Amplified electrochemiluminescence detection of CEA based on magnetic Fe3O4@Au nanoparticles-assembled Ru@SiO2 nanocomposites combined with multiple cycling amplification strategy

被引:67
作者
Jie, Guifen [1 ]
Ge, Junjun [1 ]
Gao, Xiaoshan [1 ]
Li, Chunli [1 ]
机构
[1] Qingdao Univ Sci & Technol, Key Lab Analyt Chem Life Sci, Minist Educ,Coll Chem & Mol Engn,Univ Shandong, Key Lab Sensor Anal Tumor Marker,Shandong Key Lab, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemiluminescence; Ru@SiO2; Target recycling amplification; Fe3O4@Au; Quenching probe; ROLLING CIRCLE AMPLIFICATION; RESONANCE ENERGY-TRANSFER; GRAPHENE-QUANTUM DOTS; STRAND DISPLACEMENT AMPLIFICATION; ENZYMATIC SIGNAL AMPLIFICATION; HYBRIDIZATION CHAIN-REACTION; N-GLYCAN EXPRESSION; CARCINOEMBRYONIC ANTIGEN; SILICA NANOPARTICLES; ENHANCED ELECTROCHEMILUMINESCENCE;
D O I
10.1016/j.bios.2018.07.046
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, we designed a new strategy for ultrasensitive detection of CEA based on efficient electrochemiluminescence (ECL) quenching of Ru(bpy)(3)(2+)-doped SiO2 nanocomposite by ferrocene using target recycling amplification technique. A large number of Ru@SiO2 ECL signal probe were firstly assembled on the novel magnetic core - shell Fe3O4@Au nanoparticles (NPs), then the ferrocene-labeled ECL quenching probe (Fcprobe) was linked to the magnetic NPs. Finally, numerous DNA1 sequences were produced by target CEA-triggered multiple recycling amplification and displaced the Fc-probe on the magnetic NPs, leading to significantly enhanced ECL signal for CEA detection. Because of the designed cascade signal amplification strategy, the newly developed method achieved a wide linear range of 10 fg/mL to 10 ng/mL with a low detection limit of 3.5 fg/mL. Furthermore, taking advantages of the magnetic Fe3O4@Au NPs for caning abundant signal probes, sensing target and ECL detection, the developed ECL strategy is convenient, rapid and displayed high sensitivity for CEA detection, which has great potential for analyzing the clinical samples in practical disease diagnosis applications.
引用
收藏
页码:115 / 121
页数:7
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