Web Release Date: December 20,
Competitive Immunoassays for Simultaneous Detection of Metabolites and Proteins Using Micromosaic Patterning


and

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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