Gold nanoparticles/L-cysteine/graphene composite based immobilization strategy for an electrochemical immunosensor

被引:33
作者
Wang, Guangfeng [1 ,2 ]
Huang, Hao [1 ,2 ]
Zhang, Ge [1 ,2 ]
Zhang, Xiaojun [1 ,2 ]
Fang, Bin [1 ,2 ]
Wang, Lun [1 ,2 ]
机构
[1] Anhui Normal Univ, Coll Chem & Mat Sci, Anhui Key Lab Funct Mol Solids, Anhui Key Lab Chem Biosensing, Wuhu 241000, Peoples R China
[2] Hefei Univ Technol, Anhui Key Lab Controllable Chem React & Mat Chem, Hefei 230009, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHENE SHEETS; HORSERADISH-PEROXIDASE; ANTIBODY IMMOBILIZATION; SURFACE; FILMS; OXIDE; AMPLIFICATION; NANOCOMPOSITES; CONSTRUCTION; IMMUNOASSAYS;
D O I
10.1039/c0ay00389a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel immobilization strategy combining gold nanoparticles (GNP) with graphene (Gr) via crosslinker L-cysteine (L-cys) for the enhancement of a HRP-labelled sandwiched electrochemical immunosensor was developed. In the fabrication process of the immobilization platform, graphene was first modified onto glassy carbon electrode (GCE), and then L-cys was electrodeposited onto the substrate of Gr for the following GNP assembling. The characteristics of the platform surface were studied by scanning electron microscopy (SEM), ultraviolet-visible (UV-vis) spectrometry, cyclic voltammetry (CV) and electrochemical alternating current impedance spectroscopy (EIS). From the SEM, interestingly we found the substrate of Gr induced the regular growth of L-cys, which may further improve the stable conjugation of GNP, which may result in more loading amount of the biomolecules. The special GNP/L-cys/Gr composite film constructed an effective antibody immobilization matrix and made the immunosensor hold high sensitivity, good stability and bioactivity. Under the optimized experimental conditions, a wide linear range of human IgG (HIgG) concentration from 0.2 to 320 ng mL(-1) and a detection limit of 70 ng mL(-1) were obtained. Accurate detection of HIgG in human serum samples was satisfyingly demonstrated by comparison to the standard ELISA assays.
引用
收藏
页码:1692 / 1697
页数:6
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