Electrooxidation of DNA at glassy carbon electrodes modified with multiwall carbon nanotubes dispersed in polyethylenimine

被引:25
|
作者
Luque, Guillermina L. [1 ,4 ]
Ferreyra, Nancy F. [1 ]
Granero, Adrian [1 ,2 ]
Bollo, Soledad [3 ]
Rivas, Gustavo A. [1 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Quim Fis, INFIQC, RA-5000 Cordoba, Argentina
[2] Univ Nacl Rio Cuarto, Fac Ciencias Exactas & Nat, Dept Quim, Rio Cuarto, Argentina
[3] Univ Chile, Fac Ciencias Quim & Farrnaceut, Lab Bioelectroquim, Santiago, Chile
[4] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Matemat & Fis, INFIQC, RA-5000 Cordoba, Argentina
关键词
Polyethylenimine; DNA; Carbon nanotubes; Carbon nanotubes dispersion; DNA biosensor; ELECTROCHEMICAL SENSORS; LIGHT-SCATTERING; BIOSENSORS; IMMOBILIZATION; BIOMOLECULES;
D O I
10.1016/j.electacta.2011.07.036
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This work reports the electrochemical response of the complex between dsDNA and PEI formed in solution and at the surface of glassy carbon electrodes (GCE) modified with a dispersion of multi-walled carbon nanotubes in polyethylenimine (CNT-PEI). Scanning Electron Microscopy and Scanning Electrochemical Microscopy demonstrate that the dispersion covers the whole surface of the electrode although there are areas with higher density of CNT and, consequently, with higher electrochemical reactivity. The adsorption of DNA at GCE/CNT-PEI is fast and it is mainly driven by electrostatic forces. A clear oxidation signal is obtained either for dsDNA or a heterooligonucleotide of 21 bases (oligoY) at potentials smaller than those for the oxidation at bare GCE. The comparison of the behavior of DNA before and after thermal treatment demonstrated that the electrochemical response highly depends on the 3D structure of the nucleic acid. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9121 / 9126
页数:6
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