LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS LabAutomation 2006 - SLAS
MP59 Irena Nikcevic University of Cincinnati Cincinnati, Ohio nikcevi@email.uc.edu LabAutomation2006 Co-Author(s) Se Hwan Lee Aigars Piruska Chong H. Ahn Patrick A. Limbach William R. Heineman Carl J. Seliskar University of Cincinnati Characterization of Cyclic Olefin Copolymer (COC) and Poly(methylmethacrylate) (PMMA) Microchips for Capillary Electrophoresis A high-throughput plastic microchip analytical technology based on capillary electrophoresis (CE) for rapid analysis and manipulation of biological samples and small molecule therapeutics important for medical and pharmaceutical research is being developed. Using plastics for fabrication material reduces the cost and eventually will lead to high-speed, mass production of disposable chips. Compared to glass (the standard material) plastic materials have different properties and thus it is important to characterize their properties before real biological assays can be performed. When designing a chip in a plastic substrate several issues must be addressed, including the materials and their properties, the scale of the system, methods of fabrication, detection scheme, and most importantly, stability and evaluation of analytical performance. The performance characteristics of single lane plastic CE separations were evaluated using mixtures of the dyes fluorescein and fluorescein isothiocyanate as model compounds. Fabrication properties, quality of fabricated chip, separation reproducibility, determination of electroosmotic flow (EOF) and electrophoretic mobility of hot embossed poly(methylmethacrylate) (PMMA), injection molded PMMA and cyclic olefin copolymer (COC) were compared with results obtained for glass chips. MP60 Aigars Piruska University of Cincinnati Cincinnati, Ohio piruska@email.uc.edu Co-Author(s) Irena Nikcevic Patrick A. Limbach William R. Heineman Carl J. Seliskar University of Cincinnati Optical Detection System for Multi-Lane Plastic Microchips High throughput analysis of disease targets and candidate pharmaceuticals are critical for new pharmaceutical discovery and to reveal insight into disease development. Our research group is developing methodology for high speed assays. Analysis is based on microchip capillary electrophoresis performed on multi lane disposable plastic chips. A method for simultaneous optical detection of all multi lane channels is demonstrated. All separation channels on the multi lane microchip are simultaneously excited by a linearly expanded laser beam and fluorescence from the analyte is detected by a CCD camera. The detailed characterization of the developed detection scheme was performed. Uniform and efficient excitation over fairly large distances (few millimeters) was achieved by using a Powel lens for laser beam expansion. The signal from adjacent channels did not show significant crosstalk. The separation performance of a model system is compared for a standard single lane and a multi lane detection system. 132
MP61 Shalini Prasad Portland State University Portland, Oregon prasads@ecs.pdx.edu Where Laboratory Technologies Emerge and Merge Co-Author(s) SudhaPrasanna Kumar, Padigi, Portland State University Tunable Nano Plasmons Based Micro cavity Bio-Chemical Sensors Micro cavity based high quality factor (Q) technology has been employed in telecommunications and data transfer for rapid, high bandwidth information exchange. The fundamental micro cavity technology has been modified and integrated with nano plasmonics and applied towards the development of highly sensitive, broad spectrum bio-chemical sensors for label free detection. The high Q technology allows for rapid detection of the chemical analytes from an air and water based environment. The micro cavities are selectively studded with metallic nanoparticles that are made sensitive to specific agents in the atmosphere. The nano structured surfaces offer dual capabilities. The first: larger surface area to facilitate better interaction, the second: amplification of the detected signal by surface plasmonics. The nanoparticle surface functionalized micro cavities are excited by an input coherent light source. This is coupled in to each cavity through optical fibers by evanescent coupling. The interaction of the chemical agent with the micro cavity surface results in a binding event similar to antibody-antigen binding. This in turn results in the modification of the intensity and/or wavelength of the input coupled light. The modified light is coupled out and analyzed to yield unique spectral identifiers associated with specific chemical agents. These sensors demonstrate very low threshold sensitivity in the order of parts per billion for a wide range of agents including but not limited to ammonia, nitrous oxide to hydrocarbons such as propane and butane. MP62 Giovanna Prout Aurora Discovery, Inc. San Diego, California giovanna_prout@auroradiscovery.com Tackling the Challenges of Cell-Based Assays in High-Throughput and High-Content Screening High-throughput screening (HTS) and the more recent technology of High-content screening (HCS) rely on the ability to screen compounds using cell-based assays. Using live cells can more effectively evaluate a drugs toxicity, potency and overall efficiency, in addition to looking at other specific cellular responses. Yet, despite the progression towards high-throughput and high-content screening, many cell-based assays are still performed in 96-well and 384-well microplates. The current dispensing instrumentation does not address the specific needs of cell-based assays and is a limiting factor in the progression toward high-throughput and high-content screening. Challenges that arise with the current dispensing instrumentation are the ability to rapidly and reliably deliver sensitive cell lines to high-density microplates through reduction of cell shearing, reducing bubble effects due to high protein media and smaller well sizes, decreasing the amount of system dead volume to conserve reagent costs, and limiting the evaporation effects due to long incubation times. Aurora Discovery’s BioRAPTR Flying Reagent Dispenser (BioRAPTR FRD) offers a novel solution for precision dispensing of cells into 384-well, 1536-well, and 3456-well microplates using efficient, non-contact micro-solenoid valve dispensing starting at 100nL volumes. Aurora Discovery’s BioRAPTR (BioRAPTR) combined with Aurora Discovery’s ChemLib Microplate technology addresses the challenges of cell-based assays and is a reliable and effective solution for miniaturization for high-throughput and high-content screening. 133
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- Page 106 and 107: MP03 Ismail Al-Abdulmohsen Saudi Ar
- Page 108 and 109: MP07 Varouj Amirkhanian eGene, Inc.
- Page 110 and 111: MP11 Sibani Biswal University of Be
- Page 112 and 113: MP15 Josh Eckman University of Utah
- Page 114 and 115: MP19 Ismet Celebi National Institut
- Page 116 and 117: MP23 Robin Clark deCODE Biostructur
- Page 118 and 119: MP27 J. Colin Cox Duke University M
- Page 120 and 121: MP31 Frank Doffing IMM - Institut f
- Page 122 and 123: MP35 Aoife Gallagher Deerac Fluidic
- Page 124 and 125: MP39 Yunseok Heo University of Mich
- Page 126 and 127: MP43 David Humphries Lawrence Berke
- Page 128 and 129: MP47 Joohoon Kim University of Texa
- Page 130 and 131: MP51 Michelle Li Saint Louis Univer
- Page 132 and 133: MP55 Philip Manning Procter & Gambl
- Page 136 and 137: MP63 Qiaosheng Pu Virginia Commonwe
- Page 138 and 139: MP67 Alexander Roth National Instit
- Page 140 and 141: MP71 Sang Jun Son University of Mar
- Page 142 and 143: MP75 Lois Tack PerkinElmer Life & A
- Page 144 and 145: MP79 Angelo Trivelli J Craig Venter
- Page 146 and 147: MP83 Tracy Worzella Promega Corpora
- Page 148 and 149: MP87 Peter Greenhalgh Astech Projec
- Page 150 and 151: MP91 David Ferrick Seahorse Bioscie
- Page 152 and 153: MP95 Christine Brideau Merck Frosst
- Page 154 and 155: TP01 Marc Pfeifer Roche Molecular S
- Page 156 and 157: TP05 Marcy Engelstein Millipore Cor
- Page 158 and 159: TP09 Aoife Gallagher Deerac Fluidic
- Page 160 and 161: TP13 Ulrike Honisch Greiner Bio-One
- Page 162 and 163: TP17 Michael Gary Jackson Beckman-C
- Page 164 and 165: TP21 Libby Kellard Millipore Danver
- Page 166 and 167: TP25 Joseph Kofman Pfizer San Diego
- Page 168 and 169: TP29 Hanh Le PerkinElmer Life and A
- Page 170 and 171: TP33 Stephen Lowry Thermo Electron
- Page 172 and 173: TP37 Donald J. Nagy California Comp
- Page 174 and 175: TP41 Clifford Olson Zinsser Analyti
- Page 176 and 177: TP45 Nick Price Invitrogen Corporat
- Page 178 and 179: TP49 Michael Raimo Arqule Inc. Wobu
- Page 180 and 181: TP53 Jim Schools Biosero, Inc Monro
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MP61<br />
Shalini Prasad<br />
Portland State University<br />
Portland, Oregon<br />
prasads@ecs.pdx.edu<br />
Where Laboratory Technologies Emerge and Merge<br />
Co-Author(s)<br />
SudhaPrasanna Kumar, Padigi,<br />
Portland State University<br />
Tunable Nano Plasmons Based Micro cavity Bio-Chemical Sensors<br />
Micro cavity based high quality factor (Q) technology has been employed in telecommunications and data transfer for rapid, high bandwidth<br />
information exchange. The fundamental micro cavity technology has been modified and integrated with nano plasmonics and applied<br />
towards the development of highly sensitive, broad spectrum bio-chemical sensors for label free detection. The high Q technology allows<br />
for rapid detection of the chemical analytes from an air and water based environment. The micro cavities are selectively studded with<br />
metallic nanoparticles that are made sensitive to specific agents in the atmosphere. The nano structured surfaces offer dual capabilities.<br />
The first: larger surface area to facilitate better interaction, the second: amplification of the detected signal by surface plasmonics. The<br />
nanoparticle surface functionalized micro cavities are excited by an input coherent light source. This is coupled in to each cavity through<br />
optical fibers by evanescent coupling. The interaction of the chemical agent with the micro cavity surface results in a binding event similar<br />
to antibody-antigen binding. This in turn results in the modification of the intensity and/or wavelength of the input coupled light. The<br />
modified light is coupled out and analyzed to yield unique spectral identifiers associated with specific chemical agents. These sensors<br />
demonstrate very low threshold sensitivity in the order of parts per billion for a wide range of agents including but not limited to ammonia,<br />
nitrous oxide to hydrocarbons such as propane and butane.<br />
MP62<br />
Giovanna Prout<br />
Aurora Discovery, Inc.<br />
San Diego, California<br />
giovanna_prout@auroradiscovery.com<br />
Tackling the Challenges of Cell-Based Assays in High-Throughput and High-Content<br />
Screening<br />
High-throughput screening (HTS) and the more recent technology of High-content screening (HCS) rely on the ability to screen compounds<br />
using cell-based assays. Using live cells can more effectively evaluate a drugs toxicity, potency and overall efficiency, in addition to looking<br />
at other specific cellular responses. Yet, despite the progression towards high-throughput and high-content screening, many cell-based<br />
assays are still performed in 96-well and 384-well microplates. The current dispensing instrumentation does not address the specific<br />
needs of cell-based assays and is a limiting factor in the progression toward high-throughput and high-content screening. Challenges that<br />
arise with the current dispensing instrumentation are the ability to rapidly and reliably deliver sensitive cell lines to high-density microplates<br />
through reduction of cell shearing, reducing bubble effects due to high protein media and smaller well sizes, decreasing the amount of<br />
system dead volume to conserve reagent costs, and limiting the evaporation effects due to long incubation times. Aurora Discovery’s<br />
BioRAPTR Flying Reagent Dispenser (BioRAPTR FRD) offers a novel solution for precision dispensing of cells into 384-well, 1536-well,<br />
and 3456-well microplates using efficient, non-contact micro-solenoid valve dispensing starting at 100nL volumes. Aurora Discovery’s<br />
BioRAPTR (BioRAPTR) combined with Aurora Discovery’s ChemLib Microplate technology addresses the challenges of cell-based assays<br />
and is a reliable and effective solution for miniaturization for high-throughput and high-content screening.<br />
133