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Specific Monoclonal Antibody-Based Enzyme Immunoassay for Sensitive and Reliable Detection of Alternaria Mycotoxin Iso-Tenuazonic Acid in Food Products

机译:基于特异性单克隆抗体的酶联免疫分析法可灵敏可靠地检测食品中的链霉菌霉菌毒素异丁酸。

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摘要

In this paper, we report the development of a sensitiveand specific monoclonal antibody-based immunodiagnosticmethod for the detection of iso-tenuazonic acid (ITeA),an Alternaria mycotoxin, in food samples. The ITeA wasderivatized with hydrazine hydrate to produce the antigen(E)-3-(1-hydrazonoethyl)-4-hydroxy-5-isobutyl-1H-pyrrol-2(5H)-one (ITeAH) which was further reacted with glyoxalicacid to generate the hapten (E)-2-((Z)-(1-(4-hydroxy-5-isobutyl-2-oxo-2,5-dihydro-1H-pyrrol-3-yl)ethylidene)(ITeAHGA) which was used as an immunogen after conjugationto bovine serum albumin (BSA). A highly specific monoclonalantibody selectively binding to ITeAH was generatedvia the hybridoma technique and subsequently used to constructa heterologous indirect competitive enzyme-linked immunosorbentassay (icELISA) using ITeAH as the competitiveantigen for the detection of ITeA with a limit of detection(LOD) of 0.5 ng/mL. Under the optimum conditions, the developedicELISA is highly sensitive (IC50 = 7.8 ng/mL) withrecovery rates ranged from 82.3 to 109.8% for spiked foodsamples. The comparative analysis of results revealed a goodcorrelation between the icELISA and the standard HPLC-MS/MS method, confirming the suitability of the developedicELISA for screening and detection of mycotoxin ITeA infood samples.
机译:在本文中,我们报告了一种基于敏感性和特异性的基于单克隆抗体的免疫诊断方法的开发,该方法可用于检测食物样品中的链格孢霉菌毒素异戊二酸(ITeA)。用水合肼将ITeA衍生化以产生抗原(E)-3-(1-肼基乙基)-4-羟基-5-异丁基-1H-吡咯-2(5H)-一(ITeAH),该抗原进一步与乙二酸反应生成生成半抗原(E)-2-((Z)-(1-(4-羟基-5-异丁基-2-氧代-2,5-二氢-1H-吡咯-3-基)亚乙基)(ITeAHGA)牛血清白蛋白(BSA)结合后用作免疫原,通过杂交瘤技术产生选择性结合ITeAH的高度特异性单克隆抗体,随后用于构建以ITeAH为竞争性抗原的异源间接竞争性酶联免疫吸附法(icELISA)。 ITeA的检出限(LOD)为0.5 ng / mL。在最佳条件下,发达的ELISA具有很高的灵敏度(IC50 = 7.8 ng / mL),加标食品样品的回收率在82.3%至109.8%之间。结果显示icELISA与标准HPLC-MS / MS方法之间具有良好的相关性,从而证实了发育性ELISA适于筛查和检测食品样品中的霉菌毒素ITeA。

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