Design an aptasensor based on structure-switching aptamer on dendritic gold nanostructures/Fe3O4@SiO2/DABCO modified screen printed electrode for highly selective detection of epirubicin

被引:61
作者
Hashkavayi, Ayemeh Bagheri [1 ]
Raoof, Jahan Bakhsh [1 ]
机构
[1] Univ Mazandaran, Fac Chem, Dept Analyt Chem, Electroanalyt Chem Res Lab, Babol Sar, Iran
基金
美国国家科学基金会;
关键词
Aptamer; Epirubicin; Dendritic gold nanostructure; Carbon screen-printed electrode; DIRECT ELECTROCHEMISTRY; IONIC LIQUIDS; CARBON; HEMOGLOBIN; SENSOR; NANOPARTICLES; QUANTITATION; THROMBIN; ACID;
D O I
10.1016/j.bios.2017.01.025
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The present work describes a label free electrochemical aptasensor for selective detection of epirubicin. In this project, 5 '-thiole terminated aptamer was self-assembled on carbon screen printed electrode, which modified with electrodeposited gold nanoparticles on magnetic double-charged diazoniabicyclo [2.2.2] octane dichloride silica hybrid (Fe3O4@SiO2/DABCO) by Au-S bond. The interactions of epirubicin with aptamer on the AuNPs/Fe3O4@SiO2/DABCO/SPE have been studied by cyclic voltammetry, linear sweep voltammetry and electrochemical impedance spectroscopy. Under optimized conditions, the peak current of epirubicin increased linearly with increasing epirubicin concentration, due to the switching in the aptamer conformation and formation of aptamer-epirubicin complex instead of aptamer on the modified electrode surface. The Apt/AuNPs/Fe3O4@SiO2/DABCO/SPE is sensitive, selective and has two linear range from 0.07 mu M to 1.0 mu M and 1.0 mu M to 21.0 mu M with a detection limit of 0.04 mu M. The applicability of the aptasensor was successfully assessed by determination of epirubicin in a human blood serum sample.
引用
收藏
页码:650 / 657
页数:8
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