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Magnetic Bead-Based Colorimetric Immunoassay for Aflatoxin B1 Using Gold Nanoparticles

机译:基于金纳米粒子的基于磁珠的黄曲霉毒素B1比色免疫测定

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摘要

A competitive colorimetric immunoassay for the detection of aflatoxin B1 (AFB) has been established using biofunctionalized magnetic beads (MBs) and gold nanoparticles (GNPs). Aflatoxin B1-bovine serum albumin conjugates (AFB-BSA) modified MBs were employed as capture probe, which could specifically bind with GNP-labeled anti-AFB antibodies through immunoreaction, while such specific binding was competitively inhibited by the addition of AFB. After magnetic separation, the supernatant solution containing unbound GNPs was directly tested by UV-Vis spectroscopy. The absorption intensity was directly proportional to the AFB concentration. The influence of GNP size, incubation time and pH was investigated in detail. After optimization, the developed method could detect AFB in a linear range from 20 to 800 ng/L, with the limit of detection at 12 ng/L. The recoveries for spiked maize samples ranged from 92.8% to 122.0%. The proposed immunoassay provides a promising approach for simple, rapid, specific and cost-effective detection of toxins in the field of food safety.
机译:已经使用生物功能化的磁珠(MBs)和金纳米颗粒(GNPs)建立了用于检测黄曲霉毒素B1(AFB)的竞争性比色免疫测定法。黄曲霉毒素B1牛血清白蛋白偶联物(AFB-BSA)修饰的MBs被用作捕获探针,可通过免疫反应与GNP标记的抗AFB抗体特异性结合,而这种特异性结合可通过添加AFB竞争性抑制。磁分离后,通过紫外-可见光谱法直接测试含有未结合的GNP的上清液。吸收强度与AFB浓度成正比。详细研究了GNP大小,孵育时间和pH值的影响。经过优化后,所开发的方法可以在20至800 ng / L的线性范围内检测AFB,检测极限为12 ng / L。加标玉米样品的回收率在92.8%至122.0%之间。所提出的免疫测定法为食品安全领域中毒素的简单,快速,特异性和成本有效的检测提供了一种有前途的方法。

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