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首页> 外文期刊>Journal of food protection >Ochratoxin A: Comparison Of Extraction Methods From Grapes And Quantitative Determination By Different Competitive Enzyme-linked Immunosorbent Assay Kits
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Ochratoxin A: Comparison Of Extraction Methods From Grapes And Quantitative Determination By Different Competitive Enzyme-linked Immunosorbent Assay Kits

机译:ch曲霉毒素A:从葡萄中提取方法的比较和通过不同竞争性酶联免疫吸附测定试剂盒的定量测定

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The European Community has recently established a maximum limit for ochratoxin A (OTA) concentration in grapevine products, but many practical difficulties remain concerning the establishment of optimum cost-effective methods of quantification. The performance of four extraction procedures and three commercial competitive enzyme-linked immunosorbent assays (cELISAs) for grapes were compared. Results differed for the extractions and the cELISA kits. The advantage of using immunoaffinity columns (IACs) in the extraction was the excellent detection limit, which was between 0.06 and 0.0075 ng ml~(-1) depending on the cELISA kit used. Despite lower sensitivity (between 1.2 and 0.15 ng ml~(-1) depending on the cELISA kit), an extraction method in liquid phase, which was simple and inexpensive, was confirmed as suitable for quantifying OTA at levels estimated to be dangerous for human health. Two of the three cELISA kits produced satisfactory results. When these two cELISAs were coupled with IAC extraction, the lower quantification limits were 0.010 and 0.0075 ng ml~(-1), respectively, and the dynamic ranges were 50 and 27, respectively. The most reliable procedures were then compared with the reference method, high-performance liquid chromatography plus fluorescent detection coupled with an IAC. The results were very similar, although the cELISAs generally provided slightly higher values than did the chromatography method. The IAC method coupled with the cELISA was four times more sensitive than was the IAC method coupled with the chromatography method. The cELISA detection techniques were excellent alternatives to the already established chromatographic protocols, especially for mass screening and for determining concentrations of OTA as low as 0.010 ng ml~(-1).
机译:欧洲共同体最近为葡萄制品中的ra曲霉毒素A(OTA)浓度设定了最高限值,但是在建立最佳的经济有效的定量方法方面仍然存在许多实际困难。比较了四种提取程序和三种商用竞争性酶联免疫吸附法(cELISA)的葡萄性能。提取物和cELISA试剂盒的结果不同。提取中使用免疫亲和柱(IAC)的优势是极好的检测限,取决于所用的cELISA试剂盒,其检测限在0.06至0.0075 ng ml〜(-1)之间。尽管灵敏度较低(取决于cELISA试剂盒,灵敏度在1.2到0.15 ng ml〜(-1)之间),但液相萃取方法简便,廉价,被证实适用于定量估计对人体有害的OTA。健康。三种cELISA试剂盒中的两种产生了令人满意的结果。当这两种cELISAs结合IAC提取时,定量下限分别为0.010和0.0075 ng ml〜(-1),动态范围分别为50和27。然后将最可靠的程序与参考方法,高效液相色谱加IAC荧光检测相比较。结果非常相似,尽管cELISAs通常提供比色谱法稍高的值。 IAC方法与cELISA结合使用的灵敏度是IAC方法与色谱法结合使用的灵敏度的四倍。 cELISA检测技术是已建立的色谱方案的极佳替代方法,特别是用于质量筛选和测定低至0.010 ng ml〜(-1)的OTA浓度。

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