Electrochemiluminescence Immunosensor Based on Au Nanocluster and Hybridization Chain Reaction Signal Amplification for Ultrasensitive Detection of Cardiac Troponin I

被引:60
作者
Zhu, Liping [1 ]
Ye, Jing [1 ]
Yan, Mengxia [1 ,2 ]
Zhu, Qiuju [1 ]
Wang, Shuang [1 ,2 ]
Huang, Jianshe [2 ]
Yang, Xiurong [1 ,2 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Cardiac troponin I; Electrochemiluminescence; Hybridization chain reaction; Au nanoclusters; Immunosensor; RESONANCE ENERGY-TRANSFER; GOLD NANOPARTICLES; ELECTROGENERATED CHEMILUMINESCENCE; AMPLIFIED ELECTROCHEMILUMINESCENCE; DNA; ASSAY; ACID; APTASENSOR; FRAMEWORKS; BIOSENSOR;
D O I
10.1021/acssensors.9b01369
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Measurement of cardiac troponin I in the blood is crucial for the early diagnosis of acute myocardial infarction. Herein, a novel and ultrasensitive electrochemiluminescence (ECL) immunosensor has been developed for determination of cardiac troponin I (cTnI) by using Au nanoclusters and hybridization chain reaction (HCR) signal amplification. In this ECL immunosensor, Au nanoclusters were dual-labeled at each end of hairpin DNA (H-1 and H-2) and acted as the luminophore. DNA initiator strands (T-1) and secondary antibody (Ab(2)) were conjugated on Au nano particles (AuNPs) to obtain a smart probe (Ab(2)-AuNP-T-1). In the presence of target cTnI, the sandwiched immunocomplex composed of cTnI, Ab(1), and Ab(2)-AuNP-T-1 was formed. Then the initiator strands T-1 of Ab(2)-AuNP-T-1 opened the hairpin DNA structures and triggered a cascade of hybridization events. Consequently, a large number of Au NCs were indirectly modified on the surface of the electrode, which could react with the coreactant (K2S2O8) and emit a strong ECL signal. Under the optimal conditions, the immunosensor exhibited a wide detection range for cTnI from 5 fg/mL to 50 ng/mL and a low detection limit of 1.01 fg/mL (S/N = 3). Because of the excellent specificity, stability, and reproducibility of the proposed ECL-HCR sensor, it has a great application prospect for cTnI detection in clinical diagnosis.
引用
收藏
页码:2778 / 2785
页数:15
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