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Thiol stabilized Au nanoclusters with efficient electrochemiluminescence for the simultaneous and ultrasensitive detection of GSH and Cu2+
被引:23
|作者:
Zhou, Ying
[1
,2
]
Shi, Xiaoyu
[2
]
Ma, Liang
[1
]
Chai, Yaqin
[2
]
Yuan, Ruo
[2
]
机构:
[1] Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
[2] Southwest Univ, Minist Educ, Coll Chem & Chem Engn, Key Lab Luminescence Anal & Mol Sensing, Chongqing 400715, Peoples R China
关键词:
Electrochemiluminescence;
Gold nanoclusters;
Thiol ligand;
Biosensor;
Glutathione;
Copper ions;
TURN-ON DETECTION;
ELECTROGENERATED CHEMILUMINESCENCE;
METALLIZATION;
NANOPARTICLES;
SYSTEM;
D O I:
10.1016/j.snb.2023.133518
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Herein, an electrochemiluminescence (ECL) biosensor was constructed for simultaneous and ultrasensitive detection of glutathione (GSH) and copper ion (Cu2+) due to thiol (captopril) stabilized gold nanoclusters (Au NCs) as a high-efficient ECL emitter. Impressively, we firstly demonstrated that thiol stabilized Au NCs (thiol-Au NCs) presented unexceptionable ECL performance over amino stabilized Au NCs (amino-Au NCs), due to fast electron transfer from massive Au-S electronic pathways in electrochemical excitation. Furthermore, GSH (target 1) and Cu2+ (target 2) could give rise to "on-off-on" ECL responses of Au NCs based on GSH-triggered competing reaction and Cu2+-specific-DNAzyme walker. As a result, the ECL biosensor achieved trace detection of GSH with a detection limit of 148 pM and Cu2+ with a detection limit of 91.5 fM. Thus, the strategy pointed out a definite direction to obtain ultra-bright ECL metal NCs for multiple biomarker testing, broadening the application in clinical diagnosis.
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页数:8
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