not in use, store it to protect it from damage and to maintain operating integrity.



Clean the Curtain Plate

CAUTION: Potential System Damage. Do not rest the curtain plate or orifice plate on theaperture tip. Make sure that the conical side of the curtain plate faces up.

CAUTION: Potential System Damage. Do not insert a wire or metal brush into the apertureon the curtain plate, orifice plate, or interface heater to avoid damaging the aperture.

1. Pull the curtain plate off of the vacuum interface and then put it, conical side up, on a clean, stable surface.

Figure 7-3 Curtain Plate Removal

The curtain plate is held in place by three retaining ball catches mounted on the orifice plate.

Tip! If the curtain plate does not immediately separate from the orifice plate, then turn the curtain plateslightly (less than 90 degrees) to release the ball spring latches.

2. Dampen a lint-free wipe with pure water and then clean both sides of the curtain plate.

Note: Use multiple wipes, as required.

3. Repeat step 2 using the cleaning solution.

4. Using a dampened wipe or small poly swab, clean the aperture.

5. Wait until the curtain plate is dry.

6. Inspect the curtain plate for solvent stains or lint, removing any residue with a clean, slightly damp, lint-freewipe.



Note: Persistent spotting or filming is an indicator of contaminated solvent.

Clean the Front of the Orifice Plate

CAUTION: Potential System Damage. When cleaning the surface of the orifice plate, donot remove the interface heater. Frequent removal of the interface heater can result indamage to the interface heater. Surface cleaning of the interface heater is adequate forroutine cleaning.

CAUTION: Potential System Damage. Do not insert a wire or metal brush into the apertureon the curtain plate, orifice plate, or interface heater to avoid damaging the aperture.

1. Dampen a lint-free wipe with water and then wipe the front of the orifice plate, including the interface heater.

2. Repeat step 1 using the cleaning solution.

3. Wait until the orifice plate is dry.

4. Inspect the orifice plate for solvent stains or lint, removing any residue with a clean, slightly damp, lint-freewipe.

Note: Persistent spotting or filming is an indicator of contaminated solvent.

Put the Mass Spectrometer Back in Service

1. Install the curtain plate on the mass spectrometer.

2. Install the ion source on the mass spectrometer. Refer to the ion source Operator Guide.

Tighten the ion source by turning the source latches down into the locking position.

3. Click Activate Devices on the status panel in the SCIEX OS software.

Empty the Source Exhaust Drain Bottle

WARNING! Radiation Hazard, Biohazard, or Toxic Chemical Hazard. Deposithazardous materials in appropriately labeled waste containers and disposeof them according to local regulations.



WARNING! Radiation Hazard, Biohazard, or Toxic Chemical Hazard. Take careto vent exhaust gases to a dedicated laboratory fume hood or exhaust systemand make sure that the ventilation tubing is secured with clamps. Make surethat the laboratory has appropriate air exchange for the work performed.

Inspect the source exhaust drain bottle regularly, and empty it before it becomes full. Also inspect the bottle andits fitting for leaks, and tighten connections or replace components, if required. Follow the steps in this procedureto empty the bottle.

1. Remove the ion source. Refer to the ion source Operator Guide.

2. Loosen the clamps connecting the hoses to the cap of the source exhaust drain bottle.

3. Disconnect the hoses from the cap.

4. If applicable, lift the drain bottle out of the holder.

5. Remove the cap from the drain bottle.

6. Empty the drain bottle and then dispose of the waste according to laboratory procedures and local wasteregulations.

7. Install the cap on the bottle and then put the bottle in the holder.

8. Attach the hoses to the cap and then secure them tightly with clamps.



Figure 7-4 Source Exhaust Drain Bottle

DescriptionItem

Connection to vent1

Source exhaust drain tubing: 2.5 cm (1.0 inch) inside diameter (i.d.)2

Roughing pump exhaust hose: 3.2 cm (1.25 inch) i.d.3

Source exhaust drain bottle. Make sure that the bottle is secured to prevent spillage.4

Connection to the mass spectrometer: 1.6 cm (0.625 inch) i.d.5

Roughing pump vacuum inlet hose6

Note: Source exhaust hose connections at the drain bottle, mass spectrometer, and the lab vent are securedwith hose clamps.



Replace the Check Valve and Flow Module


The check valve prevents calibrant from flowing into the ion source when the CDS is off. The flow module is adimension-critical 10 cm length of black tubing that controls the flow rate of the calibrant into the ion source.

Figure 7-5 Check Valve and Flow Module

DescriptionItem

To the CDS1

Check valve2

Flow module3

To the ion source4

Required Materials

• 1/4 inch wrench

1. To remove the check valve, loosen the finger-tight PEEK fittings on both sides of the check valve.

Note: When installing the check valve, make sure that the arrow on the check valve points toward the ionsource.



2. To remove the flow module, follow these steps:

a. Loosen the finger-tight PEEK fitting that connects the flow module to the check valve.

b. Use a 1/4 wrench to remove the fitting that connects the flow module to the probe.

Inspect the Roughing Pump Oil Level

• Inspect the sight glass on the roughing pump to verify that the oil is above the minimum level.

If the oil is below the minimum level, then contact the qualified maintenance person (QMP) or SCIEX fieldservice employee (FSE).



Figure 7-6 Sight Glass

Storage and Handling


If the mass spectrometer must be stored for a long time or prepared for shipping, then contact a SCIEX FSE fordecommissioning information. To disconnect power from the mass spectrometer, remove the mains supply connectorfrom the AC mains supply.



Note: The system must be transported and stored between –30 °C to +60 °C (–22 °F to 140 °F). Store thesystem at an altitude not exceeding m ( feet) above sea level.

Move the Mass Spectrometer

WARNING! Lifting Hazard. Make sure that at least nine people for X500R or tenpeople for X500B are available to lift the mass spectrometer. Follow establishedsafe lifting procedures. Refer to the Site Planning Guide for the weights of systemcomponents.

WARNING! Lifting Hazard. Make sure that at least two people are available to liftthe roughing pump. Follow established safe lifting procedures.

WARNING! Hot Surface Hazard. Beware of burns. Surfaces of the mass spectrometerbecome hot during operation.

Prerequisites

• Shut down the system. It is not necessary to vent the system. Refer to Shut Down and Vent the System onpage 37.

• Turn off all of the gas flows and then relieve the pressure in the gas lines.

Required Materials

• Lifting kit

1. Disconnect the vacuum hose, gas tubing, source exhaust tubing, power cable, ethernet cable, and TDC cablefrom the mass spectrometer.

2. Remove the left and right skirts.

3. On the right front side of the mass spectrometer, pull out the locking pin that secures the lifting bar, pull outthe bar until the hole in the bar lines up with the hole in the tube, and then secure the bar with the lockingpin.



Figure 7-7 Lifting Bar Retracted

Figure 7-8 Lifting Bar Extended

4. Repeat step 3 at the right back, left front, and left back of the mass spectrometer.

5. Install a short block on each lifting bar, and then secure it with a locking pin.

CAUTION: Potential System Damage. Make sure that all locking pins are fully inserted,to avoid dropping the mass spectrometer while it is being moved.



Figure 7-9 Short Block Installed

6. On the right side of the mass spectrometer, insert a long rod through the blocks.

Note: The end of the bar with the longest extension past the block must be at the front of the massspectrometer.

7. Repeat step 6 on the left side of the mass spectrometer.

8. Install the locking pins in the long rods.



Figure 7-10 Installing the Locking Pin on the Log Rod

9. Install the tall blocks on the ends of the long rods, and then secure them with two locking pins.

Figure 7-11 Tall Block Installed

10. At the front of the mass spectrometer, insert a short rod through the tall blocks.

11. Secure the short rods with two locking pins.



Figure 7-12 Installing the Locking Pin on the Short Rod

Figure 7-13 Lifting Kit Installed (X500R System)



12. With the assistance of eight additional people, for X500R systems, or nine additional people, for X500B systems,move the mass spectrometer to the new location.

Figure 7-14 shows the position of the 10 people required to lift the X500B system. The person designated as10 is at the front of the system, and must move aside to allow the system to be taken off and put onto thebench. For X500R systems, only positions 1 through 9 are required.

Figure 7-14 Distribution of Operators (X500B System)

13. With the assistance of one additional person, move the roughing pump to the new location.

14. Install the left and right skirts.

15. Connect the vacuum hose, gas tubing, source exhaust tubing, power cable, ethernet cable, and TDC cable tothe mass spectrometer.



CAUTION: Potential System Damage. Make sure that the vacuum hose clamp is orientedso that it does not protrude past the side of the mass spectrometer. If it is orientedincorrectly, it might damage the dress panel when the dress panel is opened to servicethe mass spectrometer.

Figure 7-15 Correctly Installed Clamp

Generate a Support Package


2. Click About in the left panel.

3. Under Service and Support, click Generate a Support Package.

The zipped report is saved to the D:\ServicePackages folder.

4. Send the zip file to support.



This section contains information for troubleshooting basic system issues. Certain activities can only be carriedout by a SCIEX -trained Qualified Maintenance Person (QMP) in the laboratory. For advanced troubleshooting,contact a SCIEX Field Service Employee (FSE).

Table 8-1 System Issues

Corrective ActionPossible CauseSymptom

The Curtain GasTM flow rate is toolow.

The QJet® ion guide is extremely dirty

or frequently becomes dirty.

1. Inspect the roughing pump oillevel, and then contact the localQMP or an FSE to add oil.

2. Inspect and repair leaks.

3. Install the correct orifice plate.

1. The roughing pump oil level istoo low.

2. There is a leak.

3. The wrong orifice plate isinstalled.

A system fault has occurred becausethe vacuum pressure is too high.

Contact the local QMP or FSE.1. Ambient temperature is too high.A system fault has occurred becausethe QPS exciter module temperatureis too high.

1. Confirm the fault in the Statuspanel of the device details page.

2. Install the probe. Refer to the ionsource Operator Guide.

3. Remove and replace the probe.Tighten the retaining ringsecurely. Refer to the ion sourceOperator Guide.

1. The probe is not installed.

2. The probe is not connectedsecurely.

The SCIEX OS software reports thatthe mass spectrometer is in Faultstatus because of the ion source.

Contact an FSE.The F3 fuse is blown.The SCIEX OS software indicates thatthe APCI probe is in use, but theTurboIonSpray

® probe is installed.

Clean or replace the electrode. Referto the ion source Operator Guide.

The electrode is blocked.The spray is not uniform.


8Mass SpectrometerTroubleshooting

Table 8-1 System Issues (continued)


1. Optimize the ion sourceparameters. Refer to theSCIEXOS software Help system.

2. Refer to Clean the Curtain Plateon page 206.

3. Refer to Clean the Front of theOrifice Plate on page 207 orcontact the local QMP or FSE.

4. Clean the Q0 region. Contact theQMP or FSE.

5. Inspect the syringe or sample linefor leaks, and repair any leaksfound. Make sure that all fittingsare the correct type and size.

6. Verify the sample concentration.Use a fresh sample.

7. Tighten the nut that secures theelectrodes.

8. Remove and install the probe.

9. Remove and install the ionsource, making sure that thelatches are properly secured. Ifthis does not resolve the issue,then install and optimize analternate ion source.

10. If the O-rings are on the ionsource, then install them on thevacuum interface. If they aremissing, then contact an FSE.

11. Troubleshoot the LC system.

1. The ion source parameters arenot optimized.

2. The mass spectrometer is notoptimized.

3. The curtain plate is dirty.

4. The orifice plate is dirty.

5. The QJet® ion guide or IQ0 lens

is dirty.

6. The Q0 region is dirty.

7. The syringe or sample line isleaking.

8. The sample has degraded or hasa low concentration.

9. The nut that secures theelectrodes on the ion sourceprobe is not tight.

10. The probe is not installedproperly.

11. The ion source is not installedproperly, or it is faulty.

12. One or more of the O-rings on thevacuum interface is missing.

13. There is an issue with the LCsystem or connections.

Sensitivity is reduced.


Mass Spectrometer Troubleshooting

Table 8-1 System Issues (continued)


1. Optimize the probe. Refer to theion source Operator Guide.

2. Confirm that the sample wasprepared correctly.

3. Verify that the fittings are theright size and type and make surethat they are tight. Do notovertighten the fittings. Replacethe fittings if leaks continue.

4. Install and optimize an alternateion source.

5. Contact an FSE if the issuepersists.

1. The probe is not optimized.

2. The sample was not preparedcorrectly or the sample hasdegraded.

3. The sample inlet fittings areleaking.

The mass spectrometer performancehas degraded.

Turn the corona discharge needletoward the curtain plate, and awayfrom the stream of heater gas. Referto the ion source Operator Guide.

The position of the corona dischargeneedle is incorrect.

Arcing or sparks occur.

1. Check the CDS connections.

2. Inspect the calibrant tubing forblockages.

1. The CDS is not connected.

2. The CDS tubing is blocked.

Calibrant signal is low.

For sales, technical assistance, or service, contact an FSE or visit the SCIEX Web site at sciex.com for contactinformation.


Mass Spectrometer Troubleshooting

https://sciex.com

The following table list the standards recommended by SCIEX for calibrating the SCIEX X500 QTOF system.

Table A-1 Calibration Solutions

QuantityDescriptionPart Number

100 mLAPCI Positive Calibration Solution for the SCIEX X500 System5042914

5 × 100 mLAPCI Positive Calibration Solution for the SCIEX X500 System, 5pack

5042918

100 mLAPCI Negative Calibration Solution for the SCIEX X500 System5042915

5 × 100 mLAPCI Negative Calibration Solution for the SCIEX X500 System, 5pack

5042919

100 mLESI Positive Calibration Solution for the SCIEX X500R System5042912

5 × 100 mLESI Positive Calibration Solution for the SCIEX X500R System, 5pack

5042916

100 mLESI Positive Calibration Solution for the SCIEX X500B System5049910

5 × 100 mLESI Positive Calibration Solution for the SCIEX X500B System, 5pack

5032735

100 mLESI Negative Calibration Solution for the SCIEX X500 System5042913

5 × 100 mLESI Negative Calibration Solution for the SCIEX X500 System, 5pack

5042917

APCI Calibration IonsTable A-2 TOF MS Positive Calibration Ions

Masses

442.2647354.2122315.1623266.1598146.1176

1521.9715922.0098618.3695609.2807


ARecommended Calibration Ions

Table A-3 TOF MS Negative Calibration Ions

Masses

792.4598616.3550440.2501403.1122352.1977277.0983264.1453144.1030

Table A-4 TOF MS/MS Positive Product Ions

609.2807315.1623Precurcor Ion (m/z)

8080Declustering Potentional (V)

4527Collision Energy (V)

609.2807315.1623Fragment ion 1

577.2544270.1044Fragment ion 2

448.1966242.0731Fragment ion 3

397.2122235.1356Fragment ion 4

365.1860227.0496Fragment ion 5

236.1281220.1121Fragment ion 6

195.065286.0964Fragment ion 7

174.091358.0651Fragment ion 8

Table A-5 TOF MS/MS Negative Product Ions


–80–80Declustering Potentional (V)

–30–30Collision Energy (V)

403.1122277.0983Fragment Ion 1

277.0983249.1033Fragment Ion 2

158.0611217.0771Fragment Ion 3

125.0067200.0591Fragment Ion 4

93.0344158.0611Fragment Ion 5

N/A130.0662Fragment Ion 6


Recommended Calibration Ions

Table A-5 TOF MS/MS Negative Product Ions (continued)




ESI Calibration IonsTable A-6 TOF MS Positive Calibration Ions

Masses

829.5393609.2807442.2647354.2122315.1623266.1598132.9049

2253.83082130.24492121.93321643.86911521.97151053.9074922.0098

Table A-7 TOF MS Negative Calibration Ions

Masses

520.9100384.9352248.9604204.9706154.9738112.985668.9958

1472.73371336.75891200.78411064.8092928.8344792.8596656.8848

2233.91152165.92411880.65811633.94981565.96241744.68331608.7085

Table A-8 TOF MS/MS Positive Product Ions

829.5393609.2807315.1623Precurcor Ion (m/z)

808080Declustering Potentional(V)

454525Collision Energy (V)

829.539609.281315.162Fragment ion 1

811.529577.254270.104Fragment ion 2

724.497448.197242.073Fragment ion 3

706.486397.212235.136Fragment ion 4

607.418365.186227.05Fragment ion 5

532.334236.128220.112Fragment ion 6



Table A-8 TOF MS/MS Positive Product Ions (continued)

829.5393609.2807315.1623Precurcor Ion (m/z)

512.344195.06586.0964Fragment ion 7

494.334174.09158.0651Fragment ion 8

411.297

399.26

381.25

298.213

268.166

227.175

215.139

185.129

157.134

Table A-9 TOF MS/MS Negative Product Ions

1200.784792.8520.9384.9248.9Precurcor Ion(m/z)

8080808080DeclusteringPotentional (V)

3022201615Collision Energy(V)

1200.784792.8596520.9100384.9352248.9604Fragment Ion 1

1064.809656.8848384.9352248.9604204.9706Fragment Ion 2

928.8344520.9100248.9604204.9706154.9738Fragment Ion 3

792.8596384.9352204.9706154.9738112.9856Fragment Ion 4

656.8848248.9604154.9738112.985668.99576Fragment Ion 5

520.9100204.9706112.9856N/AN/AFragment Ion 6

384.9352154.9738N/AN/AN/AFragment Ion 7



Table A-9 TOF MS/MS Negative Product Ions (continued)

1200.784792.8520.9384.9248.9Precurcor Ion(m/z)

248.9604112.9856N/AN/AN/AFragment Ion 8

204.9706N/AN/AN/A

154.9738N/AN/AN/A



Reserpine

Table B-1 Reserpine Exact Masses

Reserpine (C33H40N2O9)

MassDescription

609.28066Molecular Ion C33H41N2O9

448.19659Fragment C23H30NO8

397.21218Fragment C23H29N2O4

365.18597Fragment C22H25N2O3

236.12812Fragment C13H18NO3

195.06519Fragment C10H11O4

174.09134Fragment C11H12NO


BExact Masses and ChemicalFormulas

Note: Not all of the symbols in the following table are applicable to every instrument.

DescriptionSymbol

Alternating current

Amperes (current)A

Authorized representative in the European community

Biohazard

CE Marking of Conformity

CSA mark. Indicates electrical safety certification for the US market.

Catalogue number

China RoHS Caution Label. The electronic information product contains certain toxic orhazardous substances. The center number is the Environmentally Friendly Use Period(EFUP) date, and indicates the number of calendar years the product can be in operation.Upon the expiration of the EFUP, the product must be immediately recycled. The circlingarrows indicate the product is recyclable. The date code on the label or product indicatesthe date of manufacture.

China RoHS logo. The device does not contain toxic and hazardous substances or elementsabove the maximum concentration values, and it is an environmentally-friendly productthat can be recycled and reused.


CGlossary of Symbols

DescriptionSymbol

Consult instructions for use.

Data Matrix symbol that can be scanned by a barcode reader to obtain a unique deviceidentifier (UDI).

Ethernet connection

Explosion Hazard

Fire Hazard

Fragile

Fuse

HertzHz

High Voltage. Electrical Shock HazardIf the main cover must be removed, contact a SCIEX representative to prevent electricshock.

Hot Surface Hazard

Ionizing Radiation Hazard

Keep dry.

Do not expose to rain.

Relative humidity must not exceed 99%.


Glossary of Symbols

DescriptionSymbol

Keep upright.

Laser Radiation Hazard

Lifting Hazard

Manufacturer

Personal Injury Hazard

Pinch Hazard

Pressurized Gas Hazard

Protective Earth (ground)

Puncture Hazard

Serial number

Toxic Chemical Hazard

USB 2.0 connection

Ultraviolet Radiation Hazard


Glossary of Symbols

DescriptionSymbol

Volt Ampere (power)VA

Volts (voltage)V

WEEE. Do not dispose of equipment as unsorted municipal waste.

WattsW

yyyy-mm-ddDate of manufacture


Glossary of Symbols

Note: If any of the labels used to identify a component become detached, contact an FSE.

Translation (if applicable)Label

FOR RESEARCH USE ONLY. NOT FOR USE INDIAGNOSTIC PROCEDURES.

FOR RESEARCH USE ONLY. NOT FOR USE INDIAGNOSTIC PROCEDURES.

IMPACT INDICATOR

SENSITIVE PRODUCT WARNING

Note: If the indicator is tripped, then this containerhas been dropped or otherwise mishandled. Make anote on the Bill of Lading and then check for damage.Any claims for shock damage require a notation.

IMPACT INDICATOR

SENSITIVE PRODUCT WARNING

IMPORTANT!RECORD ANY VISIBLE CRATE DAMAGE, INCLUDINGTRIPPED IMPACT-O-GRAPH OR TIP-N-TELL INDICATORS,ON THE WAYBILL BEFORE ACCEPTING SHIPMENT.

NOTIFY YOUR LOCAL SCIEX CUSTOMER SUPPORTENGINEER IMMEDIATELY.

IMPORTANT!

RECORD ANY VISIBLE CRATE DAMAGE, INCLUDINGTRIPPED IMPACT-O-GRAPH OR TIP-N-TELL INDICATORS,ON THE WAYBILL BEFORE ACCEPTING SHIPMENT.

NOTIFY YOUR LOCAL SCIEX CUSTOMER SUPPORTENGINEER IMMEDIATELY.

Tilt Indicator

Note: Indicates whether the container was tipped ormishandled. Write on the Bill of Lading and inspectfor damage. Any claims for tipping require a notation.

TIP & TELL

Tilt Indicator

Note: Indicates whether the container was tipped ormishandled. Write on the Bill of Lading and inspectfor damage. Any claims for tipping require a notation.

TiltWatch PLUS

ShockWatch


DGlossary of Warnings

Translation (if applicable)Label

WARNING: DO NOT OPERATE WITHOUT FIRSTENSURING BOTTLE CAP IS SECURED.

Note: This warning is attached to the source exhaustwaste bottle.

WARNING: DO NOT OPERATE WITHOUT FIRSTENSURING BOTTLE CAP IS SECURED.

X500R Systems:

WARNING: Lifting Hazard.

NINE PERSONS REQUIRED TO LIFT THIS EQUIPMENT.


NINE PERSONS REQUIRED TO LIFT THIS EQUIPMENT.

X500B Systems:


TEN PERSONS REQUIRED TO LIFT THIS EQUIPMENT.


TEN PERSONS REQUIRED TO LIFT THIS EQUIPMENT.

WARNING: NO USER SERVICEABLE PARTS INSIDE.REFER SERVICING TO QUALIFIED PERSONNEL.

Note: Consult instructions for use.

WARNING: NO USER SERVICEABLE PARTS INSIDE.REFER SERVICING TO QUALIFIED PERSONNEL.


Glossary of Warnings

sciex x500 qtof system user guide€¦ · replace the cds bottle ... import a library database...

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