Fabrication by Laser Irradiation in a Continuous Flow Jet of Carbon Quantum Dots for Fluorescence Imaging

被引:93
作者
Donate-Buendia, Carlos [1 ]
Torres-Mendieta, Rafael [2 ]
Pyatenko, Alexander [3 ]
Falomir, Eva [4 ]
Fernandez-Alonso, Mercedes [1 ]
Minguez-Vega, Gladys [1 ]
机构
[1] Univ Jaume 1, GROC UJI, Inst New Imaging Technol, Avda Sos Baynat Sn, Castellon de La Plana 12071, Spain
[2] Tech Univ Liberec, Inst Nanomat Adv Technol & Innovat, Studentska 1402-2, Liberec 46117, Czech Republic
[3] Natl Inst Adv Ind Sci & Technol, Nanomat Res Inst, Tsukuba Cent 5,1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
[4] Univ Jaume 1, Dept Inorgan & Organ Chem, Avda Sos Baynat Sn, Castellon de La Plana 12071, Spain
关键词
COLLOIDAL NANOPARTICLES; NANODOTS SYNTHESIS; ABLATION; LIQUID; CELLS; PHOTOLUMINESCENCE; FRAGMENTATION; MECHANISM; GRAPHITE; TISSUES;
D O I
10.1021/acsomega.7b02082
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fluorescent carbon quantum dots (CQDs) are synthesized by laser irradiation of carbon glassy particles suspended in polyethylene glycol 200 by two methods, a batch and a flow jet configuration. The flow jet configuration is carried out by the simple combination of common laboratory objects to construct a home-made passage reactor of continuous flow. Despite the simplicity of the system, the laser energy is better harvested by the carbon microparticles, improving the fabrication efficiency a 15% and enhancing the fluorescence of CQDs by an order of magnitude in comparison with the conventional batch. The flow jet-synthesized CQDs have a mean size of 3 nm and are used for fluorescent imaging of transparent healthy and cancer epithelial human cells. Complete internalization is observed with a short incubation time of 10 min without using any extra additive or processing of the cell culture. The CQDs are well fixed in the organelles of the cell even after its death; hence, this is a simple manner to keep the cell information for prolonged periods of time. Moreover, the integrated photostability of the CQDs internalized in in vitro cells is measured and it remains almost constant during at least 2 h, revealing their outstanding performance as fluorescent labels.
引用
收藏
页码:2735 / 2742
页数:8
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