4.7 Article

Irregular-shaped platinum nanoparticles as peroxidase mimics for highly efficient colorimetric immunoassay

Journal

ANALYTICA CHIMICA ACTA
Volume 776, Issue -, Pages 79-86

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2013.03.034

Keywords

Colorimetric immunoassay; Irregular-shaped platinum nanoparticles; Peroxidase mimics; Rabbit IgG

Funding

  1. National 973 Basic Research Program of China [2010CB732403]
  2. National Natural Science Foundation of China [41176079, 21075019]
  3. Doctoral Program of Higher Education of China [20103514120003]
  4. National Science Foundation of Fujian Province [2011J06003]
  5. China-Russia Bilateral Scientific Cooperation Research Program (NSFC/RFBR) [21211120157]
  6. Program for Changjiang Scholars and Innovative Research Team in University [IRT1116]

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Enzyme-linked immunosorbent assay (ELISA) methods based on natural enzyme-labeled probes have been applied in the immunoassays, but most have some inevitable limitations (e.g. harsh preparation, purification and storage) and are unsuitable for routine use. Herein we synthesized a new class of irregular-shaped platinum nanoparticles (ISPtNP) with a mean length of 7.0 nm and a narrowing width from 2.0 to 5.0 nm along the longitudinal axes, which were utilized as peroxidase-like mimics for the development of colorimetric immunoassays. Compared with bioactive horseradish peroxidase (HRP), the synthesized ISPtNP exhibited a low K-m value (similar to 0.12 mM) and a high K-cat value (similar to 2.27 x 10(4) s(-1)) for 3,3',5,5'-tetramethylbenzidine (TMB) with strong thermal stability and pH tolerance. The catalytic mechanism of the ISPtNP toward TMB/H2O2 was for the first time discussed and deliberated in this work. Based on a sandwich-type assay format, two types of colorimetric immunoassay protocols were designed and developed for the detection of rabbit IgG (RIgG, as a model) by using the synthesized ISPtNP and conventional HRP as the labeling of detection antibodies, respectively. Similar detection limits (LODs) of 2.5 ng mL(-1) vs. 1.0 ng mL(-1) were obtained toward RIgG with the ISPtNP labeling compared to HRP format. Intra- and inter-assay coefficients of variation were less than 13%. Importantly, the ISPtNP-based assay system could be suitable for use in a mass production of miniaturized lab-on-a-chip devices and open new opportunities for protein diagnostics and biosecurity. (C) 2013 Elsevier B.V. All rights reserved.

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