Multiplex electrochemiluminescence immunoassay of two tumor markers using multicolor quantum dots as labels and graphene as conducting bridge

被引:111
作者
Guo, Zhiyong [1 ]
Hao, Tingting [1 ]
Du, Shuping [1 ]
Chen, Beibei [1 ]
Wang, Zebo [1 ]
Li, Xing [1 ]
Wang, Sui [1 ]
机构
[1] Ningbo Univ, Fac Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Multiplex electrochemiluminescence immunoassay; Tumor markers; Quantum dots; Graphene; Chitosan; ELECTROCHEMICAL IMMUNOASSAY; IMMUNOSENSING SYSTEM; ALPHA-FETOPROTEIN; NANOPARTICLES; PLATFORM; CHANNEL; ANTIGEN; CANCER; CHIP;
D O I
10.1016/j.bios.2013.01.025
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A multiplex electrochemiluminescence (ECL) immunoassay for simultaneous determination of two different tumor markers, alpha-fetoprotein (AFP) and carcinoembryonic antigen (CEA), using multicolor quantum dots as labels and graphene as conducting bridge was developed. Herein, a typical sandwich immune complex was constructed on the glass carbon electrode, with QDs(525) and QDs(625) labeled on secondary anti-AFP and anti-CEA antibodies, respectively, thus to obtain distinguishable ECL signals. Because most of those QDs labeled on secondary antibodies were beyond the space domain of the ECL reaction, graphene was used as a conducting bridge to promote the electron transfer between QDs and the electrode, leading to about 30-fold enhancement of the ECL intensity. Experimental results revealed that the multiplex electrochemiluminescence immunoassay enabled the simultaneous monitoring of AFP and CEA in a single run with a working range of 0.001-0.1 pg/mL. The detection limit (LOD) for both analytes at 0.4 fg/mL was very low. No obvious cross-reactivity was found. Precision, recovery and stability were satisfactory. This novel multiplex ECL immunoassay provided a simple, sensitive, specific and reliable alternative for the simultaneous detection of tumor markers in clinical laboratory. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 107
页数:7
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