Poly(o-phenylenediamine)-carried nanogold particles as signal tags for sensitive electrochemical immunoassay of prolactin

被引:47
|
作者
Chen, Huafeng [1 ,2 ]
Cui, Yuling [1 ,2 ]
Zhang, Bing [1 ,2 ]
Liu, Bingqian [1 ,2 ]
Chen, Guonan [1 ,2 ]
Tang, Dianping [1 ,2 ]
机构
[1] Fuzhou Univ, Dept Chem, Key Lab Anal & Detect Food Safety, Minist Educ, Fuzhou 350108, Peoples R China
[2] Fuzhou Univ, Dept Chem, Fujian Prov Key Lab Anal & Detect Technol Food Sa, Fuzhou 350108, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Electrochemical immunoassay; Nanogold-assembled; poly(o-phenylenediamine) microspheres; Nanolabels; Prolactin; CARCINOEMBRYONIC ANTIGEN; GOLD NANOPARTICLES; AMPLIFICATION; IONS; DNA; TRANSDUCTION; ENHANCEMENT; POLYMERS;
D O I
10.1016/j.aca.2012.03.052
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel class of redox-active molecular tags, poly(o-phenylenediamine)-carried nanogold particles (GPPDs), was first synthesized and functionalized with horseradish peroxidase-anti-prolactin conjugates (HRP-anti-PRL). Thereafter, a specific sandwich-type electrochemical immunoassay was designed for determination of prolactin (PRL) by using GPPD-labeled HRP-anti-PRL conjugates as molecular tags on anti-PRL antibody-modified glassy carbon electrode. Compared with pure gold nanoparticles and poly(o-phenylenediamine) microspheres, the as-prepared GPPDs increased the surface coverage of the nanostructures, and enhanced the immobilization amount of biomolecules. Several labeling protocols compromising GPPD-labeled HRP-anti-PRL, nanogold particles-labeled HRP-anti-PRL and poly(o-phenylenediamine) microspheres-labeled HRP-anti-PRL, were investigated for detection of PRL, and improved analytical features were obtained with the GPPD-based strategy. With the GPPD labeling method, dependence of the electrochemical signals on the incubation time and pH of the assay solution were also studied. The strong attachment of HRP-anti-PRL to the GPPDs resulted in a good repeatability and intermediate reproducibility down to 9.8%. The dynamic concentration range spanned from 0.5 to 180 ng mL(-1) PRL with a detection limit of 0.1 ng mL(-1) at the 3S(blank) level. No significant differences at the 95% confidence level were encountered in the analysis of 10 spiked blank cattle serum samples between the developed immunoassay and enzyme-linked immunosorbent assay method for determination of PRL (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 25
页数:8
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