4.8 Article

In situ assembly of porous Au-paper electrode and functionalization of magnetic silica nanoparticles with HRP via click chemistry for Microcystin-LR immunoassay

Journal

BIOSENSORS & BIOELECTRONICS
Volume 49, Issue -, Pages 111-117

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2013.05.010

Keywords

Microcystin-LR; Click chemistry; Electrochemistry; Immunoassay

Funding

  1. Natural Science Research Foundation of China [21207048, 21277058]
  2. Natural Science Foundation of Shandong Province, China [ZR2011BQ019, ZR2012BZ002]
  3. Technology Development Plan of Shandong Province, China [2011GGB01153, 2012GGB01181]
  4. State Key Laboratory of Environmental Chemistry and Ecotoxicology Research Center for Eco-Environmental Sciences Chinese Academy of Sciences [KF2011-03]

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A simple, low-cost and sensitive origami electrochemical immunoassay-device was developed based on a novel gold nanoparticle modified porous paper working electrode (Au-PWE) for point-of-care testing. Azide-functionalized Au-PWE was prepared by the functionalization of Au-PWE with 1-azidoundecan-11-thiol. Alkyne end-terminated antibody was prepared with 4-pentynoic acid and antibody by the 1-ethyl-3-(3-(dimethylamino) propyl) carbodiimide hydrochloride and N-hydroxysuccinimide activation reaction. Alkyne-antibody was coupled to azido-Au-PWE by click reaction as a recognition element. Nearly monodispersed sphere-like silica-coated ferroferric oxide (Fe3O4@SiO2) nanoparticles were prepared via the reverse microemulsion method. Azide-functionalized Fe3O4@SiO2 was prepared by the functionalization of silica shell with 3-bromopropyltrichlorosilane followed by substitution with sodium azide. Alkyne-functionalized antibody and horse radish peroxidase were coupled to azide-functionalized Fe3O4@SiO2 by click reaction as signal label. Horse radish peroxidase and ferroferric oxide could catalyze the oxidation of thionine in the presence of hydrogen peroxide. After the sandwich immunoreaction, the current was proportional to the logarithm of the Microcystin-LR. The linear regression equation was i(mu A)=119.89+46.27 log CMC-LR (mu g/mL) in the range from 0.01 to 200 mu g/mL The limit of detection was 0.004 mu g/mL This immunoassay would provide a universal immunoassay method in environmental monitoring and public health. (C) 2013 Elsevier B.V. All rights reserved.

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