LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
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<strong>LabAutomation</strong><strong>2006</strong><br />
4:30 pm Tuesday, January 24, <strong>2006</strong> Track 2: Micro- and Nanotechnologies Room: Pasadena<br />
Wyndham Palm Springs Hotel<br />
James P. Landers<br />
Co-Author(s)<br />
University of Virginia<br />
Chris Easley, James Karlinsey, Joan Bienvenue, Lindsay Legendre<br />
Charlottesville, Virginia<br />
Mike Roper, Rebecca McClure, Erik Hewlett, Molly Hughes<br />
landers@virginia.edu<br />
University of Virginia<br />
Tod J. Merkel, Mayo Clinic<br />
Jerome P. Ferrance, University of Virginia<br />
Microdevices with Integrated Sample Preparation for Ultrafast Sample-In/Answer-Out<br />
Genetic Analysis<br />
Microdevices capable of genetic analysis with sample-in/answer-out capabilities must be able to accept real-world samples, execute<br />
multiple, sequential sample preparation steps, and then provide an interpretable read-out following separation and detection. These<br />
processes involve chromatographic separation of sample components for isolation of DNA, the enzyme-mediated amplification of target<br />
DNA sequences in a temperature-dependent manner, the electrophoretic separation of the products of amplification, and detection by<br />
fluorescence. In order to accomplish the tasks within the nanospace of the microfluidic architecture, there has to be excquisite fluidic control<br />
of nanoliter volume flow. This is accomplished using a single nanoliter-flow syringe pump, a series of elastomeric valves, and resistrictive<br />
flow built into the microchannel architecture – together these allow for precise control of fluid flow through the sample preparation domains<br />
and into the separation domain. Combining these with the use of in-line diode- and capacitor-like structures, fluidic analogs of their electrical<br />
counterparts, a simplistic approach to fluidic control on microdevices begins to evolve. The application of the integrated microchip is<br />
demonstrated with three independent applications: the diagnosis of whooping cough from one microliter of human nasal wash, the detection<br />
of anthrax in 250 nanoliters of mouse blood, and finally, the diagnosis of T-cell lymphoma from a microliter of patient whole blood. Together<br />
these represent a microchip capable of sample-in/answer-out analysis - a bona fide micro-total analysis system.<br />
9:00 am Wednesday, January 25, <strong>2006</strong> Track 2: Micro- and Nanotechnologies Room: Pasadena<br />
Wyndham Palm Springs Hotel<br />
Larry Kricka<br />
University of Pennsylvania Medical Center<br />
Philadelphia, Pennsylvania<br />
kricka@mail.med.upenn.edu<br />
The Scope and Promise of Nanotechnology in Clinical Diagnostics<br />
Micro and the nano-scale miniaturization provide new avenues for improving the effectiveness and accessibility of clinical testing.<br />
Microtechnology (lab-on-a-chip) has been adapted for many types of assay procedures (e.g., CE, PCR, cell isolation) and a range of<br />
microfluidic, bioelectronic and microarray DNA and protein chips have been developed. A compelling advantage of miniaturization is<br />
integration of multiple steps in an analytical process on a single chip. Nanotechnology (0.1 nm - 100 nm) is a rapidly evolving science<br />
that has already found commercial success (e.g., nanoparticle sun screen and cosmetics). Emerging analytical applications for<br />
nanotechnology include nano-pores, tubes, -particles, -fibers and other types of nano-object (e.g., immunoassay labels based on<br />
enzyme-loaded carbon nanotubes, glucose sensors based on glucose oxidase/ferricyanide coated carbon nanotubes, nanoparticle labe<br />
for multiplexed assays, nanopores for high-throughput DNA sequencing, 3-D hydrogel nanoarrays for direct glucose sensing). In parallel,<br />
more extensive research and development in nanoelectronics promises even smaller instruments and devices. These developments taken<br />
together with all pervasive wifi, may herald a major shift in health care generally, and clinical testing in particular, in which small wifi-enabled<br />
wearable or implantable monitoring devices transmit a constant stream of information to a central server that is automatically monitored by<br />
medical staff. Developments in micro and nanotechnology provide the underlying technological foundation for such a change - however,<br />
progress in this direction will need not only the full realization of the technical promise of the emerging miniaturization technologies but also<br />
significant economic motivation and social change.<br />
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