首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Photoelectrochemical immunoassay of aflatoxin B-1 in foodstuff based on amorphous TiO2 and CsPbBr3 perovskite nanocrystals
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Photoelectrochemical immunoassay of aflatoxin B-1 in foodstuff based on amorphous TiO2 and CsPbBr3 perovskite nanocrystals

机译:基于无定形TiO2和CSPBBR3 Perovskite纳米晶体食品中黄曲霉毒素B-1的光电化学免疫测定

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摘要

Aflatoxin B-1 (AFB(1)) pollution is one of the most serious problems for food safety. In this paper, a split-type photoelectrochemical (PEC) immunoassay was designed for sensitive detection of AFB(1) in foodstuffs by using amorphous TiO2 with all-inorganic perovskite CsPbBr3 nanocrystals (CsPbBr3/a-TiO2). The a-TiO2 layer not only improved the stability of CsPbBr3 nanocrystals, but also facilitated charge transfer, which resulted in the increasing photocurrent of the nanocomposites. Initially, a competitive-type enzyme immunoreaction was executed on a high-binding microplate between the analyte and alkaline phosphatase (ALP)-labeled AFB(1)-bovine serum albumin (AFB(1)-BSA) conjugate. Accompanied by the formation of the immunocomplex, the carried ALP triggered enzymatic hydrolysis to generate ascorbic acid (AA, as an electron donor) for increasing the photocurrent of the CsPbBr3/a-TiO2-modified electrode. Coupling with the competitive enzyme immunoassay, the photocurrent of the modified electrode decreased with the increase of target AFB(1) concentration in a dynamic working range from 0.01 ng mL(-1) to 15 ng mL(-1) with a limit of detection (LOD) of 2.8 pg mL(-1) under optimum conditions. Furthermore, the photoelectrochemical immunoassay was also utilized to detect AFB(1) in peanut and corn samples, giving acceptable accuracy in comparison with the referenced AFB(1) enzyme-linked immunosorbent assay (ELISA) method.
机译:黄曲霉毒素B-1(AFB(1))污染是食品安全最严重的问题之一。本文通过使用无机钙钛矿CSPBBR3纳米晶(CSPBBR3 / A-TiO2),设计了一种分裂式光电化学(PEC)免疫测定法用于通过使用无机钙钛矿CSPBBR3纳米晶体(CSPBBR3 / A-TiO2)的无定形TiO2在食品中的敏感检测。 A-TiO2层不仅提高了CSPBBR3纳米晶体的稳定性,而且还促进了电荷转移,这导致纳米复合材料的光电流增加。最初,在分析物和碱性磷酸酶(ALP) - 标记的AFB(1)颗粒血清白蛋白(AFB(1)-BSA)缀合物之间的高结合微孔板上在高结合的微孔板上执行竞争型酶免疫反应。伴随着免疫激散的形成,所携带的ALP触发酶水解以产生抗坏血酸(AA,作为电子供体),用于增加CSPBBR3 / A-TiO2改性电极的光电流。与竞争性酶免疫测定的偶联,改性电极的光电流随着动态工作范围内的靶AFB(1)浓度的增加而下降,从0.01 ng ml(-1)至15ng ml(-1),具有检测限(LOD)在最佳条件下为2.8 pg ml(-1)。此外,光电化学免疫测定还用于检测花生和玉米样品中的AFB(1),与参考的AFB(1)酶联免疫吸附测定(ELISA)方法相比,可接受的精度。

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