Ultrasensitive electrochemiluminescence detection of lengthy DNA molecules based on dual signal amplification

被引:10
|
作者
Liu, Fang [1 ]
Liu, Heng [2 ]
Zhang, Meng [1 ]
Yu, Jinghua [1 ]
Wang, Shaowei [1 ]
Lu, Juanjuan [1 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Key Lab Chem Sensing & Anal Univ Shandong, Jinan 250022, Peoples R China
[2] Shandong Univ, Qilu Hosp, Minist Hlth, Key Lab Otolaryngol, Jinan 250012, Peoples R China
关键词
NANOPOROUS GOLD ELECTRODE; ELECTROGENERATED CHEMILUMINESCENCE; CARBON NANOTUBES; GRAPHENE SHEETS; QUANTUM DOTS; BIOSENSOR; IMMUNOSENSOR; FILM; TRANSDUCTION; COMPOSITES;
D O I
10.1039/c3an00452j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Aimed at the facile detection of lengthy DNA molecules, an easily operated sandwich-type electrochemiluminescence (ECL) DNA biosensor was constructed on a glassy carbon electrode (GCE) based on CdTe quantum dots coated hollow ZnO nanoparticles (CdTe-ZnO NPs)-S2O82- ECL system in this work. To fabricate a high-performance protocol, the GCE surface was successively modified by graphene nanosheet (GS), carbon nanotube (CNT) and gold nanoparticles (AuNPs) to form AuNPs dotted CNT-GS composites (Au@CNT-GS) platform, which improved the electronic transmission rate as well as increased the amount of immobilized capture probe CMV-F (S-1). For further ultrasensitive, stable and low-potential ECL detection, CdTe-ZnO NPs were synthesized, and employed to label signal probe T7 promoter (S-3). Based on the hybridization effect, the immobilized capture probe S-1, target DNA and labeled signal probe S3 formed a sandwich-type DNA complex, which produced the ECL emission in the presence with S2O82- coreactant. Under optimal conditions, the DNA ECL biosensor showed a good linear range over 10(-14) M to 10(-19) M with a low detection limit of 0.61 x 10(-19) M. The proposed strategy demonstrates a reproducible, stable, and potent method that can be expanded to detect the genome which exists in living cells.
引用
收藏
页码:3463 / 3469
页数:7
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