bme 273 senior design project group 25 “mems in the market”
DESCRIPTION
BME 273 Senior Design Project Group 25 “MEMs in the Market”. Problem. Drug companies demand a MEMs device that allows mobile, On-Chip drug testing, but at this point, that demand has not been met. Primary Objective. - PowerPoint PPT PresentationTRANSCRIPT
BME 273BME 273Senior Design ProjectSenior Design Project
Group 25Group 25“MEMs in the Market”“MEMs in the Market”
ProblemProblem
Drug companies demand a MEMs device Drug companies demand a MEMs device that allows mobile, On-Chip drug testing, that allows mobile, On-Chip drug testing, but at this point, that demand has not been but at this point, that demand has not been metmet
Primary ObjectivePrimary Objective
Our primary objective Our primary objective is to create a MEMs is to create a MEMs On-Chip dual cell On-Chip dual cell culture device at the culture device at the pico-liter volume pico-liter volume scale that allows for scale that allows for automated cell automated cell culturing and sensing culturing and sensing for the testing of for the testing of drugs and other drugs and other perfused substances.perfused substances.
GoalsGoals
Primary goal:Primary goal: Create two cell cultures, each 720 pico-liter Create two cell cultures, each 720 pico-liter
volumes, on one chip according to previous volumes, on one chip according to previous specificationsspecifications
Show that these cell cultures allow for cells to Show that these cell cultures allow for cells to retain life during experimentsretain life during experiments
Secondary goals:Secondary goals: Create On-Chip sensors that allow us to Create On-Chip sensors that allow us to
sense the metabolism/response of cells to sense the metabolism/response of cells to different stimuli (i.e., drugs)different stimuli (i.e., drugs)
Solution OriginalSolution Original
SolutionSolution
Primary Design: (picture)Primary Design: (picture)
Solution ContinuedSolution Continued
SolutionSolution
Secondary Design:Secondary Design:
SolutionSolution
Experimental Methods:Experimental Methods:
Load cells into deviceLoad cells into device
Begin perfusionBegin perfusion
Wait 24 hrs., 48 hrs., etc.Wait 24 hrs., 48 hrs., etc.
At different times periods test cell viability At different times periods test cell viability via fluorescencevia fluorescence
Test fluorescence via imagingTest fluorescence via imaging
MaterialsMaterials
Polydimethlysiloxane (PDMS)Polydimethlysiloxane (PDMS)
Negative Resist (SU-8)Negative Resist (SU-8)
Silicon WafersSilicon Wafers
MEMS laboratoryMEMS laboratory
8 mm masks8 mm masks
Platinum (working electrodes)Platinum (working electrodes)
Silver (reference Ag/AgCl electrodes)Silver (reference Ag/AgCl electrodes)
Fabrication StepsFabrication Steps
Lay down SU-8 on silicon wafer, expose using Lay down SU-8 on silicon wafer, expose using mask, and develop lower region for cell insertion mask, and develop lower region for cell insertion and perfusion.and perfusion.
Cast PDMS replica of masterCast PDMS replica of master
Lay down SU-8 on silicon wafer, expose using Lay down SU-8 on silicon wafer, expose using mask, and develop upper region for pneumatic mask, and develop upper region for pneumatic control of cell insertion channels.control of cell insertion channels.
Cast PDMS replica of master and then lay over Cast PDMS replica of master and then lay over top of lower regiontop of lower region
Business StrategyBusiness Strategy
ObjectiveObjective: Developing a strategy : Developing a strategy to market this BioMEMS device to to market this BioMEMS device to
major drug companiesmajor drug companies
Main Focus PointsMain Focus Points
Cost efficiencyCost efficiency Currently, $400-800 million and 10 years per drugCurrently, $400-800 million and 10 years per drug Lower cost due to decrease in reagent and labor Lower cost due to decrease in reagent and labor
usageusage <$1 per BioMEMS chip<$1 per BioMEMS chip
Scale up the number of cell cultures per Scale up the number of cell cultures per experimentexperiment Higher speed Higher speed faster experiments faster experiments
Greater control and modularity Greater control and modularity Portable experimentation Portable experimentation
Market BarriersMarket Barriers
Government regulation of medical devicesGovernment regulation of medical devices
Reluctance of pharmaceutical industry to Reluctance of pharmaceutical industry to universally invest lots of moneyuniversally invest lots of money
Lack of funding for BioMEMS start-up Lack of funding for BioMEMS start-up companiescompanies
Scaling up production of prototypesScaling up production of prototypes
Market PotentialMarket Potential
Worldwide MEMS market estimateWorldwide MEMS market estimate
(in billions of $)(in billions of $) 2003 3.852003 3.85 2004 4.52004 4.5 2005 5.42005 5.4 2006 6.22006 6.2 2007 72007 7
Source: Yole DevelopmentSource: Yole Development
2005 forecast MEMS markets by sector Automotive 41% Telecom 29% Bio-med 16% Military 3% Other 11%
Source: Peripheral Research Corp, Santa Barbara, Calif.
Industry ContactsIndustry Contacts
PfizerPfizerJohnson & JohnsonJohnson & JohnsonNovartisNovartisMEMS Industry GroupMEMS Industry GroupMicrochips, Inc.Microchips, Inc.ISSYS ISSYS Boehringer IngelheimBoehringer IngelheimAffymetrix, Inc.Affymetrix, Inc.Caliper Life SciencesCaliper Life SciencesCepheidCepheidOrchid CellmarkOrchid CellmarkRoger H. GraceRoger H. Grace
Author “The New MEMS and Author “The New MEMS and Their Killer Apps”Their Killer Apps”
http://finance.yahoo.com
ReferencesReferences
Fabrication of miniature Clark oxygen Fabrication of miniature Clark oxygen sensor integrated with microstructuresensor integrated with microstructure Ching-Chou Wu, Tomoyuki Yasukawa, Hitoshi Ching-Chou Wu, Tomoyuki Yasukawa, Hitoshi
Shiku, Tomokazu MatsueShiku, Tomokazu Matsue
A BioMEMS Review: MEMS Technology A BioMEMS Review: MEMS Technology for Physiologically Integrated Devicesfor Physiologically Integrated Devices AMY C. RICHARDS GRAYSON, REBECCA AMY C. RICHARDS GRAYSON, REBECCA
S. SHAWGO, AUDREY M. JOHNSON, S. SHAWGO, AUDREY M. JOHNSON, NOLAN T. FLYNN, YAWEN LI, MICHAEL J. NOLAN T. FLYNN, YAWEN LI, MICHAEL J. CIMA, AND ROBERT LANGERCIMA, AND ROBERT LANGER