Label-free electrochemical DNA biosensor for rapid detection of mutidrug resistance gene based on Au nanoparticles/toluidine blue-graphene oxide nanocomposites

被引:132
作者
Peng, Hua-Ping [1 ,3 ]
Hu, Yan [1 ,3 ]
Liu, Pan [1 ,3 ]
Deng, Ya-Ni [1 ,3 ]
Wang, Peng [1 ,3 ]
Chen, Wei [1 ,3 ]
Liu, Ai-Lin [1 ,3 ]
Chen, Yuan-Zhong [2 ]
Lin, Xin-Hua [1 ,3 ]
机构
[1] Fujian Med Univ, Fac Pharm, Dept Pharmaceut Anal, Fuzhou 350004, Peoples R China
[2] Fujian Med Univ, Affiliated Union Hosp, Fujian Inst Hematol, Fujian Key Lab Hematol, Fuzhou 350000, Peoples R China
[3] Fujian Med Univ, Nano Med Technol Res Inst, Fuzhou 350004, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Label-free electrochemical DNA biosensor; Multidrug resistance gene; Au nanoparticles/toluidine blue-graphene oxide nanocomposites; GRAPHITE OXIDE; P-GLYCOPROTEIN; IMMUNOSENSOR; ELECTRODE; SENSOR; FILM; FUNCTIONALIZATION; IMMUNOASSAY; EXPRESSION; REDUCTION;
D O I
10.1016/j.snb.2014.10.059
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The occurrence of multidrug resistance (MDR) has become a major obstacle to the successful performance of chemotherapy for cancer patients, so it is highly required to develop methods to explore the new strategy to early diagnose the MDR. Here, we report a novel label-free electrochemical DNA biosensor for simple, effective and convenient determination of MDR1 gene based on Au nanoparticles/toluidine blue-graphene oxide (Au NPs/TB-GO) modified electrode. The resulting Au NPs/TB-GO nanocomposites were characterized by scanning electron microscopy, atomic force microscope, ultraviolet-visible spectrometry, cyclic voltammetry, and electrochemical impedance spectroscopy. Differential pulse voltammetry was employed to monitor the hybridization of DNA by measuring the changes in the peak currents of TB. Under optimal conditions, the decreased currents were proportional to the logarithm of the concentration of the target DNA in the range of 1.0 x 10(-11)-1.0 x 10(-9) M with a detection limit of 2.95 x 10(-12) M (at an S/N of 3). In addition, the biosensor exhibited good selectivity, acceptable stability and reproducibility. The proposed method was simple, fast and inexpensive for the determination of MDR1 gene at low levels. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 276
页数:8
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