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omation mbers - Society for Laboratory Automation and Screening

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4:30 pm Tuesday, February 3 Microfluidics Room A4<br />

Rajiv Bharadwaj<br />

Stan<strong>for</strong>d University<br />

Building 500, Chemical Engineering,<br />

Stan<strong>for</strong>d, Cali<strong>for</strong>nia 94305<br />

rajivb@stan<strong>for</strong>d.edu<br />

A Generalized Dispersion Theory Model <strong>for</strong> Field Amplified Sample Stacking<br />

70<br />

Co-Author(s)<br />

Juan G. Santiago<br />

We will present an analytical model <strong>for</strong> concentration enhancement using field amplified sample stacking (FASS).<br />

This transient model is based on generalized dispersion theory <strong>and</strong> accounts <strong>for</strong> convective-diffusive transport<br />

of chemical species <strong>and</strong> electromigration. We model the FASS process as a one-dimensional electromigration<br />

<strong>and</strong> dispersion of two background electrolyte ions <strong>and</strong> one sample ion across an initial concentration gradient.<br />

Regular perturbation methods are used to solve <strong>for</strong> the concentration fields. The model has been validated<br />

using experiments per<strong>for</strong>med in a microchannel system. We use an acidified poly(ethylene oxide) (PEO) coating<br />

to minimize dispersion due to EOF. Also, we use CCD-based full-field, quantitative, epi-fluorescence imaging to<br />

experimentally measure the unsteady concentration fields <strong>and</strong> validate the model.<br />

8:00 am Wednesday, February 4 Microfluidics – Separations Room A4<br />

Johan V<strong>and</strong>erhoeven<br />

Free University of Brussels<br />

Pleinlaan 2<br />

Brussels, 1050 Belgium<br />

Johan.V<strong>and</strong>erhoeven@vub.ac.be<br />

Co-Author(s)<br />

David Clicq, Kris Pappaert,<br />

Sarah Vankrunkelsven, Gino Baron,<br />

Gert Desmet<br />

On the Use of Nano-Channel Flows <strong>for</strong> the Enhancemant of Micro-Analytical Separations<br />

We will report on the use of 1D nano-channel flows <strong>for</strong> the enhancement of a wide range of different microanalytical<br />

separation techniques (liquid chromatography, DNA hybridization, protein binding kinetics measurement<br />

<strong>and</strong> the size separation <strong>and</strong> classification of particles <strong>and</strong> cells). To exploit the advantages (increased mass<br />

transfer rates <strong>and</strong> reduced solvent consumption <strong>and</strong> sample dilution) of miniaturised separation systems at their<br />

most extreme limit, we replaced the traditionally employed pressure-gradient <strong>and</strong> voltage-gradient flow driving<br />

techniques by a so-called shear-<strong>for</strong>ce driven method, enabling to establish high velocity flows through channels<br />

as thin as 50 nanometer, by simply mechanically moving the bottom part of the channel wall past the (stationary)<br />

upper part of the channel wall. With this novel flow driving principle, a wide variety of different fluid substances,<br />

ranging from small molecules, <strong>and</strong> going over proteins <strong>and</strong> large DNA coils to micron-sized particles, could be<br />

transported through silicon <strong>and</strong> fused silica etched nano-channels at velocities up to 5 cm/s. Examples of nanochannel<br />

separation applications such as ultra-rapid liquid chromatography separations of a 4-component coumarin<br />

dye mixture, enhanced DNA micro-array analysis, as well as a new separation method <strong>for</strong> the size separation of<br />

cells <strong>and</strong> nano-particles will be shown <strong>and</strong> discussed.

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