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Electrochemical Immunosensor Based on Polythionine/Gold Nanoparticles for the Determination of Aflatoxin B1

机译:基于聚蛋氨酸/金纳米颗粒的电化学免疫传感器测定黄曲霉毒素B1

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摘要

An aflatoxin B1 (AFB1) electrochemical immunosensor was developed by the immobilisation of aflatoxin B1-bovine serum albumin (AFB1-BSA) conjugate on a polythionine (PTH)/gold nanoparticles (AuNP)-modified glassy carbon electrode (GCE). The surface of the AFB1-BSA conjugate was covered with horseradish peroxidase (HRP), in order to prevent non-specific binding of the immunosensors with ions in the test solution. The AFB1 immunosensor exhibited a quasi-reversible electrochemistry as indicated by a cyclic voltammetric (CV) peak separation (ΔEp) value of 62 mV. The experimental procedure for the detection of AFB1 involved the setting up of a competition between free AFB1 and the immobilised AFB1-BSA conjugate for the binding sites of free anti-aflatoxin B1 (anti-AFB1) antibody. The immunosensor's differential pulse voltammetry (DPV) responses (peak currents) decreased as the concentration of free AFB1 increased within a dynamic linear range (DLR) of 0.6 - 2.4 ng/mL AFB1 and a limit of detection (LOD) of 0.07 ng/mL AFB1. This immunosensing procedure eliminates the need for enzyme-labeled secondary antibodies normally used in conventional ELISA–based immunosensors.
机译:黄曲霉毒素B1(AFB1)电化学免疫传感器是通过将黄曲霉毒素B1牛血清白蛋白(AFB1-BSA)共轭物固定在聚硫氨酸(PTH)/金纳米颗粒(AuNP)修饰的玻碳电极(GCE)上而开发的。为了防止免疫传感器与测试溶液中的离子发生非特异性结合,AFB1-BSA共轭物的表面覆盖有辣根过氧化物酶(HRP)。 AFB1免疫传感器表现出准可逆的电化学反应,如循环伏安(CV)峰分离(ΔEp)值为62 mV所示。检测AFB1的实验程序涉及建立游离AFB1与固定化AFB1-BSA偶联物之间的竞争,以竞争游离抗黄曲霉毒素B1(抗AFB1)抗体的结合位点。随着游离AFB1浓度在0.6-2.4 ng / mL动态线性范围(DLR)和0.07 ng / mL的检出限(LOD)内增加,免疫传感器的差分脉冲伏安法(DPV)响应(峰值电流)降低AFB1。这种免疫传感程序消除了通常在传统的基于ELISA的免疫传感器中使用的酶标二抗的需要。

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