Synthesis and characterization of ZnS:Mn/ZnS core/shell nanoparticles for tumor targeting and imaging invivo

被引:17
|
作者
Yu, Zhangsen [1 ]
Ma, Xiying [2 ]
Yu, Bin [1 ]
Pan, Yuefang [1 ]
Liu, Zhaogang [1 ]
机构
[1] Shaoxing Univ, Sch Med, Shaoxing 312000, Peoples R China
[2] Suzhou Univ Sci & Technol, Sch Math & Phys, Suzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
ZnS:Mn; ZnS nanoparticles; fluorescence; tumor targeting and imaging; invivo; cytotoxicity; OPTICAL-PROPERTIES; QUANTUM DOTS; PHOTOLUMINESCENCE; NANOCRYSTALS; LUMINESCENCE; MN;
D O I
10.1177/0885328212444642
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Fluorescence imaging technique has been used for imaging of biological cells and tissues invivo. The Cd-free luminescent quantum dots conjugating with a cancer targeting ligand has been taken as a promising biocompatibility and low cytotoxicity system for targeted cancer imaging. This work reports the synthesis of fluorescent-doped core/shell quantum dots of water-soluble manganese-doped zinc sulfide. Quantum dots of manganese-doped zinc sulfide were prepared by nucleation doping strategy, with 3-mercaptopropionic acid as stabilizer at 90? in aqueous solution. The manganese-doped zinc sulfide nanoparticles exhibit strong orange fluorescence under UV irradiation, resistance to photo-bleaching, and low-cytotoxicity to HeLa cells. The structure and optical properties of nanoparticles were characterized by scanning electron microscope, X-ray diffraction, dynamic light scattering, and photoluminescence emission spectroscopy. Manganese-doped zinc sulfide nanoparticles conjugated with folic acid using 2,2-(ethylenedioxy)-bis-(ethylamine) as the linker. The covalent binding of both 2,2-(ethylenedioxy)-bis-(ethylamine) and folic acid on the surface of manganese-doped zinc sulfide nanoparticles probed by Fourier transform infrared spectroscopy detection. Furthermore, invitro cytotoxicity assessment of manganese-doped zinc sulfide-folic acid probes use HeLa cells. The obtained fluorescent probes (manganese-doped zinc sulfide) were used for tumor targeting and imaging invivo. The manganese-doped zinc sulfide-folic acid fluorescent probes which targeting the tumor cells in the body of nude mouse tumor model would emit orange fluorescence, when exposed to a 365nm lamp. We investigate the biodistribution of the manganese-doped zinc sulfide-folic acid fluorescent probes in tumor mouse model by measuring zinc concentration in tissues. These studies demonstrate the practicality of manganese-doped zinc sulfide-folic acid fluorescent probes as promising platform for tumor targeting and imaging invivo.
引用
收藏
页码:232 / 240
页数:9
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