Electrochemical serotonin sensing interface based on double-layered membrane of reduced graphene oxide/polyaniline nanocomposites and molecularly imprinted polymers embedded with gold nanoparticles

被引:108
作者
Xue, Cheng [1 ]
Wang, Xi [1 ]
Zhu, Wanying [1 ]
Han, Qing [1 ]
Zhu, Chunhong [1 ]
Hong, Junli [1 ]
Zhou, Xuemin [1 ]
Jiang, Huijun [1 ]
机构
[1] Nanjing Med Univ, Sch Pharm, Nanjing 211166, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Serotonin; Functionalized gold nanoparticles; Embedded gold nanoparticles; Molecularly imprinted polymers; Electrochemical sensor; MODIFIED ELECTRODE; ASCORBIC-ACID; URIC-ACID; VOLTAMMETRIC SENSOR; CARBON; DOPAMINE; PLASMA; POLYANILINE; SURFACE; OXIDE;
D O I
10.1016/j.snb.2014.01.100
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A double-layered membrane sensing interface was fabricated for sensitive and selective detection of serotonin (5-hydroxytryptamine, 5-HT) based on reduced graphene oxide (rGO)/polyaniline (PANI) nanocomposites and molecularly imprinted polymers (MIPs) embedded with gold nanoparticles (AuNPs). rGO/PANI nanocomposites were synthesized via electro-deposition process, in which protonated ani-lines were first anchored on the rGO sheets through electrostatic adsorption, and then the rGO/PANI membrane was formed on the bare electrode via cyclic voltammetry method. Functionalized AuNPs (F-AuNPs) were prepared to fabricate the MIPs embedded with AuNPs (AuNPs@MIPs) membrane on the modified electrode by constant potential method in the presence of 5-HT and p-aminothiophenol. The materials prepared in this work were examined by ultraviolet-visible (UV-Vis) and Raman spectroscopy, and the as-prepared membranes were characterized by scanning electron microscope, energy dispersive spectroscopy, and electrochemical methods. In addition, the obtained sensor allowed remarkable selectivity to 5-HT against the interferences caused by ascorbic acid and other interferents. A linear dependence of peak current in differential pulse voltammograms was obtained over 0.2-10.0 mu mol L-1 5-HT with the limit of detection of 11.7 nmol L-1 (S/N = 3). Furthermore, the obtained biomimetic sensor was employed to detect 5-HT in human serum samples. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 63
页数:7
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