检出限
化学
微分脉冲伏安法
适体
生物传感器
黄曲霉毒素
纳米材料
线性范围
Zeta电位
胶体金
电极
伏安法
循环伏安法
电化学
树枝状大分子
核化学
分析化学(期刊)
组合化学
电子转移
色谱法
荧光
表面等离子共振
纳米颗粒
电化学气体传感器
纳米技术
X射线光电子能谱
方波
作者
Xinran Yang,Chuanjin Cui,Hongshuo Chen
标识
DOI:10.1002/cbdv.202502574
摘要
ABSTRACT Developing a reliable detection method for aflatoxin B 1 (AFB 1 ) is urgent due to its potent hepatocarcinogenic effects. An electrochemical aptamer sensor based on competitive binding was prepared for the rapid detection of AFB 1 in this study. Poly(amideamine) dendrimers were electrodeposited onto a screen‐printed gold electrode to enhance aptamer loading via amine group conjugation. The chemically synthesized gold nanostars can further improve electron transfer kinetics and provide additional binding sites for single‐stranded DNA probes. Bioprobe and modified electrode were comprehensively characterized by transmission electron microscope, scanning electron microscopy, Zeta potential, energy dispersive spectroscopy, selected area electron diffraction, X‐ray photoelectron spectroscopy, and atomic force microscope. Differential pulse voltammetry (DPV) and square wave voltammetry (SWV) of pulse voltametric techniques were executed separately in AFB1 solutions for testing the performance of this prepared biosensor. Comparative analysis revealed that both methods exhibited a linear detection range of 10 −4 to 10 3 ng/mL for AFB 1 . Nevertheless, the DPV method achieved a lower limit of 2.25 × 10 −5 ng/mL than the SWV method, with a detection limit of 3.18 × 10 −5 ng/mL. Meanwhile, the developed biosensor showed excellent stability and reproducibility, establishing its reliability for AFB 1 quantification in complex matrices.
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