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Dual-label time-resolved fluoroimmunoassay for simultaneous detection of aflatoxin B1 and ochratoxin A

机译:双标记时间分辨荧光免疫分析法,可同时检测黄曲霉毒素B1和och曲毒素A

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摘要

A dual-label time-resolved fluoroimmunoassay (TRFIA) for simultaneous quantification of aflatoxin B1 (AFB1) and ochratoxin A (OTA) is described. For this, microtitration wells were coated with AFB1-horse radish peroxidase (HRP) and OTA–bovine serum albumin. The standards and samples were loaded on the coated plates, and diluted antibodies and Eu3+- and Sm3+-labeled IgG were then added. Our results showed that the sensitivity of TRFIA for AFB1 was 0.02 μg/L (range 0.02–100 μg/L). The intra- and inter-batch coefficient of variation (CV) was 3.2 and 7.3%, respectively, and the average recovery rate was 88.1%. On the other hand, the sensitivity of OTA was 0.05 μg/L (range 0.05–50 μg/L), the intra- and inter-batch CV was 2.9 and 7.9%, respectively, and the average recovery rate was 89.9%. In the AFB1/OTA–TRFIA, AFB1 and OTA did not mutually interfere. The correlation coefficients between the dual-label AFB1/OTA–TRFIA and the single-label AFB1–TRFIA or OTA–TRFIA were 0.972 and 0.981, respectively, indicating that the results were consistent. Our study suggests that AFB1/OTA–TRFIA allows the simultaneous detection of AFB1 and OTA; is a simple, fast, and economic method for screening large quantities of samples, and has good prospects of application.
机译:描述了一种用于同时定量黄曲霉毒素B1(AFB1)和曲霉毒素A(OTA)的双标记时间分辨荧光免疫测定(TRFIA)。为此,在微量滴定孔上涂上AFB1辣根过氧化物酶(HRP)和OTA-牛血清白蛋白。将标准品和样品上样到包被的板上,然后加入稀释的抗体以及Eu 3 + -和Sm 3 + 标记的IgG。我们的结果表明,TRFIA对AFB1的敏感性为0.02μg/ L(范围为0.02–100μg/ L)。批内和批间变异系数(CV)分别为3.2%和7.3%,平均回收率为88.1%。另一方面,OTA的灵敏度为0.05μg/ L(范围为0.05–50μg/ L),批内和批间CV分别为2.9%和7.9%,平均回收率为89.9%。在AFB1 / OTA-TRFIA中,AFB1和OTA互不干扰。双标签AFB1 / OTA-TRFIA与单标签AFB1-TRFIA或OTA-TRFIA之间的相关系数分别为0.972和0.981,表明结果是一致的。我们的研究表明,AFB1 / OTA-TRFIA可以同时检测AFB1和OTA。是一种简便,快速,经济的筛查大量样品的方法,具有良好的应用前景。

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