Anal. Chem., 80 (2), 444 -450, 2008. 10.1021/ac7019046 S0003-2700(70)01904-2
Web Release Date: December 20, 2007

Copyright © 2007 American Chemical Society

Competitive Immunoassays for Simultaneous Detection of Metabolites and Proteins Using Micromosaic Patterning

Brian M. Murphy, Xinya He, David Dandy, and Charles S. Henry*

Department of Chemistry, and Department of Chemical and Biochemical Engineering, Colorado State University, Fort Collins, Colorado 80523

Received for review September 11, 2007. Accepted October 25, 2007.

Abstract:

New high-throughput immunoassay methods for rapid point-of-care diagnostic applications represent an unmet need and current focus of numerous innovative methods. We report a new micromosaic competitive immunoassay developed for the analysis of the thyroid hormone thyroxine (T4), inflammation biomarker C-reactive protein (CRP), and the oxidative damage marker 3-nitrotyrosine (BSA-3NT) on a silicon nitride substrate. To demonstrate the versatility of the method, both direct and indirect format competitive immunoassays were developed and could be applied simultaneously for single samples. Signals from standard solutions were fit to a logistic equation, allowing simultaneous detection of T4 (7.7-257.2 nM), CRP (0.3-4.2 g/mL), and BSA-3NT (0.03-22.3 g/mL). Total assay time including sample introduction, washing, and fluorescence measurement was less than 45 min. Dissociation constants for affinity pairs in the system have been estimated using regression. This proof-of-concept experiment shows that both small and macromolecular biomarkers can be quantified from a single sample using the method and suggests that groups of clinically related analytes may be analyzed by competitive micromosaic immunoassay techniques.


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