Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk

The flunixin residues in foods of animal origin could pose hazards for human health. In this paper, a broad-selectivity polyclonal antibody was obtained using 5-hydroxyflunixin coupled with bovine serum albumin as the immunogen. The semi-inhibitory concentration (IC50) of the polyclonal antibody was...

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Main Authors: Xiaona Chen, Shimin Peng, Chen Liu, Xin Zou, Yuebin Ke, Wenxiao Jiang
Format: Article
Language:English
Published: Taylor & Francis Group 2019-01-01
Series:Food and Agricultural Immunology
Subjects:
Online Access:http://dx.doi.org/10.1080/09540105.2019.1577365
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spelling doaj-9f1a660a2929498c8c47a0ba85e6c0352020-11-25T01:46:30ZengTaylor & Francis GroupFood and Agricultural Immunology0954-01051465-34432019-01-0130132033210.1080/09540105.2019.15773651577365Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milkXiaona Chen0Shimin Peng1Chen Liu2Xin Zou3Yuebin Ke4Wenxiao Jiang5Shenzhen University Health Sciences CenterShenzhen University Health Sciences CenterShenzhen People’s HospitalShenzhen University Health Sciences CenterShenzhen Center for Disease Control and PreventionShenzhen University Health Sciences CenterThe flunixin residues in foods of animal origin could pose hazards for human health. In this paper, a broad-selectivity polyclonal antibody was obtained using 5-hydroxyflunixin coupled with bovine serum albumin as the immunogen. The semi-inhibitory concentration (IC50) of the polyclonal antibody was 1.43 ng/mL for flunixin and 0.29 ng/mL for 5-hydroxyflunixin, respectively, which were far below the maximum residue limits set by the United States, the European Union and China. The limits of detection were calculated to be 2.98 μg/kg for flunixin in bovine muscle and 0.78 μg/L for 5-hydroxyflunixin in milk. In spike and recovery tests, the average recovery ranged from 83% to 105%, with a satisfying coefficient of variance ranging from 5.8% to 11.3%. Furthermore, the ELISA method was validated by a well-established LC-MS/MS method. These results proved that the established method is suitable for flunixin and 5-hydroxyflunixin residue analysis.http://dx.doi.org/10.1080/09540105.2019.1577365flunixin5-hydroxyflunixinimmunoassaybovine musclemilk
collection DOAJ
language English
format Article
sources DOAJ
author Xiaona Chen
Shimin Peng
Chen Liu
Xin Zou
Yuebin Ke
Wenxiao Jiang
spellingShingle Xiaona Chen
Shimin Peng
Chen Liu
Xin Zou
Yuebin Ke
Wenxiao Jiang
Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
Food and Agricultural Immunology
flunixin
5-hydroxyflunixin
immunoassay
bovine muscle
milk
author_facet Xiaona Chen
Shimin Peng
Chen Liu
Xin Zou
Yuebin Ke
Wenxiao Jiang
author_sort Xiaona Chen
title Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
title_short Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
title_full Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
title_fullStr Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
title_full_unstemmed Development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
title_sort development of an indirect competitive enzyme-linked immunosorbent assay for detecting flunixin and 5-hydroxyflunixin residues in bovine muscle and milk
publisher Taylor & Francis Group
series Food and Agricultural Immunology
issn 0954-0105
1465-3443
publishDate 2019-01-01
description The flunixin residues in foods of animal origin could pose hazards for human health. In this paper, a broad-selectivity polyclonal antibody was obtained using 5-hydroxyflunixin coupled with bovine serum albumin as the immunogen. The semi-inhibitory concentration (IC50) of the polyclonal antibody was 1.43 ng/mL for flunixin and 0.29 ng/mL for 5-hydroxyflunixin, respectively, which were far below the maximum residue limits set by the United States, the European Union and China. The limits of detection were calculated to be 2.98 μg/kg for flunixin in bovine muscle and 0.78 μg/L for 5-hydroxyflunixin in milk. In spike and recovery tests, the average recovery ranged from 83% to 105%, with a satisfying coefficient of variance ranging from 5.8% to 11.3%. Furthermore, the ELISA method was validated by a well-established LC-MS/MS method. These results proved that the established method is suitable for flunixin and 5-hydroxyflunixin residue analysis.
topic flunixin
5-hydroxyflunixin
immunoassay
bovine muscle
milk
url http://dx.doi.org/10.1080/09540105.2019.1577365
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AT shiminpeng developmentofanindirectcompetitiveenzymelinkedimmunosorbentassayfordetectingflunixinand5hydroxyflunixinresiduesinbovinemuscleandmilk
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