A label-free electrochemical biosensor based on a DNA aptamer against codeine

被引:49
|
作者
Huang, Liangliang [1 ]
Yang, Xiaojuan [2 ]
Qi, Cui [2 ]
Niu, Xiaofang [1 ]
Zhao, Chunling [1 ]
Zhao, Xiaohui [1 ]
Shangguan, Dihua [2 ]
Yang, Yunhui [1 ]
机构
[1] Yunnan Normal Univ, Chem & Chem Engn Coll, Kunming 650092, Peoples R China
[2] Chinese Acad Sci, Key Lab Analyt Chem Living Biosyst, Inst Chem, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Codeine; Aptamer; Systematic evolution of ligands by exponential enrichment; Electrochemical aptasensor; Au-mesoporous silica nanoparticles; SELECTION; CHROMATOGRAPHY; RECOGNITION; APTASENSOR; MOLECULES; MORPHINE; URINE; CELLS; BIND;
D O I
10.1016/j.aca.2013.05.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In order to develop a sensor for opium alkaloid codeine detection, DNA aptamers against codeine were generated by SELEX (systematic evolution of ligands by exponential enrichment) technique. An aptamer HL7-14, which is a 37-mer sequence with K-d values of 0.91 mu M, was optimized by the truncation-mutation assay. The specificity investigation shows that HL7-14 exhibits high specificity to codeine over morphine, and almost cannot bind to other small molecule. With this new selected aptamer, a novel electrochemical label-free codeine aptamer biosensor based on Au-mesoporous silica nanoparticles (Au-MSN) as immobilized substrate has been proposed using [Fe(CN)(6)](3-/4-) as electroactive redox probe. The linear range covered from 10 pM to 100 nM with correlation coefficient of 0.9979 and the detection limit was 3 pM. Our study demonstrates that the biosensor has good specificity, stability and well regeneration. It can be used to detect codeine. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
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