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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Development of two enzyme-linked immunosorbent assays for detection of endosulfan residues in agricultural products
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Development of two enzyme-linked immunosorbent assays for detection of endosulfan residues in agricultural products

机译:两种用于检测农产品中硫丹残留的酶联免疫吸附测定方法的开发

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Two competitive immunoassays, a laboratory assay based on microwell plates and a field test based on the use of polystyrene tubes, have been developed for the detection of endosulfan in agricultural products. The limit of detection for the microwell plate format was 0.8 +/- 0.1 mu g/kg, and the limit of detection for the tube format was 1.6 +/- 0.2 mu g/kg. A simple, rapid, and efficient extraction method was employed, and 76-112% recoveries of spiked samples were obtained. Methanol extracts of some agricultural product samples such as grape, carrot, spinach, and tobacco could be analyzed directly by immunoassay after dilution in 0.5% fish skin gelatin-phosphate buffered saline. In contrast, extracts of green tea caused significant interference in the assay, and a number of simple cleanup methods were ineffective in removing interference. However, use of the coagulating reagent polyvinyl pyrrolidone removed the matrix effect effectively. For the validation of the enzyme-linked immunosorbent assay (ELISA) tests, samples were analyzed by ELISA and gas chromatography (GC) after solid phase extraction. The relationship between data obtained using the tube assay and microwell assay was good (the lowest r(2) value was 0.94), and also, the immunoassay assay data correlated well with data obtained from GC analysis (the lowest r(2) value was 0.93). The developed immunoassay methods are the suitable methods for the rapid quantitative and reliable determination of endosulfan residues in agricultural products.
机译:已经开发了两种竞争性免疫测定法,一种基于微孔板的实验室测定法和一种基于聚苯乙烯管使用的现场试验,用于检测农产品中的硫丹。微孔板形式的检测限为0.8 +/- 0.1μg / kg,管形形式的检测限为1.6 +/- 0.2μg / kg。采用了一种简单,快速,有效的提取方法,加标样品的回收率达到76-112%。在0.5%鱼皮明胶-磷酸盐缓冲液中稀释后,可以通过免疫分析法直接分析某些农产品样品(例如葡萄,胡萝卜,菠菜和烟草)的甲醇提取物。相比之下,绿茶提取物在测定中造成了显着干扰,许多简单的净化方法在消除干扰方面均无效。然而,使用凝结剂聚乙烯吡咯烷酮有效地消除了基质效应。为了验证酶联免疫吸附测定(ELISA)测试,固相萃取后通过ELISA和气相色谱(GC)分析样品。使用试管法和微孔测定法获得的数据之间的关系很好(最低的r(2)值为0.94),而且免疫测定法的数据与通过GC分析获得的数据具有很好的相关性(最低的r(2)值为0.93)。发达的免疫测定方法是用于快速定量和可靠测定农产品中硫丹残留量的合适方法。

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