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LabAutomation 2006 - SLAS

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MP57<br />

Andre Marziali<br />

University of British Columbia<br />

Vancouver, Canada<br />

andre@physics.ubc.ca<br />

Where Laboratory Technologies Emerge and Merge<br />

Co-Author(s)<br />

David Broemeling, Joel Pel, Stephen Inglis<br />

Neha Shah, Carolyn Cowdell, Gosuke Shibahara<br />

Lorne Whitehead<br />

A Powerful New Device and Method for Isolating and Pre-Concentrating DNA for Early<br />

Detection of Cancer, Disease, and Pathogens<br />

Rapid isolation and detection of nucleic acids from exfoliated tumor cells or pathogens in human bodily fluids could lead to improvements<br />

in our capacity for early detection and identification of cancer and infectious disease. However, nucleic acid based early diagnosis is limited<br />

by the difficulty of extracting low abundance DNA from body fluids that are rich in unwanted contaminants and cellular debris. We have<br />

developed a novel instrument for isolating and pre-concentrating nucleic acids from complex samples including blood serum and bodily<br />

fluids. This instrument will serve as a front-end to existing detection technologies (e.g. PCR and microarrays) to improve their performance<br />

for detection of DNA biomarkers in human samples and thus enable cost-effective early detection of cancer and pathogens.<br />

Using a novel method of 2-D nonlinear electrophoresis capable of injecting DNA from an aqueous solution into sieving media with inherent<br />

selection parameters, we can achieve powerful separation and high concentration of DNA from contaminants without the clogging<br />

difficulties associated with filtration. This technique represents a conceptually new general method for simple, automatable, inexpensive,<br />

and selective concentration of nucleic acids directly from raw, unfiltered samples. Other applications of this technology lie in areas of<br />

biodefense to act as a front end for biomarker-based pathogen detection systems, as we have demonstrated DNA concentration factors<br />

exceeding 10,000 and factors of 106 are expected to be obtainable. This method also allows for concentration of intact high molecular<br />

weight DNA with potential applications in areas of metagenomics and drug discovery.<br />

MP58<br />

Peyman Najmabadi<br />

University of Toronto<br />

Toronto, Ontario, Canada<br />

najm@mie.utoronto.ca<br />

Co-Author(s)<br />

Andrew A. Goldenberg<br />

Andrew Emili<br />

University of Toronto<br />

New Flexible Laboratory Automation System Concepts for Biotechnology<br />

Research Laboratories<br />

Research laboratories are playing a major role in biotechnology. Scientists in these laboratories are performing diverse types of protocols<br />

and tend to continuously modify them as part of their research. At the same time, high throughput implementation of experiments is highly<br />

demanded. Therefore, flexible automation systems are required to improve the productivity of these laboratories. Most of automation<br />

systems available on the market are claimed to be flexible, but still do not address the whole spectrum of needs. This paper is a system<br />

level study of hardware flexibility of laboratory automation concepts. Flexibility was systematically modeled through the introduction of three<br />

parametric measures: Functional, Structural and Throughput. New quantitative measures for these parameters in the realm of Axiomatic<br />

Theory were proposed. The method was employed for flexibility evaluation of currently used automation concepts. Based on the result of<br />

this analysis, two new automation concepts were proposed: (i) Total Modular Laboratory Automation, a new approach to implementation<br />

of robotic-based laboratory automation systems in which robotic arms are substituted with modular arms. It was shown that this new<br />

concept improves structural and throughput flexibility of robotic-based systems; (ii) Distributed Motion Laboratory Automation, a new<br />

integration of robotic-based and track-based automation approaches. In this approach, liquid handling and transportation end-effectors<br />

are moving on transportation rails. It was shown that this concept improves functional flexibility of track-based systems. As case studies,<br />

automation of various protein purification protocols were considered through aforementioned new concepts and their improved flexibility<br />

were shown in comparison with traditional concepts.<br />

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