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MoS2 quantum dots as a unique fluorescent "turn-off-on" probe for the simple and rapid determination of adenosine triphosphate
被引:48
|作者:
Zhong, Yaping
[1
,2
]
Yi, Tao
[1
,2
]
机构:
[1] Fudan Univ, Dept Chem, 2005 Songhu Rd, Shanghai 200438, Peoples R China
[2] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, 2005 Songhu Rd, Shanghai 200438, Peoples R China
基金:
中国国家自然科学基金;
关键词:
RESONANCE ENERGY-TRANSFER;
CARBON DOTS;
ONE-POT;
ATP;
PHOTOLUMINESCENCE;
EVOLUTION;
FORSTER;
ELECTROCHEMILUMINESCENCE;
APTASENSOR;
FACILE;
D O I:
10.1039/c9tb00191c
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
We report a one-step hydrothermal method for the preparation of fluorescent molybdenum disulfide quantum dots (MoS2 QDs) and demonstrate the feasibility of fluorescent turn-off-on sensing of adenosine triphosphate (ATP) by using the MoS2 QDs. MoS2 QDs having strong blue-green fluorescence at 506 nm and good water-solubility were successfully synthesized by using ammonium tetrathiomolybdate as a single precursor. The fluorescence of MoS2 QDs was first quenched by Fe3+ through the formation of a MoS2 QDs/Fe3+ complex. ATP with the ability to coordinate with Fe3+ caused the dissociation of MoS2 QDs/Fe3+, resulting in the final release of MoS2 QDs and the recovery of fluorescence through a one-step competitive chelating process that took only 10 min to reach equilibrium at room temperature (RT). Facile and rapid sensing of Fe3+ and ATP could thus be achieved through the fluorescent turn-off-on strategy. Good linear relationships were obtained over the concentration ranges of 0-200 M for Fe3+ and 0-140 M for ATP with a lowest detectable concentration of 5 M for ATP. Satisfactory results were obtained when the method was applied to a standard addition recovery trial of ATP in human serum samples. No complex surface modification during the preparation or detection process was needed based on the fluorescent turn-off-on method of the MoS2 QDs, which suggests its great potential in fluorescent sensing.
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页码:2549 / 2556
页数:8
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