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Development and Application of a Quantitative Fluorescence-Based Immunochromatographic Assay for Fumonisin Bi in Maize

机译:玉米伏马菌素Bi荧光定量免疫色谱分析方法的开发与应用

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A fluorescence-based immunochromatographic assay (1CA) for fumonisin B, (FB,) that employs conjugates of fluorescent microspheres and monoclonal antibodies (FM—mAbs) as detection reporters is described. The 1CA is based on the competitive reaction between FB1-bovine serum albumin (BSA; test line) and the target FB1 for binding to the FM—mAb conjugates. A limit of detection (LOD) for FB1 of 0.12 ng/mL was obtained, with an analytical working range of 0.2S—2.0 ng/ mL (corresponding to 250—2000 μg/kg in maize flour samples, according to the extraction procedure). The recoveries of the ICA to detect FB[ in maize samples ranged from 91.4 to 118.2%. A quantitative comparison of the fluorescence-based 1CA and HPLC-MS/MS analysis of naturally contaminated maize samples indicated good agreement between the two methods (r~2 = 0.93). By replacing the target of interest, the FM-based ICA can easily be extended to other chemical contaminants and thus represents a versatile strategy for food safety analysis.
机译:描述了基于荧光的伏马菌素B(FB)的免疫色谱分析(1CA),采用荧光微球和单克隆抗体(FM-mAbs)的结合物作为检测报告基因。 1CA基于FB1牛血清白蛋白(BSA;测试线)与目标FB1之间与FM-mAb共轭物结合的竞争反应。 FB1的检出限(LOD)为0.12 ng / mL,分析工作范围为0.2S-2.0 ng / mL(根据提取程序,对应于玉米粉样品中的250-2000μg/ kg) 。用于检测玉米样品中FB [的ICA的回收率介于91.4%至118.2%之间。天然污染玉米样品的基于荧光的1CA和HPLC-MS / MS分析的定量比较表明,两种方法之间具有很好的一致性(r〜2 = 0.93)。通过替换感兴趣的目标,基于FM的ICA可以轻松扩展到其他化学污染物,因此代表了食品安全分析的通用策略。

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