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LabAutomation 2006 - SLAS

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Where Laboratory Technologies Emerge and Merge<br />

3:30 pm Tuesday, January 24, <strong>2006</strong> Track 2: Micro- and Nanotechnologies Room: Pasadena<br />

Wyndham Palm Springs Hotel<br />

Paul Bohn<br />

University of Illinois<br />

Urbana, Illinois<br />

bohn@scs.uiuc.edu<br />

Nanofluidics and Mass-Limited Chemical Analysis: Nanocapillary Array Membranes as<br />

Switchable Fluidic Elements for Multidimensional Analyses<br />

Motivated by problems posed by biothreat agents, a grand challenge problem for contemporary chemical analysis is the handling and<br />

characterization of mass-limited samples. Our approach is to integrate nanometer-scale analytical unit operations into three-dimensional<br />

architectures to create integrated fluidic circuits, i.e. structures which handle fluids with the same digital control protocols used by<br />

integrated electronic circuits. We are exploring externally controllable interconnects, employing nanocapillary array membranes containing<br />

1-104 nanometer diameter-channels, to produce hybrid three-dimensional fluidic architectures, in which controllable nanofluidic transfer is<br />

achieved by controlling applied bias, polarity and density of the immobile nanopore surface charge, and the impedance of the nanopore<br />

relative to the microfluidic channels. Such multi-level microfluidic structures are analogous to the massively three-dimensional architectures<br />

characteristic of VLSI electronics and open the way for complex arrays of fluidic manipulations to be realized.<br />

4:00 pm Tuesday, January 24, <strong>2006</strong> Track 2: Micro- and Nanotechnologies Room: Pasadena<br />

Wyndham Palm Springs Hotel<br />

Stephen C. Jacobson<br />

Co-Author(s)<br />

Indiana University<br />

Zexi Zhuang<br />

Bloomington, Indiana<br />

jacobson@indiana.edu<br />

Margaret A. Lerch<br />

Multidimensional Separations of Peptides on Microfluidic Devices<br />

For many of the electrokinetically driven separation techniques demonstrated on microfluidic devices, the separative performance<br />

measured per unit length is similar to or exceeds that of conventional capillary separations. These high performance separations can also<br />

be applied to separations in multiple dimensions. In part, high performance is maintained by precise sample handling between dimensions.<br />

This can be achieved by rapid switching of the fluid streams and designing the channel architecture to effectively transition the sample<br />

from the first to the second dimension. A serial-to-parallel format is being developed where the first dimension separation is conducted in<br />

a single channel and the second dimension separation in an array of parallel channels. Also, a planar format is being considered where the<br />

first and second dimension separations are both performed in a rectangular channel with a high aspect ratio. Device design, operation, and<br />

performance will be discussed.<br />

67

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