A dual amplification strategy for ultrasensitive electrochemiluminescence immunoassay based on a Pt nanoparticles dotted graphene-carbon nanotubes composite and carbon dots functionalized mesoporous Pt/Fe

被引:23
作者
Deng, Wenping [1 ]
Liu, Fang [1 ]
Ge, Shenguang [2 ]
Yu, Jinghua [1 ]
Yan, Mei [1 ]
Song, Xianrang [3 ]
机构
[1] Univ Jinan, Key Lab Chem Sensing & Anal, Sch Chem & Chem Engn, Shandong Univ, Jinan 250022, Peoples R China
[2] Univ Jinan, Shandong Prov Key Lab Preparat & Measurement Bldg, Jinan 250022, Peoples R China
[3] Shandong Tumor Hosp, Canc Res Ctr, Jinan 250012, Peoples R China
基金
中国国家自然科学基金;
关键词
AMPLIFIED ELECTROCHEMICAL IMMUNOASSAY; CARCINOEMBRYONIC ANTIGEN; SENSITIVE IMMUNOSENSOR; MULTIPLEXED DETECTION; DNA HYBRIDIZATION; TRANSDUCTION; ELECTRODES; PROTEINS; AU;
D O I
10.1039/c3an02084c
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A facile and sensitive electrochemiluminescence (ECL) immunosensor for the detection of human carcinoembryonic antigen (CEA) was designed. The immunosensor used Pt nanoparticles dotted graphene-carbon nanotubes composites (Pt/Gr-CNTs) as a platform and carbon dots functionalized Pt/Fe nanoparticles (Pt/Fe@CDs) as bionanolabels. The Pt/Gr-CNTs was first synthesized using a facile ultrasonic method to modify the working electrode, which increases the surface area to capture a large amount of primary anti-CEA antibodies as well as improving the electronic transmission rate. The bionanolabels Pt/Fe@CDs prepared through ethanediamine linking, showed good ECL signal amplification performance. The reason is that the Pt/Fe@CDs nanocomposites as signal tags can increase CDs loading per immunoreaction in comparison with single CDs. The approach provided a good linear response range from 0.003 to 600 ng mL(-1) with a low detection limit of 0.8 pg mL(-1). The immunosensor showed good specificity, acceptable stability and reproducibility. Satisfactory results were obtained in the determination of CEA in human serum albumin samples. Hence, the proposed ECL immunosensor could become a promising method for tumor marker detection.
引用
收藏
页码:1713 / 1720
页数:8
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