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Synthesis and cytotoxic effects of SrAl2O4 persistent luminescence nanoparticles co-doped with Eu2+/Dy3+ ions
被引:10
|作者:
Montes-Frausto, J. B.
[1
]
Juarez-Moreno, K.
[2
,3
]
Can-Uc, B.
[4
]
Hirata-Flores, G. A.
[2
]
机构:
[1] Ctr Invest Cient & Educ Super Ensenada, Posgrado Fis Mat, Apartado Postal 2732, Ensenada 22860, Baja California, Mexico
[2] Univ Nacl Autonoma Mexico, Ctr Nanociencias & Nanotecnol, Apartado Postal 14, Ensenada 22800, Baja California, Mexico
[3] CONACyT, Mexico City, DF, Mexico
[4] Ctr Invest Cient & Educ Super Ensenada, Dept Opt, Apartado Postal 2732, Ensenada 22860, Baja California, Mexico
来源:
关键词:
MECHANISM;
DY3+;
PHOTOLUMINESCENCE;
ALUMINATE;
AFTERGLOW;
EU2+;
D O I:
10.1364/OME.6.001488
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
Persistent luminescence strontium aluminate nanoparticles co-doped with Eu2+ and Dy3+ were prepared by urea-assisted combustion synthesis. Different percentages of co-dopants were evaluated in order to optimize luminescence of the nanophosphor. Luminescence measurements showed that excitation of this green-emitting phosphor occurred within a wide range of wavelengths (254 460 nm) while the half-life time of persistent luminescence laid within the seconds regime. Presence of Dy3+ as the co-dopant enhanced the green emission in this interval of time, and the entire decay time occurred in minutes. Crystallinity and morphology were evaluated by X-ray diffraction (XRD) and transmission electron microscopy (TEM), respectively. Strontium aluminate co-doped with 1% Eu, and 1% Dy, and 1% Eu, and 3% Dy emitted an intense green signal and long decay time. These crystal nanophosphors displayed sizes of 18 nm and 22 nm, respectively. The cytotoxic effect of nanoparticles was determined by a cell viability test where the tri-methyl-tetrazolium reagent (MTT) was reduced only by metabolically active cells. Different concentrations of bare nanoparticles were tested in a 96-well plate containing 10; 000 cells per well of a human cervix carcinoma cell line (HeLa). Evaluation of cell viability by this cytotoxic assay showed that in most of the cases cell viability was higher than 60% after incubation with bare nanoparticles. Since our bare nanoparticles were not cytotoxic, these results open a broad field of biomedical applications for phosphorescent materials as cell biolabels and imaging research area. (C) 2016 Optical Society of America
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页码:1488 / 1499
页数:12
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