Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs
An ultrasensitive monoclonal antibody-based gold nanoparticle immunochromatographic strip assay and indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) were developed to detect florfenicol (FF) and thiamphenicol (TAP) in egg samples. The ic-ELISA, with optimized pH, methanol content an...
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doaj-5c137e9e6a324abf99a9480f8d6246282020-11-25T01:57:16ZengTaylor & Francis GroupFood and Agricultural Immunology0954-01051465-34432018-01-0129125426610.1080/09540105.2017.13711141371114Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggsXianlu Lei0Liguang Xu1Shanshan Song2Liqiang Liu3Hua Kuang4Jiangnan UniversityJiangnan UniversityJiangnan UniversityJiangnan UniversityJiangnan UniversityAn ultrasensitive monoclonal antibody-based gold nanoparticle immunochromatographic strip assay and indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) were developed to detect florfenicol (FF) and thiamphenicol (TAP) in egg samples. The ic-ELISA, with optimized pH, methanol content and sodium chloride content, exhibited an IC50 value of 0.2 ng/mL for FF and 0.27 ng/mL for TAP, with the working range of 0.05–0.77 and 0.05–1.42 ng/mL, respectively. The optimized ic-ELISA showed negligible cross-reactivity with other phenols and broad-spectrum antibiotics. The recoveries in egg samples using the ic-ELISA ranged from 84% to 115% with a coefficient of variation of less than 5%. Based on this monoclonal antibody, a rapid and ultrasensitive immunochromatographic strip assay was developed with a cutoff value of 1 ng/mL for FF and TAP. Our results indicated that both developed methods were highly useful for screening FF and TAP in eggs.http://dx.doi.org/10.1080/09540105.2017.1371114florfenicolic-elisaimmunochromatographic strip assaymonoclonal antibodythiamphenicol |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xianlu Lei Liguang Xu Shanshan Song Liqiang Liu Hua Kuang |
spellingShingle |
Xianlu Lei Liguang Xu Shanshan Song Liqiang Liu Hua Kuang Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs Food and Agricultural Immunology florfenicol ic-elisa immunochromatographic strip assay monoclonal antibody thiamphenicol |
author_facet |
Xianlu Lei Liguang Xu Shanshan Song Liqiang Liu Hua Kuang |
author_sort |
Xianlu Lei |
title |
Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs |
title_short |
Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs |
title_full |
Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs |
title_fullStr |
Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs |
title_full_unstemmed |
Development of an ultrasensitive ic-ELISA and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs |
title_sort |
development of an ultrasensitive ic-elisa and immunochromatographic strip assay for the simultaneous detection of florfenicol and thiamphenicol in eggs |
publisher |
Taylor & Francis Group |
series |
Food and Agricultural Immunology |
issn |
0954-0105 1465-3443 |
publishDate |
2018-01-01 |
description |
An ultrasensitive monoclonal antibody-based gold nanoparticle immunochromatographic strip assay and indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) were developed to detect florfenicol (FF) and thiamphenicol (TAP) in egg samples. The ic-ELISA, with optimized pH, methanol content and sodium chloride content, exhibited an IC50 value of 0.2 ng/mL for FF and 0.27 ng/mL for TAP, with the working range of 0.05–0.77 and 0.05–1.42 ng/mL, respectively. The optimized ic-ELISA showed negligible cross-reactivity with other phenols and broad-spectrum antibiotics. The recoveries in egg samples using the ic-ELISA ranged from 84% to 115% with a coefficient of variation of less than 5%. Based on this monoclonal antibody, a rapid and ultrasensitive immunochromatographic strip assay was developed with a cutoff value of 1 ng/mL for FF and TAP. Our results indicated that both developed methods were highly useful for screening FF and TAP in eggs. |
topic |
florfenicol ic-elisa immunochromatographic strip assay monoclonal antibody thiamphenicol |
url |
http://dx.doi.org/10.1080/09540105.2017.1371114 |
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