Electrochemical immunosensor for carcinoembryonic antigen based on nanosilver-coated magnetic beads and gold-graphene nanolabels

被引:71
作者
Chen, Huafeng [1 ,2 ]
Tang, Dianping [1 ,2 ]
Zhang, Bing [1 ,2 ]
Liu, Bingqian [1 ,2 ]
Cui, Yuling [1 ,2 ]
Chen, Guonan [1 ,2 ]
机构
[1] Fuzhou Univ, Minist Educ, Key Lab Anal & Detect Food Safety, Dept Chem, Fuzhou 350108, Peoples R China
[2] Fuzhou Univ, Fujian Prov Key Lab Anal & Detect Technol Food Sa, Dept Chem, Fuzhou 350108, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金; 美国国家科学基金会;
关键词
Bionanolabels; Carcinoembryonic antigen; Electrochemical immunosensor; Nanogold-decorated graphene nanosheets; Redox-active magnetic nanostructures; SILVER NANOPARTICLES; POLY(O-PHENYLENEDIAMINE) FILM; CLINICAL IMMUNOASSAY; NANOCOMPOSITES; MICROPARTICLES; MEMBRANE; PLATFORM; LABELS;
D O I
10.1016/j.talanta.2012.01.025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel redox-active magnetic nanostructure was synthesized by using a wet chemical method for high-efficiency electrochemical immunoassay of carcinoembryonic antigen (CEA, as a model analyte). The nanostructures based on the combination of a magnetic nanocore, a layer of electroactive poly(o-phenylenediamine) (PPD), and a silver metallic shell displayed good adsorption properties for the attachment of anti-CEA antibody selective to CEA. The magnetic nanostructure presented good redox behaviors to facilitate and modulate the way it was integrated into a magnetic carbon paste electrode. The assay was based on a sandwich-type immunoassay protocol by using nanogold-patterned graphene oxide nanoscales (AuNP-GO), conjugated with horseradish peroxidase-labeled anti-CEA, as secondary antibodies and biofunctionalized magnetic nanostructures as immunosensing probes. Under optimal conditions, the nanoparticle-based immunocomposites exhibited good electrochemical responses for the determination of CEA, and allowed the detection of CEA at a concentration as low as 1.0 pg mL(-1) at a signal-to-noise ratio of 3. In addition, the magnetic immunosensing had good reproducibility, and acceptable accuracy, and could be successfully applied for the detection of CEA in the clinical serum specimens. Significantly, by controlling the target biomolecules, this assay can be easily extended for use with other immunosensings, and thus represents a versatile design routine. (C) 2012 Elsevier BM. All rights reserved.
引用
收藏
页码:95 / 102
页数:8
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