An "on-off-on" fluorescent nanoprobe for recognition of Cu2+ and GSH based on nitrogen co-doped carbon quantum dots, and its logic gate operation

被引:21
作者
Gao, Yifang [1 ]
Zhang, Huilin [1 ]
Shuang, Shaomin [1 ]
Han, Hui [1 ]
Dong, Chuan [1 ]
机构
[1] Shanxi Univ, Dept Inst Environm Sci, Sch Chem & Chem Engn, Taiyuan 030006, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
ENHANCED FLUORESCENCE; FLUOROMETRIC ANALYSIS; SILVER NANOCLUSTERS; RAPID DETECTION; GLUTATHIONE; COPPER; PROBE; IONS; SENSOR; NANOCOMPOSITES;
D O I
10.1039/c9ay00424f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Novel nitrogen co-doped carbon dots (NCDs) were synthesized as a fluorescent "on-off-on" switch for the highly sensitive and selective sensing of Cu2+ and glutathione (GSH) by a straightforward pyrolysis route. The as-prepared NCDs exhibited not only high optical stability but also superior biocompatibility and biolabeling potentials. The "on-off" process was realized by the introduction of Cu2+ on luminescent NCDs, which formed an NCDs-Cu2+ complex and quenched the fluorescence of NCDs efficiently. "Off-on" was also recovered upon addition of GSH owing to the competitive binding of GSH and Cu2+ leading Cu2+ to escape from the surface of the NCDs. The probe demonstrated high sensitivity and selectivity toward Cu2+ and GSH over other analytes, with a low detection limit of 3.62 x 10(-4) mu M and 6.32 x 10(-4) mu M, respectively. Concurrently, an "AND" logic gate was constructed based on the as-fabricated NCDs. Thanks to the highly intense emission of NCDs, the gradual quenching and restoration of their fluorescence with the addition of Cu2+ and further GSH could also be observed with the naked eye. More importantly, the probe was also extended to cellular imaging. The probe demonstrates high selectivity, repeatability, and stability, which offers a promising platform for environmental and biological sensing applications.
引用
收藏
页码:2650 / 2657
页数:8
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