An efficient turn-on fluorescence biosensor for the detection of glutathione based on FRET between N,S dual-doped carbon dots and gold nanoparticles

被引:52
作者
Dong, Wenjuan [1 ,2 ]
Wa, Ruiping [1 ,2 ]
Gong, Xiaojuan [1 ,2 ]
Dong, Chuan [1 ,2 ]
机构
[1] Shanxi Univ, Inst Environm Sci, 92 Wu Cheng Rd, Taiyuan 030006, Shanxi, Peoples R China
[2] Shanxi Univ, Sch Chem & Chem Engn, 92 Wu Cheng Rd, Taiyuan 030006, Shanxi, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
N; S dual-doped carbon dots; Gold nanoparticles; Fluorescence resonance energy transfer; Glutathione; HIGHLY SELECTIVE DETECTION; QUANTUM DOTS; SENSING PLATFORM; PROBE; PEROXIDASE; CYSTEINE; SENSOR; ACID; RECOGNITION; ASSAY;
D O I
10.1007/s00216-019-02042-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence resonance energy transfer (FRET) is a kind of energy transfer mechanism depending on the distance between donor and acceptor, which exhibited potential application in biosensors. In this study, an efficient fluorescence "turn-on" strategy for the detection of glutathione (GSH) has been established based on FRET between nitrogen and sulfur dual-doped carbon dots (N,S-CDs) and gold nanoparticles (Au NPs). A novel N,S-CDs was synthesized by a one-pot hydrothermal treatment of 3-aminothiophenol, which possessed excellent fluorescence property with the maximum emission wavelength of 530 nm. Then, the as-prepared N,S-CDs served as energy donor to transfer energy to Au NPs via FRET process, resulting in fluorescence quenching of N,S-CDs. However, the fluorescence of N,S-CDs was recovered efficiently by adding GSH into the mixture solution of N,S-CDs and Au NPs. Therefore, the FRET assembly of N,S-CDs and Au NPs was used as a fluorescence probe for the "turn-on" sensing GSH with the linear range from 3.8 to 415.1 mu M and the limit detection of 0.21 mu M. This nanosensor platform was employed to monitor GSH in serum samples with satisfying results.
引用
收藏
页码:6687 / 6695
页数:9
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