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Highly Specific Chemiluminescence Immunoassay for the Determination of Chloramphenicol in Cosmetics

A direct and highly specific chemiluminescent enzyme-linked immunosorbent assay (CL-ELISA) method for monitoring chloramphenicol (CAP) in cosmetics has been developed. The anti-chloramphenicol antibody (mAb) adopted in this work for direct immunoassay could bind to CAP specifically, with negligible...

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Detalles Bibliográficos
Autores principales: Li, Qiyan, Zhu, Riran, Li, Jun, Wang, Xiaobing, Xu, Lihua, Li, Yanshen, Li, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609365/
https://www.ncbi.nlm.nih.gov/pubmed/31320903
http://dx.doi.org/10.1155/2019/7131907
Descripción
Sumario:A direct and highly specific chemiluminescent enzyme-linked immunosorbent assay (CL-ELISA) method for monitoring chloramphenicol (CAP) in cosmetics has been developed. The anti-chloramphenicol antibody (mAb) adopted in this work for direct immunoassay could bind to CAP specifically, with negligible cross-reactivity (CR) (less than 0.01%) with most CAP analogues, including structurally related thiamphenicol (TAP) and florfenicol (FF). The limit of detection (LOD), measured by IC(10), was 0.0021 ng mL(−1). The detection range (IC(20)-IC(80)) was ranged from 0.00979 to 0.12026 ng mL(−1). In spiked cosmetics samples, mean recoveries ranged from 82.7% to 99.6%, with intraday and interday variation less than 9.8 and 8.2%, respectively. Moreover, with the help of HRP-labeled anti-CAP mAb, the method could be processed in fast direct immunoreaction mode. This CL-ELISA method could be applied for specific, rapid, semiquantitative, and quantitative detection of CAP in cosmetics, facilitating the precise quality control of CAP contamination.