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Highly Specific Chemiluminescence Immunoassay for the Determination of Chloramphenicol in Cosmetics

机译:高特异性化学发光免疫分析法测定化妆品中的氯霉素

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摘要

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 IC10, was 0.0021 ng mL−1. The detection range (IC20-IC80) 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.
机译:已经开发了一种直接和高度特异性的化学发光酶联免疫吸附测定(CL-ELISA)方法来监测化妆品中的氯霉素(CAP)。在这项工作中采用的用于直接免疫分析的抗氯霉素抗体(mAb)可以与CAP特异性结合,与大多数CAP类似物(包括与结构相关的噻吩酚(TAP)和氟苯尼考()具有相似的交叉反应性(CR)(小于0.01%)) FF)。通过IC10测得的检出限(LOD)为0.0021 ng mL -1 。检测范围(IC20-IC80)为0.00979至0.12026 ng mL -1 。在加标的化妆品样品中,平均回收率介于82.7%至99.6%之间,日内和日间差异分别小于9.8和8.2%。此外,借助HRP标记的抗CAP mAb,可以在快速直接免疫反应模式下处理该方法。这种CL-ELISA方法可用于化妆品中CAP的特异性,快速,半定量和定量检测,从而有助于CAP污染的精确质量控制。

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