Er3+ -Doped Y2O3 Nanophosphors for Near-Infrared Fluorescence Bioimaging Applications

被引:44
|
作者
Venkatachalam, Nallusamy [1 ]
Yamano, Tomoyoshi [2 ]
Hemmer, Eva [1 ]
Hyodo, Hiroshi [1 ,3 ]
Kishimoto, Hidehiro [1 ,2 ]
Soga, Kohei [1 ,3 ]
机构
[1] Tokyo Univ Sci, Res Inst Sci & Technol, Ctr Technol Canc, Noda, Chiba 2780022, Japan
[2] Tokyo Univ Sci, Res Inst Biomed Sci, Div Immunobiol, Noda, Chiba 2780022, Japan
[3] Tokyo Univ Sci, Dept Mat Sci & Technol, Tokyo 1258585, Japan
关键词
UP-CONVERSION; IN-VIVO; CERAMIC NANOPHOSPHORS; NANOPARTICLES; NANOSTRUCTURES;
D O I
10.1111/jace.12476
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Rare-earth-doped ceramic nanophosphor (RED-CNP) materials are promising near-infrared (NIR) fluorescence bioimaging (FBI) agents that can overcome problems of currently used organic dyes including photobleaching, phototoxicity, and light scattering. Here, we report a NIR-NIR bioimaging system by using NIR emission at 1550nm under 980nm excitation which can allow a deeper penetration depth into biological tissues than ultraviolet or visible light excitation. In this study, erbium-doped yttrium oxide nanoparticles (Er3+:Y2O3) with an average particle size of 100 and 500nm were synthesized by surfactant-assisted homogeneous precipitation method. NIR emission properties of Er3+:Y2O3 were investigated under 980nm excitation. The surface of Er3+:Y2O3 was electrostatically PEGylated using poly (ethylene glycol)-b-poly(acrylic acid) (PEG-b-PAAc) block copolymer to improve the chemical durability and dispersion stability of Er3+:Y2O3 under physiological conditions. In vitro cytotoxic effects of bare and PEG-b-PAAc-modified Er3+:Y2O3 were investigated by incubation with mouse macrophage cells (J774). Microscopic and macroscopic FBI were demonstrated in vivo by injection of bare or PEG-b-PAAc-modified Er3+:Y2O3 into C57BL/6 mice. The NIR fluorescence images showed that PEG-b-PAAc modification significantly reduced the agglomeration of Er3+:Y2O3 in mice and enhanced the distribution of Er3+:Y2O3.
引用
收藏
页码:2759 / 2765
页数:7
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