In Vivo Repeatedly Charging Near-Infrared-Emitting Mesoporous SiO2/ZnGa2O4:Cr3+ Persistent Luminescence Nanocomposites

被引:186
作者
Li, Zhanjun [1 ]
Zhang, Yuanwei [1 ]
Wu, Xiang
Wu, Xiaoqiong
Maudgal, Rohit [1 ]
Zhang, Hongwu [2 ]
Han, Gang [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Biol & Mol Pharmacol, Worcester, MA 01605 USA
[2] Chinese Acad Sci, Inst Urban Environm, Xiamen 361021, Peoples R China
基金
美国国家卫生研究院;
关键词
SILICA NANOSPHERES; UP-CONVERSION; TRAP DEPTH; NANOPARTICLES; FUNCTIONALIZATION; NANOPHOSPHORS; MECHANISM; AFTERGLOW;
D O I
10.1002/advs.201500001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Near-infrared (NIR) persistent phosphor ZnGa2O4:Cr3+ (ZGC) has unique deep-tissue rechargeable afterglow properties. However, the current synthesis leads to agglomerated products with irregular morphologies and wide size distributions. Herein, we report on in vivo rechargeable mesoporous SiO2/ZnGa2O4:Cr3+ (mZGC) afterglow NIR-emitting nanocomposites that are made by a simple, one-step mesoporous template method. At less than 600 degrees C, pores in mesoporous silica nanoparticles (MSNs) act as nanoreactors to generate in situ ZnGa2O4:Cr3+ NIR-persistent phosphors. The as-synthesized mZGC preserves defined size, morphology, and mesoporous nanostructure of the MSNs. The persistent luminescence of the as-synthesized mZGC is recharged in a simulated deep-tissue environment (e.g., similar to 8 mm pork slab) in vitro by using red light (620 nm). Moreover, mZGC can be repeatedly activated in vivo for persistent luminescence imaging in a live mouse model by using white LED as a light source. Our concept of utilizing mesoporous silica as nanoreactor to fabricate ZGC PL nanoparticles with controllable morphology and preserved porous nanostructure paves a new way to the development and the wide application of deep tissue rechargeable ZGC in photonics and biophotonics.
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页数:6
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