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Development of an automated flow-based spectrophotometric immunoassay for continuous detection of zearalenone

Author(s)
Jantra, Jongjit
Zór, Kinga
Sanders, Melanie
De Saeger, Sarah
Hedström, Martin
Mattiasson, Bo
Date Issued
May 1, 2020
Type
Article
DOI
10.1002/bab.1876
Abstract
Considering the widespread contaminations of food products with mycotoxins, it is important to develop, robust, time- and cost-effective detection methods. We developed and optimized an immunoassay using a continuous flow system for the detection of zearalenone (ZEN). The assay was performed in a flow mode using an automated sequential injection system. Time for an assay cycle was 18 Min. Under optimal conditions, the limit for quantification for ZEN was 0.40 µg L−1 with a linear dependency between concentration and signal amplitude between 0.10 and 10 µg L−1. The assay proved to be robust and reliable with 13% relative standard deviation between measurements. By dissociating the antigen–antibody complex using a regeneration solution, we showed 50 times reusability of the immobilized antibodies without affecting the antigen-binding properties.
Citation
Biotechnology and Applied Biochemistry, 67(3), 375-382, 2020
Subjects

bioanalysis

flow-ELISA

immunoassay

mycotoxin

sequential injection

zearalenone

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