Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10429424 | Biosensors and Bioelectronics | 2011 | 5 Pages |
Abstract
A direct, label-free immunosensor was designed for the rapid detection and quantification of staphylococcal enterotoxin A (SEA) in buffered solutions using quartz crystal microbalance with dissipation (QCM-D) as transduction method. The sensing layer including the anti-SEA antibody was constructed by chemisorption of a self-assembled monolayer of cysteamine on the gold electrodes placed over the quartz crystal sensor followed by activation of the surface amino groups with the rigid homobifunctional cross-linker 1,4-phenylene diisothiocyanate (PDITC) and covalent linking of binding protein (protein A or protein G). Four anti-SEA antibodies (two of which from commercial source) have been selected to set up the most sensitive detection device. With the optimized sensing layer, a standard curve for the direct assay of SEA was established from QCM-D responses within a working range of 50-1000 or 2000 ng mlâ1 with a detection limit of 20 ng mlâ1. The total time for analysis was 15 min. Using a sandwich type assay, the response was ca. twice higher and consequently the lowest measurable concentration dropped down to 7 ng mlâ1 for a total assay time of 25 min.
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Physical Sciences and Engineering
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Authors
Michèle Salmain, Mahsa Ghasemi, Souhir Boujday, Jolanda Spadavecchia, Clarisse Técher, Florence Val, Vincent Le Moigne, Michel Gautier, Romain Briandet, Claire-Marie Pradier,