Electrokinetically Driven Microfluidic Chips with Surface-Modified Chambers for Heterogeneous Immunoassays

Arash Dodge,* Karl Fluri, Elisabeth Verpoorte, and Nico F. de Rooij
Sensors, Actuators and Microsystems Laboratory, Institute of Microtechnology, University of Neuchtel, Rue Jaquet-Droz 1, CH-2007 Neuchtel, Switzerland
Anal. Chem., 2001, 73 (14), pp 3400–3409
DOI: 10.1021/ac0015366
Publication Date (Web): June 5, 2001
Copyright © 2001 American Chemical Society
*

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

,

 Present address:  MDS Pharma Services Inc., Unterdorfstrasse 23, CH-8602 Wangen, Switzerland.

Abstract

This article presents the first example of a microfluidic chip for heterogeneous bioassays using a locally immobilized biospecific layer and operated electrokinetically. The reaction chamber has picoliter dimensions and is integrated into a network of microchannels etched in glass. The high affinity of protein A (PA) for rabbit immunoglobulin G (rIgG) was exploited for chip testing, with PA being immobilized on microchannel walls and fluorescently labeled (Cy5) rIgG serving as sample. It was possible to operate the chip in an immunoaffinity chromatographic manner, using electrokinetically pumped solutions. Concentration of antibody from dilute solution onto the solid phase was demonstrated, with signal gains of 30 possible. A dose−response curve for Cy5−rIgG was obtained for concentrations down to 50 nM, for an incubation time of 200 s. The flexibility of chip layout was demonstrated for competitive immunoassay of rIgG, using both a combined sample/tracer incubation and sequential addition of these solutions. With assay times generally below 5 min for this unoptimized device, the microfluidic approach described shows great potential for many high-throughput screening applications.

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History

  • Published In Issue July 15, 2001
  • Received for review December 29, 2000. Accepted April 19, 2001.

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