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基于悬浮阵列免疫分析的谷物和饲料样品中多种霉菌毒素的同步定量测定

Simultaneous quantitative determination of multiple mycotoxins in cereal and feedstuff samples by a suspension array immunoassay.

作者信息

Wang Yuan-Kai, Yan Ya-Xian, Li Shu-Qing, Wang Heng-An, Ji Wen-Hui, Sun Jian-He

机构信息

Shanghai Key Laboratory of Veterinary Biotechnology, School of Agriculture and Biology, Shanghai Jiao Tong University , Shanghai 200240, China.

出版信息

J Agric Food Chem. 2013 Nov 20;61(46):10948-53. doi: 10.1021/jf4036029. Epub 2013 Nov 5.

Abstract

Mycotoxins produced by different species of fungi may coexist in single cereal and feedstuff samples, which could become highly toxic for humans and animals. In order to quantify four mycotoxins (zearalenone, fumonisin B1, deoxynivalenol, and aflatoxin B1) in cereal and feedstuff samples simultaneously, a new suspension array immunoassay was developed. Antimycotoxin monoclonal antibodies were conjugated to the surface of different encoding microspheres (19#, 37#, 39#, and 49#), and mycotoxin-protein conjugates were then coupled with biotin. Using streptavidin-phycoerythrin as a signal reporter protein, this direct competition multiple suspension array immunoassay was optimized. The results showed that the detection limits for zearalenone, fumonisin B1, deoxynivalenol, and aflatoxin B1 were 0.51, 6.0, 4.3, and 0.56 ng/mL, respectively, with detection ranges of 0.73-6.8, 11.6-110.3, 8.6-108.1, and 1.1-14.1 ng/mL, respectively. For the detection of the spiked samples, the recovery rates were between 92.3% and 115.5%. This method also shows a good correlation coefficient (r = 0.99, P < 0.01) with liquid chromatography-tandem mass spectrometry in the detection of toxins in commercial cereal and feedstuff samples. This suspension array immunoassay was high-throughput and accurate for the rapid quantitative detection of multiple mycotoxins in commercial cereal and feedstuff samples.

摘要

不同真菌物种产生的霉菌毒素可能共存于单一谷物和饲料样本中,这可能对人类和动物产生高毒性。为了同时定量谷物和饲料样本中的四种霉菌毒素(玉米赤霉烯酮、伏马毒素B1、脱氧雪腐镰刀菌烯醇和黄曲霉毒素B1),开发了一种新的悬浮阵列免疫分析法。抗霉菌毒素单克隆抗体与不同编码微球(19#、37#、39#和49#)的表面结合,然后将霉菌毒素-蛋白质偶联物与生物素偶联。使用链霉亲和素-藻红蛋白作为信号报告蛋白,对这种直接竞争多重悬浮阵列免疫分析法进行了优化。结果表明,玉米赤霉烯酮、伏马毒素B1、脱氧雪腐镰刀菌烯醇和黄曲霉毒素B1的检测限分别为0.51、6.0、4.3和0.56 ng/mL,检测范围分别为0.73 - 6.8、11.6 - 110.3、8.6 - 108.1和1.1 - 14.1 ng/mL。对于加标样本的检测,回收率在92.3%至115.5%之间。在商业谷物和饲料样本毒素检测中,该方法与液相色谱-串联质谱法也显示出良好的相关系数(r = 0.99,P < 0.01)。这种悬浮阵列免疫分析法用于商业谷物和饲料样本中多种霉菌毒素的快速定量检测,具有高通量和准确性。

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