An ultrasensitive electrochemical DNA biosensor based on a copper oxide nanowires/single-walled carbon nanotubes nanocomposite

被引:35
作者
Chen, Mei [1 ]
Hou, Changjun [1 ,2 ]
Huo, Danqun [1 ,2 ]
Yang, Mei [1 ]
Fa, Huanbao [3 ]
机构
[1] Chongqing Univ, Coll Bioengn, Key Lab Biorheol Sci & Technol, Minist Educ, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Natl Key Lab Fundamental Sci Micro Nano Device &, Chongqing 400044, Peoples R China
[3] Chongqing Univ, Coll Chem & Chem Engn, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical; CuO nanowire; Single-walled carbon nanotube; Ad riamyc in; Differential pulse voltammetry; DNA biosensor; REAL-TIME DETECTION; MOLECULAR BEACON; ENZYME-FREE; GLUCOSE; NANOPARTICLES; AMPLIFICATION; VIRUS; ASSAY;
D O I
10.1016/j.apsusc.2015.12.203
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Here, we developed a novel and sensitive electrochemical biosensor to detect specific-sequence target DNA. The biosensor was based on a hybrid nanocomposite consisting of copper oxide nanowires (CuO NWs) and carboxyl-functionalized single-walled carbon nanotubes (SWCNTs-COOH). The resulting CuO NWs/SWCNTs layers exhibited a good differential pulse voltammetry (DPV) current response for the target DNA sequences, which we attributed to the properties of CuO NWs and SWCNTs. CuO NWs and SWCNTs hybrid composites with highly conductive and biocompatible nanostructure were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and cyclic voltammetry (CV). Immobilization of the probe DNA on the electrode surface was largely improved due to the unique synergetic effect of CuO NWs and SWCNTs. DPV was applied to monitor the DNA hybridization event, using adriamycin as an electrochemical indicator. Under optimal conditions, the peak currents of adriamycin were linear with the logarithm of target DNA concentrations (ranging from 1.0 x 10(-14) to 1.0 x 10(-8) M), with a detection limit of 3.5 x 10(-15) M (signal/noise ratio of 3). The biosensor also showed high selectivity to single-base mismatched target DNA. Compared with other electrochemical DNA biosensors, we showed that the proposed biosensor is simple to implement, with good stability and high sensitivity. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:703 / 709
页数:7
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