电极
胶体金
化学
适体
检出限
介电谱
生物传感器
电子转移
电化学
Mercury(编程语言)
寡核苷酸
分析化学(期刊)
线性范围
纳米技术
纳米颗粒
材料科学
光化学
环境化学
色谱法
物理化学
DNA
生物
生物化学
遗传学
计算机科学
程序设计语言
作者
Ying Gan,Jiadi Sun,Tao Liang,Jiawei Tu,Ning Hu,Hao Wan,Ping Wang
摘要
Heavy metal contamination in aquatic environment has made great adverse impacts on human health and environment. In this work, a label-free electrochemical gold nanoband aptasensor (GNA) was developed using thymine-Hg2+-thymine (T-Hg2+-T) coordination chemistry for Hg2+ detection in drinking water. The gold nanoband sensor contains gold nanoband working electrode with a band thickness of 100 nm. The nanoscale working electrode increases the mass transfer rate and sensitivity for Hg2+ detection. Moreover, the gold nanoband sensors are cost-effective and can be easily regenerated by cutting the edge after the performance decreases dramatically compared with microelectrodes and disk electrodes. T-rich oligonucleotides modified with thiol group was self-assembled onto the working electrode through Au-S covalent bonding. In the presence of Hg2+, oligonucleotides will capture Hg2+, thus inducing the conformational change from single-strand to duplex-like structure that would promote electron transfer. Electrochemical impedance spectroscopy (EIS) was used to detect the Hg2+-mediated conformational changes. By optimizing experimental conditions, the linear range of proposed biosensor is from 0.1 nM to 1 μM, and the limit of detection is 40 pM (8 ppt). Furthermore, this nanobiosensors exhibited high selectivity and a great potential to detect trace Hg2+ in real samples from aquatic environment.
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