Microchip-Based Capillary Electrophoresis for Immunoassays:  Analysis of Monoclonal Antibodies and Theophylline

Nghia Chiem and D. Jed Harrison*
Department of Chemistry, University of Alberta, Edmonton, Alberta, T6G 2G2, Canada
Anal. Chem., 1997, 69 (3), pp 373–378
DOI: 10.1021/ac9606620
Publication Date (Web): February 1, 1997
Copyright © 1997 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.

Abstract

A microchip capillary electrophoresis device has been used to separate the reaction products of homogeneous, immunological reactions within 40 s. Determination of monoclonal mouse IgG in mouse ascites fluid, via a direct assay, and the drug theophylline in serum samples, via a competitive assay, was demonstrated on-chip. The mouse anti-bovine serum albumin IgG assay gave a linear calibration curve up to at least 135 μg/mL, with ±3% precision. The theophylline assay gave a threshold for detection of 1.25 ng/mL in diluted serum. A calibration curve of signal vs undiluted log[theophylline] is linear from 2.5 to 40 μg/mL, which includes the therapeutically useful range. Theophylline recoveries in spiked samples were 100%, within an experimental error of ±5%. A buffer system consisting of 0.05 M tricine adjusted to pH 8.0, 0.01% (w/v) Tween 20, and 40 mM NaCl was used. This buffer allowed for adequate separation (40 000 plates for theophylline; 1000 plates for theophylline−antibody complex and for human IgG) and gave reproducibility of migration times of 1−1.5% over 4-day periods, indicating minimal problems from adsorption in the uncoated chips.

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History

  • Published In Issue February 01, 1997
  • Received for review July 8, 1996. Accepted November 4, 1996.

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