Simultaneous detection of guanine, adenine, thymine and cytosine at choline monolayer supported multiwalled carbon nanotubes film

被引:90
作者
Wang, Po [1 ]
Wu, Hai [1 ]
Dai, Zong [1 ]
Zou, Xiaoyong [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
关键词
Purine; Pyrimidine; Electrocatalytic oxidation; Multiwalled carbon nanotubes; Choline; IONIC LIQUID ELECTRODE; ELECTROCHEMICAL DETECTION; AMPEROMETRIC DETERMINATION; BETA-CYCLODEXTRIN; DNA; CHROMATOGRAPHY; GRAPHITE; PURINE; NANOPARTICLES; NUCLEOTIDES;
D O I
10.1016/j.bios.2011.01.011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A rapid, convenient and accurate method for the simultaneous detection of guanine (G), adenine (A), thymine (T) and cytosine (C) was developed at a multiwalled carbon nanotube (MWCNT)/choline (Ch) monolayer-modified glassy carbon electrode (GCE). X-ray photoelectron spectroscopy data demonstrated that Ch was covalently immobilised on the surface of GCE through oxygen atom. The Ch monolayer provides a positively charged surface with -N+(CH3)(3) polar groups, so that it can attract negatively charged MWCNTs to the surface. Consequently, the MWCNT/Ch film exhibited remarkable electrocatalytic activities towards the oxidation of G, A, T and C due to the advantages of high electrode activity, large surface area, prominent antifouling property, and high electron transfer kinetics. All purine and pyrimidine bases showed well-defined catalytic oxidation peaks at MWCNT/Ch/GCE. The peak separations between G and A, A and T, and T and C are 270, 200, and 190 mV, respectively, which are sufficiently large for their potential recognition and simultaneous detection in mixture. Under the optimum conditions, the designed MWCNT/Ch/GCE exhibited low detection limit, high sensitivity and wide linear range for simultaneous detection of G, A, T and C. Moreover, the proposed method was successfully applied to the assessment of G, A, T and C contents in a herring sperm DNA sample with satisfactory results. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:3339 / 3345
页数:7
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