Quality evaluation of five commercial enzyme linked immunosorbent assay kits for detecting aflatoxin b1 in feedstuffs

The objective of this study was to evaluate the quality of five commercial enzyme linked immunosorbent assay (ELISA) kits (A, B, C, D, and E) from different suppliers for detecting aflatoxin B1 (AFB1). AFB1-free corn samples supplemented with different levels of AFB1 (5, 10, and 20 μg/kg) were used...

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Détails bibliographiques
Publié dans:Asian-Australasian journal of animal sciences. - 1998. - 28(2015), 5 vom: 29. Mai, Seite 691-6
Auteur principal: Sun, Dan-Dan (Auteur)
Autres auteurs: Gu, Xu, Li, Jun-Guo, Yao, Ting, Dong, Ying-Chao
Format: Article en ligne
Langue:English
Publié: 2015
Accès à la collection:Asian-Australasian journal of animal sciences
Sujets:Journal Article Aflatoxin B1 Enzyme Linked Immunosorbent Assay Kit Evaluation Feedstuffs
Description
Résumé:The objective of this study was to evaluate the quality of five commercial enzyme linked immunosorbent assay (ELISA) kits (A, B, C, D, and E) from different suppliers for detecting aflatoxin B1 (AFB1). AFB1-free corn samples supplemented with different levels of AFB1 (5, 10, and 20 μg/kg) were used as positive controls and 6 replicates of each control sample were tested to evaluate the accuracy and precision of these kits. In addition, we also evaluated the performance of these ELISA kits for AFB1 in 30 feed samples, including corn, distillers dried grains with soluble, wheat samples, soybean meal, and poultry feed, which were verified by high performance liquid chromatography. Results showed that the coefficients of variation ranged from 1.18% to 16.22% in intra-plate and 2.85% to 18.04% in inter-plate for the determination of AFB1. The half maximal inhibitory concentration for five kits ranged from 3.72 to 7.22 μg/kg. The quantitation limits of AFB1 were all under the legal limit in China but somewhat inconsistent with kit instructions. Although the recovery rate of four of the five kits were either less than 90% or more than 110%, all these values were acceptable in practice. Two kits had high false positive rates (C and E). In conclusion, our results revealed that the qualities of five tested ELISA kits were significantly different
Description:Date Completed 30.04.2015
Date Revised 01.10.2020
published: Print
Citation Status PubMed-not-MEDLINE
ISSN:1011-2367
DOI:10.5713/ajas.14.0868