标题:In situ assembly of porous Au-paper electrode and functionalization of magnetic silica nanoparticles with HRP via click chemistry for Microcystin-LR immunoassay
作者:Ge, Shenguang; Liu, Weiyan; Ge, Lei; Yan, Mei; Yan, Jixian; Huang, Jiadong; Yu, Jinghua
作者机构:[Ge, Shenguang; Liu, Weiyan; Yan, Mei; Yan, Jixian; Huang, Jiadong; Yu, Jinghua] Univ Jinan, Shandong Univ, Key Lab Chem Sensing & Anal, Sch Chem & Ch 更多
通讯作者:Yu, J
通讯作者地址:[Yu, JH]Univ Jinan, Shandong Univ, Key Lab Chem Sensing & Anal, Sch Chem & Chem Engn, Jinan 250022, Peoples R China.
来源:BIOSENSORS & BIOELECTRONICS
出版年:2013
卷:49
页码:111-117
DOI:10.1016/j.bios.2013.05.010
关键词:Microcystin-LR; Click chemistry; Electrochemistry; Immunoassay
摘要: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.
收录类别:EI;SCIE
WOS核心被引频次:38
资源类型:期刊论文
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