An electrochemical stripping metalloimmunoassay based on silver-enhanced gold nanoparticle label

被引:152
作者
Chu, X
Fu, X
Chen, K
Shen, GL [1 ]
Yu, RQ
机构
[1] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Peoples R China
[2] Hunan Normal Univ, Chem & Chem Engn Coll, Key Lab Chem Biol & Trad Chinese Med Res, Minist Educ, Changsha 410081, Peoples R China
基金
中国国家自然科学基金;
关键词
gold nanoparticle; metalloimmunoassay; electrochemical stripping analysis; silver enhancement;
D O I
10.1016/j.bios.2004.07.012
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel, sensitive electrochemical immunoassay has been developed based on the precipitation of silver on colloidal gold labels which, after silver metal dissolution in an acidic solution, was indirectly determined by anodic stripping voltarmmetry (ASV) at a glassy-carbon electrode. The method was evaluated for a noncompetitive heterogeneous immunoassay of an immunoglobulin G (IgG) as a model. The influence of relevant experimental variables, including the reaction time of antigen with antibody, the dilution ratio of the colloidal gold-labeled antibody and the parameters of the anodic stripping operation, upon the peak current was examined and optimized. The anodic stripping peak current depended linearly on the IgG concentration over the range of 1.66 ng ml(-1) to 27.25 mug ml(-1) in a logarithmic plot. A detection limit as low as 1 ng ml(-1) (i.e., 6 x 10(-12) M) human IgG was achieved, which is competitive with colorimetric enzyme linked immuno-sorbent assay (ELISA) or with immunoassays based on fluorescent europium chelate labels. The high performance of the method is attributed to the sensitive ASV determination of silver (1) at a glassy-carbon electrode (detection limit of 5 x 10(-9) M) and to the catalytic precipitation of a large number of silver on the colloidal gold-labeled antibody. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1805 / 1812
页数:8
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