Detection of analyte binding to microarrays using gold nanoparticle labels and a desktop scanner
Author(s) -
Anpan Han,
Martin Dufva,
Erik Belleville,
Claus Bo Vöge Christensen
Publication year - 2003
Publication title -
lab on a chip
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.064
H-Index - 210
eISSN - 1473-0197
pISSN - 1473-0189
DOI - 10.1039/b310814g
Subject(s) - immunoassay , colloidal gold , analyte , scanner , conjugate , chemistry , biosensor , chromatography , materials science , analytical chemistry (journal) , nanoparticle , antibody , nanotechnology , computer science , mathematics , biology , artificial intelligence , mathematical analysis , immunology
Microarray hybridization or antibody binding can be detected by many techniques, however, only a few are suitable for widespread use since many of these detection techniques rely on bulky and expensive instruments. Here, we describe the usefulness of a simple and inexpensive detection method based on gold nanoparticle labeled antibodies visualized by a commercial, office desktop flatbed scanner. Scanning electron microscopy studies showed that the signal from the flatbed scanner was proportional to the surface density of the bound antibody-gold conjugates, and that the flatbed scanner could detect six attomoles of antibody-gold conjugates. This detection system was used in a competitive immunoassay to measure the concentration of the pesticide metabolite 2,6-dichlorobenzamide (BAM) in water samples. The results showed that the gold labeled antibodies functioned comparably with a fluorescent based immunoassay for detecting BAM in water. A qualitative immunoassay based on gold-labeled antibodies could determine if a water sample contained BAM above and below 60-70 ng L(-1), which is below the maximum allowed BAM concentration for drinking water (100 ng L(-1)) according to European Union legislation.
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