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Aflatoxin B1 Detection Using a Highly-Sensitive Molecularly-Imprinted Electrochemical Sensor Based on an Electropolymerized Metal Organic Framework

机译:基于电聚合金属有机骨架的高灵敏度分子印迹电化学传感器检测黄曲霉毒素B1

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摘要

A sensitive electrochemical molecularly-imprinted sensor was developed for the detection of aflatoxin B1 (AFB1), by electropolymerization of p-aminothiophenol-functionalized gold nanoparticles in the presence of AFB1 as a template molecule. The extraction of the template leads to the formation of cavities that are able to specifically recognize and bind AFB1 through π-π interactions between AFB1 molecules and aniline moities. The performance of the developed sensor for the detection of AFB1 was investigated by linear sweep voltammetry using a hexacyanoferrate/hexacyanoferrite solution as a redox probe, the electron transfer rate increasing when the concentration of AFB1 increases, due to a p-doping effect. The molecularly-imprinted sensor exhibits a broad linear range, between 3.2 fM and 3.2 µM, and a quantification limit of 3 fM. Compared to the non-imprinted sensor, the imprinting factor was found to be 10. Selectivity studies were also performed towards the binding of other aflatoxins and ochratoxin A, proving good selectivity.
机译:通过在AFB1作为模板分子存在下对氨基苯硫酚官能化的金纳米粒子进行电聚合,开发了一种灵敏的电化学分子印迹传感器,用于检测黄曲霉毒素B1(AFB1)。模板的提取导致形成空腔,该空腔能够通过AFB1分子与苯胺分子之间的π-π相互作用特异性识别并结合AFB1。通过线性扫描伏安法,使用六氰基铁酸盐/六氰基铁氧体溶液作为氧化还原探针,研究了开发的用于检测AFB1的传感器的性能,由于p掺杂效应,当AFB1的浓度增加时,电子传输速率增加。分子印迹传感器具有3.2 fM至3.2 µM的宽线性范围,定量限为3 fM。与非印迹传感器相比,印迹因子为10。还针对其他黄曲霉毒素和and曲霉毒素A的结合进行了选择性研究,证明了良好的选择性。

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