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基于在负载金纳米粒子的电极上使用负载银纳米粒子的标记物对硫堇电化学进行双信号增强的脱氧雪腐镰刀菌烯醇选择性适配体传感器。

Selective aptasensor of deoxynivalenol based on dual signal enhancement of thionine electrochemistry using silver nanoparticle-loaded label at gold nanoparticle-loaded electrodes.

作者信息

Cui Xiaoying, Zhao Ke, Qu Zhengquan, Chao Xipeng, Xie Lingling, Chen Hanyu, He Baoshan, Zhang Baozhong

机构信息

School of Environmental Engineering, Henan University of Technology, Lianhua Road 100#, Zhengzhou 450001, Henan Province, People's Republic of China.

School of Food Science and Technology, Henan University of Technology, Lianhua Road 100#, Zhengzhou 450001, Henan Province, People's Republic of China.

出版信息

Bioelectrochemistry. 2025 Jun;163:108881. doi: 10.1016/j.bioelechem.2024.108881. Epub 2024 Dec 9.

DOI:10.1016/j.bioelechem.2024.108881
PMID:39657431
Abstract

In this work, an efficient sensing platform deoxynivalenol (DON) detection was constructed through monitoring the current change of a competitive mechanism triggered by DON, leading the signal label detached from the electrode surface by square-wave voltammetry using thionine (Thi) as a redox indicator. The complementary strand of aptamer (cDNA) and Thi were loaded onto Fe/Ni bimetallic metal-organic framework loaded with sliver nanoparticles (AgNPs@FeNi-MOF) to construct AgNPs@FeNi-MOF/cDNA/Thi signal probes. In the presence of DON, the aptamer sequence was more predisposed to form an aptamer-DON complex, resulting in the displacement of the cDNA. The signal probe was subsequently released, leading to a decrease in the signal intensity of Thi. Notably, AgNPs@FeNi-MOF has a larger electroactive specific surface area and is able to load more cDNA and thi, which can amplify the signal. Under the optimal experimental conditions, the developed sensor exhibits a good linear response in the range of 1 × 10 to 1 × 10 pg/mL, with a limit of detection (LOD) of 5.68 fg/mL and has good selectivity, reproducibility and stability.

摘要

在本工作中,通过监测由脱氧雪腐镰刀菌烯醇(DON)触发的竞争机制的电流变化,构建了一种高效的DON传感平台,利用硫堇(Thi)作为氧化还原指示剂,通过方波伏安法使信号标签从电极表面脱离。将适配体互补链(cDNA)和Thi负载到负载有银纳米颗粒的铁/镍双金属金属有机框架(AgNPs@FeNi-MOF)上,构建AgNPs@FeNi-MOF/cDNA/Thi信号探针。在DON存在的情况下,适配体序列更倾向于形成适配体-DON复合物,导致cDNA被取代。随后信号探针被释放,导致Thi的信号强度降低。值得注意的是,AgNPs@FeNi-MOF具有更大的电活性比表面积,能够负载更多的cDNA和Thi,从而可以放大信号。在最佳实验条件下,所开发的传感器在1×10至1×10 pg/mL范围内表现出良好的线性响应,检测限(LOD)为5.68 fg/mL,具有良好的选择性、重现性和稳定性。

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