nysas seminar lc-ir to characterize polymeric excipients in pharmaceutical formulations 10-27-2010
DESCRIPTION
Presentataion at New York Society for Applied Spectroscopy on Oct. 27, 2010.TRANSCRIPT
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LC-IR to Characterize Polymeric Excipients
in Pharmaceutical Formulations
Ming Zhou & Tom Kearney
Spectra Analysis Instruments, Inc.
Oct. 27, 2010
Contact: [email protected]
Tel. 508-281-6276
1
Seminar at NY Section ofSociety for Applied Spectroscopy
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OUTLINE
LC-IR Hyphenated Technology: Instrumentation
Excipient Characterization: Copovidone PVP/VAc
Excipient Degradation from HME Process:
HPMCAS, Eudragit L100-55 (PEA/MAA)
Stability Study: PEG by HPLC-IR
Summary: LC-IR Applications in Pharma Formulations
Q & A
2
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December 2009 3
2004: Founded with Substantial Commercial
Experience in FTIR, LC-MS, GC
2005 & 2006: Developed LC-IR Technology
(Patent Protected)
2008: Received R&D Magazine‟s „Top 100‟ Product Award.
2009: Received Massachusetts Life Science Center‟s Award & Certification.
2007-2009: Sales to „Top Tier‟ Customers: Forensics, National Labs, Polymers
2009-Present: Explosive Activities for Pharmaceutical Excipients
The Company
257 Simarano Drive
Marlborough, MA 01752
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Scientific Excellence
4
Sid Bourne, PhD
Co-founder
Chief Scientist
Developed the first GC-IR product
while at the Argonne National
Laboratory.
Developed the “Tracer” at Bio-Rad.
Founded Bourne Scientific, Inc and
the “Detective”.
University of Minnesota, PhD.
Organic Chemistry.
William W. Carson, PE
Co-founder
V P Engineering
Over $1b revenue generated by
products covered by his 19 US patents
and 75 corresponding patents.
Registered Professional Engineer.
Former Assistant professor at Cornell
University.
Massachusetts Institute of Technology,
MS Mechanical Engineering.
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Hyphenated Technologies &
Major Applications
Liquid Chromatography
Mass
SpectroscopyInfra Red
Spectroscopy
Separation
Applications Small Molecules, Proteins Polymers
Detection &
Data Analysis
LC-MS LC-IR
Pharma API‟s Polymeric Excipients
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6
LC-IR Hyphenated System
Dell Desktop ComputerThermo-GRAMS /32 Software Package
•Library Search & Creation
•Ratio Chromatograms
•CFR 21-Part 11 Compliant
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DiscovIR Users
Merck Pharma
Johnson & Johnson Pharma
Shire Pharmaceuticals Pharma
Novartis Pharma
Du Pont Polymers
Dow Chemical Polymers
Lawrence Livermore National Lab Trace Analysis
Oak Ridge National Laboratory Environmental
Naval Research Laboratory Organics
US Army Aberdeen Proving Ground Forensics
Pennsylvania State Police Forensics
Alabama Department of Forensics Forensics
Vermont State Police Forensic lab Forensics
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Direct Deposition FTIR
& Data Processing (GPC-IR)
ZnSe Disk
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How is the Solvent Removed?
Cyclone
EvaporatorThermal Nebulization
From LC
N2 Addition
Chilled
Condenser
Waste Solvent
Particle Stream to DiscovIR
Air Cooled
Condenser
Cyclone
Evaporator
Patent pending: PCT/US2007/025207
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ZnSe Sample Disk
Auto sampler compatible
Unattended overnight runs
The ZnSe sample disk (yellow) is under vacuum without moisture or CO2 interference
Re-usable after solvent cleaning
Transmission IR analysis is done on the solid deposit.
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What is Direct Deposition FTIR?
Continuous Polymer Tracks (GPC-IR)Separated Dots from HPLC-IRSeparated Dot Depositing on Disk
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Features of DiscovIR-LC
High Quality Solid Phase Transmission IR Spectra
Real-Time On-line Detection
Microgram Sensitivity
Compatible with all LC Solvents and Gradients
• e.g. Water, ACN, Methanol, THF, Chloroform, HFIP
Compatible with all GPC/SEC Solvents
Fully Automated Operation: No Fractionation
Multi-Sample Processing: 10 Hr ZnSe Disk Time
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OUTLINE
LC-IR Hyphenated Technology: Instrumentation
Excipient Characterization: Copovidone PVP/VAc
Excipient Degradation from HME Process:
HPMCAS, Eudragit L100-55 (PEA/MAA)
Stability Study: PEG by HPLC-IR
Summary: LC-IR Applications in Pharma Formulations
Q & A
16
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Compositional Drift Analysis of
Copolymer Poly(A-B) by GPC-IR
Ratio 10/8 12/12 2/4 Total 24/24
A% 56% 50% 33% 50%
High MW Low MW Molar Mass
Ab
so
rpti
on
A/B RatioA
B
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Compositional Heterogeneity of
Copolymer Poly(A-B)
High MW Low MW Molar Mass
Ab
so
rpti
on
Ratio 10/8 12/12 2/4 Total 24/24
A% 56% 50% 33% 50%
GPC-IR
Regular FTIR Bulk 50% (NMR)
GPC
(MS)
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IR Spectrum of Copovidone
Excipient - VP/VAc Copolymer
Peak 1680 cm-1 from VP comonomer
Peak 1740 cm-1 from VAc comonomer
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GPC-IR Chromatogram Overlay with Comonomer IR Peak Ratios
Excipient Compositional Drift
w/ MWD Vs. Bulk Average
Abs. Peak Ratio: AVA / AVP = (k1*b*MVA) / (k2*b*MVP) = k (MVA / MVP) ~ Comonomer Ratio
(Molecular Weight Distribution)
Bulk Average
Copovidone
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0
.1
.2
.3
.4
.5
.6
106 104 103 102105
ma
x. IR
ab
so
rba
nce
Molecular Weight
Copovidone: sample A
30
35
40
45
50
molecular weight
distribution
% a
ceta
te c
om
onom
er
comonomer composition
distribution
Excipient Compositional Drift
w/ MWD Vs. Bulk Average
Bulk Average
40% VAc
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0
.1
.2
.3
.4
.5
.6
106 104 103 102105Molecular Weight
Copovidone: sample A
sample B
sample C
Copovidone MW Distributions from
Different Suppliers (Manf. Processes)
ma
x. IR
ab
so
rba
nce
Copovidone A gave clear tablets while Copovidone C led to cloudy ones.
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0
.1
.2
.3
.4
.5
.6
106 104 103 102105Molecular Weight
Copovidone: sample A
30
35
40
45
50
% a
ceta
te c
om
onom
er
Comonomer Composition
Distribution
sample B
sample C
0
.1
.2
.3
.4
.5
.6
106 104 103 102105
sample B
sample C
Bulk 40% VAc
ma
x. IR
ab
so
rba
nce Molecular Weight
Distribution
Copovidone Compositional Drifts
from Different Manf. Processes
Copovidone A gave clear tablets while Copovidone C led to cloudy ones.
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Excipient Characterization
by LC-IR
24
Copolymer Compositional Analysis with MW Distributions
• Comonomer Ratio Drift (Functional Groups) vs. Bulk Average
• Excipient Lot-to-Lot Variations: QbD Studies
Excipient Performance & Functional Group Correlations
• Hydrophobic/Hydrophilic Ratio Drift vs. Phase Separations
• Effects on Excipient Dissolution Behavior
Reference
(1) Chemical Heterogeneity on Dissolution of HPMC,
EU J. of Pharma Sci., P392 (2009), A. Viriden et al.
(2) Comp Drift Effect on Dissolution of PMMA/MAA,
Materials Letters, P1144 (2009), E. Manias et al.
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HPMCAS Grade-to-Grade
Difference (LF/MF/HF) by GPC-IR
M
OCH3
2830
C/HP
OH
3470
HP
CH3
1372
A
Acetyl
1235
AS
C=O
1740
HOOC-CH2-CH2-C=O
CH3-C=O
-C-O-C-
1060
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IR Band Identifications of HPMCAS
Excipients for Ratio Drift Analysis
CH3
HP
o
HOOC-CH2-CH2-C=O
O
CH3-C=O
CH3-C=O
O
CH3
O
S
A
A
MM M
M
M
M M
Groups HP M C A AS Notes
CH3 1372 HP
OCH3 2830 M
OH 3470 (Unsub. OH & HP OH) OH
COCH3 1235 A
Total C=O 1740 AS
CH2 2935 2935 2935 2935 CH2
C-O-C 1060 BackBone
(BB)
C
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HPMCAS Grade-to-Grade
Difference (HF/MF/LF) by GPC-IR
Acetyl / C=O (total AS)
HF—0.8
MF—0.5
LF—0.4
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Acetyl/TotalEster Ratio Drifts of 4 MF
Lots Compared to LF & HF HPMCAS
-- LF ---------
-- HF ---------
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OUTLINE
LC-IR Hyphenated Technology: Instrumentation
Excipient Characterization: Copovidone PVP/VAc
Excipient Degradation from HME Process:
HPMCAS, Eudragit L100-55 (PEA/MAA)
Stability Study: PEG by HPLC-IR
Summary: LC-IR Applications in Pharma Formulations
Q & A
29
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30
Excipient Degradation from
Hot Melt Extrusion Process
Hot Melt Extrusion Process: To Make Solid Dispersions
for Low Solubility Drugs to Improve Bioavailability
Degradation Issues
• Excipient & API Degradation at High Temp. (100-200C)
• Discoloration / Residues
• Degradant / API Interactions
Process Variables
• Temperature
• Time (Screw Speed)
• Torque
• Screw / Die Designs
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Excipient HPMCAS Degradation
in Hot Melt Extrusion Process
Unprocessed
Processed at 160C
Processed at 220C
Degradant
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Degradant from HPMCAS (220C)
in Hot Melt Extrusion Process
IR Database Search Result: Succinic Acid
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HPMCAS Degradation
in Hot Melt Extrusion Process
Functional Group Ratio Changes from High Temp Process (Sample C)
OH
-C=O
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GPC-IR Analysis of HPMCAS
Degradation in HME Process
Fig. A Schematic Structure of HPMC-AS
Detected Degradants: Succinic Acid & Derivatives
Detected Functionality Ratio Change: Hydroxyl Vs. Carbonyl
Help Understand Excipient Degradation Mechanism
Study Excipient / API Interactions
Define Safe Process Window: QbD
Excipient Blends with Plasticizers and Additives
CH3-C=O
HOOC-CH2-CH2-C=O
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Eudragit L100-55 Samples
from Hot Melt Extrusion Process
35
Sample # Extrusion
Temp.
Screw
Speed
Sample
Color
Sample
in THF
(~0.5%)
Degradant
Formed
?
Polymer
Changed
?
S0 Not
Processed
White Clear
Solution
S1 130 C 250 rpm Off
White
Clear
Solution
S2 160 C 250 rpm Off
White
Clear
Solution
S3 190 C 250 rpm Brownish Some
Residue
? ?
Note: Samples S1-S3 contain 20% plasticizer to assist extrusion process.
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GPC-IR Operating Conditions
& Sample Preparation
GPC Chromatograph: Agilent® 1200
• GPC Column Temperature: Ambient
• Solvent: THF at 1.0 ml/min
• Column: Jordi Gel DVB Mixed Bed– 250 x 10 mm
• Sample Injections: 100 ml at ~0.5% weight / volume THF
IR Detection
• DiscovIR-LC® solvent-removing direct-deposition solid phase FTIR
• Cyclone Temperature: 150oC
• ZnSe Disk Temperature: -10 ~ -15oC
Sample Preparation:
• 0.050 g excipient solid samples were dissolved in 10 ml THF in ~1
hr and filtered with 0.45 mm PTFE syringe filter before GPC injection
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Eudragit L100-55 Characterization by GPC-IR (Chromatograph + IR Spectra)
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Eudragit L100-55 Compositional Drift at
Different Elution Times (Red 8‟ & Blue 10‟)
COOH
1705
COOEt
1735
CH2 CH3
Areas: L R
Acid / Ester Co-Monomer Ratio ~ Acid / Ester Peak Area Ratio = [(L+R)-2L] / (2L)
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IR Spectra of L100-55 Samples atPolymer Peak Center (Elution Time ~9.4‟)
39
S0 – Green Ref
S1 – Pink 130C
S2 – Blue 160C
S3 – Black 190C
COOEt
1735
COOH
1705
CO-OH
NCE?
1805 cm-1
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Excipient L100-55 Crosslinked from
COOH to Anhydride at Higher Temp
40
COOEt
1735
COOH
1705
S0 – Green Ref
S1 – Pink 130C
S2 – Blue 160C
S3 – Black 190C
NCE?
1805 cm-1
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Summary: Eudragit L100-55
Degradation & Stability from HME
41
Sample # Extrusion
Temp.
Screw
Speed
Sample
Color
Sample
in THF
(~0.5%)
Degradant
Formed
Polymer
Change
S0 Not
Processed
White Clear
Solution
None None
S1 130 C 250 rpm Off
White
Clear
Solution
Trace
Anhydrides
S2 160 C 250 rpm Off
White
Clear
Solution
Anhydrides Acid/Ester
Ratio
Decreased
S3 190 C 250 rpm Brownish Some
Residue
Anhydrides Acid/Ester
Ratio
Decreased
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Excipient Degradation Analysis
in HME Process by GPC-IR
42
Detect Degradation Intermediates with MW Distributions
Detect Functionality Changes
Probe Polymer Degradation Mechanism
Solve Degradation Problems
Define Safe Process Window: QbD
Understand Excipient / API Interactions
HME Process Monitoring: PAT
Various Polymeric Excipients
Excipient Blends with Plasticizers and Additives
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OUTLINE
LC-IR Hyphenated Technology: Instrumentation
Excipient Characterization: Copovidone PVP/VAc
Excipient Degradation from HME Process:
HPMCAS, Eudragit L100-55 (PEA/MAA)
Stability Study: PEG by HPLC-IR
Summary: LC-IR Applications in Pharma Formulations
Q & A
43
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Forced Degradation Study of PEG Excipient by HPLC-IR
Reverse-Phase HPLC-IR with H2O/ACN; PEG-1000 before Degradation
AU Scale for all traces
1116 cm-1 band chromatogram
1607 cm-1 band chromatogram
Blue Trace: No Carboxylates
1719 cm-1 band chromatogram
Red Trace: No Aldehydes
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Degradation Intermediates Detected by
HPLC-IR from Degraded PEG
Three Chromatographic displays generated from one time ordered set of FTIR Spectra
PEG-1000 Sample Air Bubbled Overnight at 55C
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IR Identification of Degraded Intermediates
(Aldehydes & Carboxylates)
11.45 minutes
4.93 minutes
1.50 minutes
Na+ or K+ Cation
Carboxylate Salt
1607
Aldehyde
1719
Typical IR Spectra of PEG in Black
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Proposed Mechanism of PEG Oxidation
Supported by HPLC-IR Data
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OUTLINE
LC-IR Hyphenated Technology: Instrumentation
Excipient Characterization: Copovidone PVP/VAc
Excipient Degradation from HME Process:
HPMCAS, Eudragit L100-55 (PEA/MAA)
Stability Study: PEG by HPLC-IR
Summary: LC-IR Applications in Pharma Formulations
Q & A
48
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Common Polymeric Excipients
49
Cellulose Derivatives
• HydroxyPropyl Methoxy Cellulose (Hypromellose): HPMC
• HPMC Acetate Succinate: HPMC-AS
• HPMC Phthalate: HPMC-P
•HydroxyPropyl Cellulose: HPC
Copovidone: PolyVinyl Pyrrolidone / Vinyl Acetate – PVP/VAc
SoluPlus Terpolymer: PEG / PVAc / PVCap
Methacrylic or Methacrylate Copolymers: Eudragit
Polyethylene Oxide: PEO (MW > 20K) or PEG (MW < 20K), PEG/PPG
PLGA Copolymers:Biodegadable
Excipient Combinations with Plasticizers and Additives
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LC-IR Applications for Excipient
Analysis in Drug Formulations
Excipient
Manufacturing
• Process Control
• Lot-to-lot Variations
• CoA
• Novel Excipient R&D
• Trouble Shooting
Formulation Develop. Drug Manufacturing
• Incoming QC
• Excipient Functionality
• Formulation Development
• QbD
• Process Degradation (Hot Melt Extrusion)
• Define Safe Process Window / QbD
• Process Monitoring
• Trouble Shooting
Formulated Drugs
Shelf Life Stability
• Stressed Degradation
• De-Formulate Excipient Blends
• Trouble-Shoot Problem Drugs in the Market
Users: Excipient Pharma Co. Pharma Co.
Manufacturers HME Service Providers Generic Drug Co.
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Excipient QbD Space
GPC-IR-Performance
Slide from USP International Excipient Workshop (July 2009)
GPC
IR
Performance
GPC-IR
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Excipient Analysis with LC-IR
in Pharmaceutical Formulations
Polymeric Excipient Characterization
Compositional Variations with MWD: Functional Group Ratios
Lot-to-Lot, Supplier-to-Supplier Variations
Degradation Analysis in Thermal Process (HME)
Detect Degradants (Low MW)
Polymer Structural Changes:
• Cross-Linking (New Chemical Entity)
• Functional Group Changes