Ultrasensitive electrochemical sensor for Hg2+ by using hybridization chain reaction coupled with Ag@Au core-shell nanoparticles

被引:53
作者
Li, Zongbing [1 ]
Miao, Xiangmin [1 ]
Xing, Ke [1 ]
Peng, Xue [1 ]
Zhu, Aihua [1 ]
Ling, Liansheng [2 ]
机构
[1] Jiangsu Normal Univ, Sch Life Sci, Xuzhou 221116, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical sensor; Hg2+ detection; Hybridization chain reaction; Positively charged Ag@Au core-shell; nanoparticles; FLUORESCENT SENSOR; QUANTUM DOTS; SILVER NANOPARTICLES; GOLD NANOPARTICLES; VISUAL DETECTION; IONS; AMPLIFICATION; MERCURY(II); NANOCLUSTERS; IMMUNOASSAY;
D O I
10.1016/j.bios.2016.01.074
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel electrochemical biosensor for Hg2+ detection was reported by using DNA-based hybridization chain reaction (HCR) coupled with positively charged Ag@Au core-shell nanoparticles ((+)Ag@Au CSNPs) amplification. To construct the sensor, capture probe (CP) was firstly immobilized onto the surface of glass carbon electrode (GCE). In the presence of Hg2+, the sandwiched complex can be formed between the immobilized CP on the electrode surface and the detection probe (DP) modified on the gold nano particles (AuNPs) based on T-Hg2+-T coordination chemistry. The carried DP then opened two ferrocene (Fc) modified hairpin DNA (H-1 and H-2) in sequence and propagated the happen of HCR to form a nicked double-helix. Numerous Fc molecules were formed on the neighboring probe and produced an obvious electrochemical signal. Moreover, (+)Ag@Au CSNPs were assembly onto such dsDNA polymers as electrochemical signal enhancer. Under optimal conditions, such sensor presents good electrochemical responses for Hg2+ detection with a detection limit of 3.6 pM. Importantly, the methodology has high selectivity for Hg2+ detection. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:339 / 343
页数:5
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