4.7 Article

A sensitive surface-enhanced Raman scattering enzyme-catalyzed immunoassay of respiratory syncytial virus

Journal

TALANTA
Volume 148, Issue -, Pages 308-312

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2015.10.081

Keywords

Enzyme-linked immunosorbent assay; Surface-enhanced Raman scattering; Respiratory syncytial virus; 3, 3 '-5, 5 '-Tetramethylbenzidine

Funding

  1. National Basic Research Program of China (973 Program) [2011CB933600]
  2. Fund of Chongqing Fundamental and Advanced Research Project [cstc2013jcyjA50008]
  3. Fundamental Research Funds for the Central Universities [XDJK2016C074]

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Respiratory viruses have become a major global health challenge which would benefit from advances in screening methods for early diagnosis. Respiratory syncytial virus (RSV) is one of the most important pathogen causing severe lower respiratory tract infections. Here we present a novel surface-enhanced Raman scattering (SERS) enzyme-catalyzed immunoassay of RSV by employing peroxidase substrate 3, 3'-5, 5'-tetramethylbenzidine (TMB) as Raman molecule. Horseradish peroxidase (HRP) attached to the detection antibody in a novel sandwich immunoassay catalyzes the oxidation of TMB by H2O2 to give a radical cation (TMB+), which could be easily adsorbed on the negatively charged surface of silver nanoparticles (AgNPs) through electrostatic interaction, inducing the aggregation of AgNPs and thus giving a strong SERS signal. A linear relationship was obtained between the Raman intensity and the amount of RSV in the range from 0.5 to 20 pg/mL, and the minimum detectable concentration of this SERS-based enzyme immunoassay was 0.05 pg/mL, which was 20 times lower than that found in the colorimetric method. (C) 2015 Elsevier B.V. All rights reserved.

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