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氯霉素的化学发光免疫分析

Chemiluminescence immunoassay for chloramphenicol.

作者信息

Lin Si, Han Shi-Quan, Liu Yi-Bing, Xu Wen-Ge, Guan Guo-Ying

机构信息

Isotope Department, China Institute of Atomic Energy, Beijing, 102413, R China.

出版信息

Anal Bioanal Chem. 2005 Jul;382(5):1250-5. doi: 10.1007/s00216-005-3273-6. Epub 2005 Jun 24.

Abstract

In recent years, various chemiluminescent clinical immunoassay kits have been widely applied to the detection of hormones. However, a kit for chloramphenicol (CAP) is often absent from most commercial product lists, even though it is important to control the levels of CAP residues in foodstuffs too. Therefore, we describe a simple, solid-phase chemiluminescence immunoassay (CLIA) for the measurement of CAP in foodstuffs. A rabbit anti-CAP IgG is passively adsorbed onto the walls of polypropylene plates. The labeled antigen is horseradish peroxidase (HRP) conjugate of CAP. Luminol solution is used as the substrate of HRP. The light yield is inversely proportional to the concentration of CAP. The method has a similar sensitivity (0.05 ng/ml), specificity, precision, and accuracy to a conventional enzyme immunoassay (EIA). The intra-assay and inter-assay CVs of ten samples were <8% and <20%, respectively, and the analytical recovery of the method was 87-100%. The experimental correlation coefficient of dilution was found to be 0.999 using milk supernatant as buffer. The detection limit for the method was 0.1-10 ng/ml, and it displayed good linearity.

摘要

近年来,各种化学发光临床免疫分析试剂盒已广泛应用于激素检测。然而,尽管控制食品中氯霉素(CAP)残留水平也很重要,但大多数商业产品清单中往往没有CAP检测试剂盒。因此,我们描述了一种用于测定食品中CAP的简单固相化学发光免疫分析(CLIA)方法。将兔抗CAP IgG被动吸附到聚丙烯板壁上。标记抗原是CAP的辣根过氧化物酶(HRP)偶联物。鲁米诺溶液用作HRP的底物。发光量与CAP浓度成反比。该方法与传统酶免疫分析(EIA)具有相似的灵敏度(0.05 ng/ml)、特异性、精密度和准确度。十个样品的批内和批间变异系数分别<8%和<20%,该方法的分析回收率为87-100%。以牛奶上清液为缓冲液时,稀释实验相关系数为0.999。该方法的检测限为0.1-10 ng/ml,线性良好。

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