Quinoline derivative-functionalized carbon dots as a fluorescent nanosensor for sensing and intracellular imaging of Zn2+

被引:137
作者
Zhang, Zhaomin [1 ]
Shi, Yupeng [1 ]
Pan, Yi [1 ]
Cheng, Xin [1 ]
Zhang, Lulu [1 ]
Chen, Junying [1 ]
Li, Mei-Jin [2 ]
Yi, Changqing [1 ]
机构
[1] Sun Yat Sen Univ, Sch Engn, Key Lab Sensing Technol & Biomed Instruments Guan, Guangzhou 510275, Guangdong, Peoples R China
[2] Fuzhou Univ, Dept Chem, Minist Educ & Fujian Prov, Key Lab Anal & Detect Technol Food Safety, Fuzhou 350002, Peoples R China
关键词
RESONANCE ENERGY-TRANSFER; ONE-POT SYNTHESIS; QUANTUM DOTS; ZINC IONS; IN-VIVO; RHODAMINE SPIROLACTAM; COPPER IONS; PROBE; SENSOR; NANOPARTICLES;
D O I
10.1039/c4tb00677a
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
Surface functionalization of nanomaterials with highly specific recognition elements, such as biomolecules and organic molecules, has made possible many novel nanosensors for bio/chemical analysis and target bioimaging. In this report, a fluorescent nanosensor which exhibits highly specific recognition capability towards Zn2+ over competing metal ions has been developed through covalently functionalizing carbon dots (C-dots) with the quinoline derivatives which show response to Zn2+. The nanosensor exhibits excellent water solubility, biocompatibility, and cell-membrane permeability, and demonstrates high selectivity towards Zn2+ with a detection limit as low as 6.4 nM. Additionally, the rapid response of the nanosensor towards Zn2+ can be achieved within 1 min. The large amount of recognition units on the outer surface of an individual nanoparticle enables the signal amplification, hence making the immediate and highly sensitive detection of Zn2+ possible. Therefore, a reliable and highly specific nanosensor has been demonstrated for both rapid quantitative detection of Zn2+ in aqueous solution and real-time imaging of intracellular Zn2+, suggesting its potential and significance in bioanalysis and biomedical detection in the future.
引用
收藏
页码:5020 / 5027
页数:8
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