4.7 Article

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

期刊

ANALYTICA CHIMICA ACTA
卷 728, 期 -, 页码 18-25

出版社

ELSEVIER
DOI: 10.1016/j.aca.2012.03.052

关键词

Electrochemical immunoassay; Nanogold-assembled; poly(o-phenylenediamine) microspheres; Nanolabels; Prolactin

资金

  1. Research Fund for the Doctoral Program of Higher Education of China [20103514120003]
  2. National Science Foundation of Fujian Province [2011J06003]
  3. National Natural Science Foundation of China [21075019, 41176079]
  4. 973 National Basic Research Program of China [2010CB732403]
  5. Program for Changjiang Scholars and Innovative Research Team in University [IRT1116]

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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.

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