LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS LabAutomation 2006 - SLAS
TP65 Henrik Svennberg Astrazeneca R&D Molndal Molndal, Sweden henrik.svennberg@astrazeneca.com LabAutomation2006 Co-Author(s) Anna-Karin Norlén Michael Wirth Färdigh LLEX and SPEX, Two Work Tools for Control of Tecan Robots During Development of Liquid-Liquid and Solid Phase Extraction Methods Sample preparation with Liquid-Liquid Extraction and Solid Phase Extraction is most conveniently performed with the aid of liquid handling robots, in our case Tecan robots. To avoid extra automation efforts, the sample preparation method should preferably be developed with the automation equipment intended for the final method. We wanted to make the liquid handling robot available for method development work by analytical chemists without skills in script writing. Therefore the LLEX and SPEX work tools were designed. They utilise Microsoft Excel as a user interface for visualised and intuitive robot command input. Some Excel formulas and Visual Basic macros are then used to create worklists. These worklists are executed by a Gemini script to control the robot. This speech/poster will describe how the work tools are designed and the use of them will be exemplified with a sample preparation method development for Nexium. The Microsoft Excel ® user interface made it very convenient for the analytical chemist to set up the method development experiments on the Tecan robot. New methods for sample preparation were established within a few Tecan runs. TP66 Bruce Tyley PerkElmer Life Sciences Downer’s Grove, Illinois bruce.tyley@perkinelmer.com Co-Author Lois Tack Positive Sample ID and Tracking with the JANUS Robotic Liquid Handling System Many key applications, such as forensic DNA processing, compound storage and high through-put screening, require strict tracking of samples to create sample records or (as required by crime labs) accurate evidence records. During an automated procedure, a sample can be transferred among several physical locations and container types where various operations in the procedure take place. These locations, whether test tubes, microtiter plates or other labware, usually are identified by one- and two-dimensional bar codes. Faithful tracking of samples as they progress through a process can be successfully automated only if the instrument system software captures and stores all sample activities related to the run. The JANUS Automated Workstations from PerkinElmer Life and Analytical Sciences support the integration of various bar code reading devices for tubes and plates. This poster presentation will illustrate how sample data, which are tracked in the JANUS system database, can be checked and verified according to user requirements. Some examples of these activities include verifying bar coded samples against laboratory worklist files from a LIMS database, checking that labware has been placed at expected positions on the instrument deck, and checking for missing and extra samples. Data from a protocol can be extracted from the database and formatted into secure sample tracking reports. Sample tracking is compatible with all variations of JANUS platforms including both the 4-tip and 8-tip Varispan arms and the Modular Dispense Technology (MDT) using 96-tip and 384-tip heads. 184
TP67 Kathleen Tivel Pfizer Global R&D San Diego, California kathleen.tivel@pfizer.com Where Laboratory Technologies Emerge and Merge Co-Author(s) Yunwen Chiu Loanne Chung Brad De Bruler Christine Aurigemma Jeff Elleraas William Farrell Recent Developments in High-Throughput Analysis and Purification by LC/MS and SFC/MS at Pfizer La Jolla Combinatorial chemistry technologies, including parallel synthesis and high-throughput analysis techniques, allow rapid synthesis and screening of potential drugs. Pfizer’s High-Throughput Discovery facility in La Jolla produces purified small-molecule targeted libraries via a highly integrated system of instrumentation, custom software and databases. While this is our primary focus, we are often called upon to provide other analytical and preparative services to allow projects to move forward with critical compounds of interest that do not fit into the process model. Our technology includes high-throughput LC/MS, SFC/MS, UV- and MS-based preparative LC and UV-based preparative SFC. These complementary techniques enabled purification of tens of thousands of compounds at the rate of up to 2,000 per week. Purity, assessed by ELSD, UV, APCI-MS, and NMR is over 85%, with a success rate generally over 60%. A single, universal analytical method is desirable, but due to the diversity of compounds produced, multiple methods are required to produce quality compounds for screening. We present recent experiments exploring technologies to ensure realistic assessment of libraries while maximizing success of preparative HPLC and SFC and increasing throughput. These include monolithic columns for analysis and purification, nitrogen chemiluminescence detection (NCD), novel columns for SFC analysis and purification and rapid unattended method screening. TP68 Mark Truesdale Genetix New Milton, United Kingdom mark.truesdale@genetix.com Co-Author(s) Irene Bramke Chris Mann Julian F Burke The Optimisation of Semi-Solid Media for High-Throughput Screening and Picking of Mammalian Cells The ability to increase the through-put of mammalian cell screening, and shorten the discovery process, is critical to all Biopharmaceutical companies. The automated screening and selective picking of clonal cell colonies direct from media offers a solution to a bottle neck in this process. The use of semi-solid media confers positional integrity on the growing cell colonies and therefore can facilitate automated screening and picking of the colonies using criteria based upon protein secretion or morphology. We will present data on semi-solid media that allows the transition from liquid to semi-solid cell culture for a range of different cell types. 185
- 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
- Page 182 and 183: TP57 Darcy Shave Waters Corporation
- Page 184 and 185: TP61 Robert Stanaker Perkin Elmer D
- Page 188 and 189: TP69 Paige Vinson Thermo Electron C
- Page 190 and 191: TP73 Thomas Weierstall Qiagen Gmbh
- Page 192 and 193: TP77 Susan Yan Pierce Biotechnology
- Page 194 and 195: TP81 Wayne Bowen TTP LabTech Melbou
- Page 196 and 197: TP85 Evan F. Cromwell Blueshift Bio
- Page 198 and 199: TP89 Wanli Xing Tsinghua University
- Page 200 and 201: TP93 Holger Gumm Sepiatec GmbH Berl
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- Page 218 and 219: LabAutomation2006 Exhibitor List (a
- Page 220 and 221: LabAutomation2006 Exhibit Hall Janu
- Page 222 and 223: Allmotion Inc. 5501 Del Oro Ct. San
- Page 225 and 226: ASDI 601 Interchange Boulevard Newa
- Page 227 and 228: Barnstead Genevac 707 Executive Bou
- Page 229: BioMicrolab 2500 Dean Lesher Drive
- Page 232: Caliper Life Sciences, Inc. 68 Elm
TP67<br />
Kathleen Tivel<br />
Pfizer Global R&D<br />
San Diego, California<br />
kathleen.tivel@pfizer.com<br />
Where Laboratory Technologies Emerge and Merge<br />
Co-Author(s)<br />
Yunwen Chiu<br />
Loanne Chung<br />
Brad De Bruler<br />
Christine Aurigemma<br />
Jeff Elleraas<br />
William Farrell<br />
Recent Developments in High-Throughput Analysis and Purification by LC/MS and<br />
SFC/MS at Pfizer La Jolla<br />
Combinatorial chemistry technologies, including parallel synthesis and high-throughput analysis techniques, allow rapid synthesis and<br />
screening of potential drugs. Pfizer’s High-Throughput Discovery facility in La Jolla produces purified small-molecule targeted libraries via a<br />
highly integrated system of instrumentation, custom software and databases. While this is our primary focus, we are often called upon to<br />
provide other analytical and preparative services to allow projects to move forward with critical compounds of interest that do not fit into the<br />
process model.<br />
Our technology includes high-throughput LC/MS, SFC/MS, UV- and MS-based preparative LC and UV-based preparative SFC. These<br />
complementary techniques enabled purification of tens of thousands of compounds at the rate of up to 2,000 per week. Purity, assessed<br />
by ELSD, UV, APCI-MS, and NMR is over 85%, with a success rate generally over 60%.<br />
A single, universal analytical method is desirable, but due to the diversity of compounds produced, multiple methods are required to produce<br />
quality compounds for screening. We present recent experiments exploring technologies to ensure realistic assessment of libraries while<br />
maximizing success of preparative HPLC and SFC and increasing throughput. These include monolithic columns for analysis and purification,<br />
nitrogen chemiluminescence detection (NCD), novel columns for SFC analysis and purification and rapid unattended method screening.<br />
TP68<br />
Mark Truesdale<br />
Genetix<br />
New Milton, United Kingdom<br />
mark.truesdale@genetix.com<br />
Co-Author(s)<br />
Irene Bramke<br />
Chris Mann<br />
Julian F Burke<br />
The Optimisation of Semi-Solid Media for High-Throughput Screening and Picking of<br />
Mammalian Cells<br />
The ability to increase the through-put of mammalian cell screening, and shorten the discovery process, is critical to all Biopharmaceutical<br />
companies. The automated screening and selective picking of clonal cell colonies direct from media offers a solution to a bottle neck in<br />
this process. The use of semi-solid media confers positional integrity on the growing cell colonies and therefore can facilitate automated<br />
screening and picking of the colonies using criteria based upon protein secretion or morphology. We will present data on semi-solid media<br />
that allows the transition from liquid to semi-solid cell culture for a range of different cell types.<br />
185