One- Pot Synthesis of Highly Luminescent Carbon Quantum Dots and Their Nontoxic Ingestion by Zebrafish for In Vivo Imaging

被引:77
作者
Huang, Yi-Fan [1 ,2 ]
Zhou, Xin [3 ]
Zhou, Rong [3 ]
Zhang, Hong [3 ]
Kang, Kai-Bin [2 ]
Zhao, Min [1 ]
Peng, Yong [4 ]
Wang, Qiang [1 ,2 ]
Zhang, Hao-Li [1 ]
Qiu, Wen-Yuan [2 ]
机构
[1] Lanzhou Univ, SKLAOC, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, Key Lab Nonferrous Met Chem & Resources Utilizat, Lanzhou 730000, Peoples R China
[3] Chinese Acad Sci, Inst Modern Phys, Lanzhou 730000, Peoples R China
[4] Lanzhou Univ, Sch Phys Sci & Technol, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
glycerol; green chemistry; in vivo imaging; quantum dots; zebrafish; DEPENDENT FLUORESCENCE; TRANSGENIC ZEBRAFISH; NANODOTS; NANOPARTICLES; GRAPHENE;
D O I
10.1002/chem.201400011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photoluminescent carbon and/or silicon-based nanodots have attracted ever increasing interest. Accordingly, a myriad of synthetic methodologies have been developed to fabricate them, which unfortunately, however, frequently involve relatively tedious steps, such as initial surface passivation and subsequent functionalization. Herein, we describe a green and sustainable synthetic strategy to combine these procedures into one step and to produce highly luminescent carbon quantum dots (CQDs), which can also be easily fabricated into flexible thin films with intense luminescence for future roll-to-roll manufacturing of optoelectronic devices. The as-synthesized CQDs exhibited enhanced cellular permeability and low or even noncytotoxicity for cellular applications, as corroborated by confocal fluorescence imaging of HeLa cells as well as cell viability measurements. Most strikingly, zebrafish were directly fed with CQDs for in vivo imaging, and mortality and morphologic analysis indicated ingestion of the CQDs posed no harm to the living organisms. Hence, the multifunctional CQDs potentially provide a rich pool of tools for optoelectronic and biomedical applications.
引用
收藏
页码:5640 / 5648
页数:9
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