LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
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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