首页> 外文期刊>Analytica chimica acta >Etching reaction-based photoelectrochemical immunoassay of aflatoxin B-1 in foodstuff using cobalt oxyhydroxide nanosheets-coating cadmium sulfide nanoparticles as the signal tags
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Etching reaction-based photoelectrochemical immunoassay of aflatoxin B-1 in foodstuff using cobalt oxyhydroxide nanosheets-coating cadmium sulfide nanoparticles as the signal tags

机译:使用钴羟基氧化物纳米晶片 - 硫化镉纳米粒子作为信号标签,蚀刻食品中黄曲霉毒素B-1的基于反应的光电子化学免疫测定。

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A new split-type photoelectrochemical (PEC) immunosensing platform was designed for sensitive detection of aflatoxin B-1 (AFB(1)) in foodstuffs, coupling with enzymatic hydrolysate-triggered etching reaction of cobalt oxyhydroxide (CoOOH) on cadmium sulfide (CdS) nanoparticles-functionalized interface. Initially, the photosensitive electrode was prepared by coating CoOOH nanosheets on the surface of CdS nanoparticles to quench the photocurrent. Thereafter, a competitive- type enzyme immunoreaction was carried out on monoclonal anti-AFB(1) antibody-conjugated magnetic bead by using alkaline phosphatase (ALP)-labeled bovine serum albumin-AFB(1) (AFB(1)-BSA) conjugate as the competitor. With the formation of immunocomplex, the carried ALP hydrolyzed ascorbic acid 2-phosphate (AAP) into ascorbic acid (AA) and phosphate. The former ascorbic acid produced etched or dissolved CoOOH nanosheets into Co2+ ions, thus resulting in the exposure of CdS nanoparticles on the surface to enhance the photocurrent of the modified electrode. Under optimum conditions, the photocurrent decreased linearly with the increasing AFB(1) concentration in the dynamic range of 0.01-10 ng mL(-1), and the limit of detection was 2.6 pg mL(-1). The precision of this method (expressed as RSD) was +/- 8.6%. In addition, the accuracy was monitored by analyzing spiked food samples, and gave the well-matched results with the referenced ELISA method. (C) 2018 Elsevier B.V. All rights reserved.
机译:设计了一种新的分流式光电化学(PEC)免疫抑制平台,用于食品中的黄曲霉毒素B-1(AFB(1))的敏感检测,与硫化镉(CDS)上的钴羟基氧化物(COOH)的酶水解 - 触发蚀刻反应偶联纳米粒子官能化界面。最初,通过在CDS纳米颗粒表面上涂覆CoOOH纳米片来制备光敏电极以淬灭光电流​​。此后,通过使用碱性磷酸酶(ALP) - 标记的牛血清白蛋白-AFB(1)(AFB(1)-BSA)缀合物对单克隆抗-FB(1)抗体 - 缀合的磁珠进行竞争型酶免疫反应。缀合物作为竞争对手。随着Immunocomplex的形成,所携带的ALP将抗坏血酸2-磷酸(AAP)水解成抗坏血酸(AA)和磷酸盐。将前一种抗坏血酸产生蚀刻或溶解的COOH纳米片中成CO 2 +离子,从而导致CDS纳米颗粒在表面上暴露以增强改性电极的光电流。在最佳条件下,光电流随着0.01-10 ng ml(-1)的动态范围内的增加的AFB(1)浓度线性降低,并且检测限为2.6pg ml(-1)。该方法的精确度(表示为RSD)是+/- 8.6%。此外,通过分析尖刺的食物样品来监测精度,并通过参考的ELISA方法给出良好匹配的结果。 (c)2018 Elsevier B.v.保留所有权利。

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