Correlative near-infrared light and cathodoluminescence microscopy using Y2O3:Ln, Yb (Ln = Tm, Er) nanophosphors for multiscale, multicolour bioimaging

被引:31
|
作者
Fukushima, S. [1 ]
Furukawa, T. [2 ]
Niioka, H. [1 ]
Ichimiya, M. [1 ,3 ]
Sannomiya, T. [4 ]
Tanaka, N. [5 ]
Onoshima, D. [6 ,7 ]
Yukawa, H. [7 ,8 ]
Baba, Y. [6 ,7 ,8 ,9 ]
Ashida, M. [1 ]
Miyake, J. [1 ]
Araki, T. [1 ]
Hashimoto, M. [1 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, 1-3 Machikaneyama Cho, Toyonaka, Osaka 5608531, Japan
[2] Osaka Univ, Inst NanoSci Design, 1-3 Machikaneyama Cho, Toyonaka, Osaka 5608531, Japan
[3] Univ Shiga Prefecture, Sch Engn, 2500 Hassaka Cho, Hikone, Shiga 5228533, Japan
[4] Tokyo Inst Technol, Dept Innovat & Engn Mat, 4259 Nagatsuta, Yokohama, Kanagawa 2268503, Japan
[5] RIKEN, Quantitat Biol Ctr QBiC, 1-3 Yamadaoka, Suita, Osaka 5650874, Japan
[6] Nagoya Univ, Inst Innovat Future Soc, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
[7] ImPACT Res Ctr Adv Nanobiodevices, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
[8] Nagoya Univ, Grad Sch Engn, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648603, Japan
[9] Natl Inst Adv Ind Sci & Technol, Hlth Res Inst, 2217-14 Hayashi Cho, Takamatsu, Kagawa 7610395, Japan
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
日本学术振兴会;
关键词
SCANNING-ELECTRON-MICROSCOPY; QUANTUM DOTS; CELL SHEETS; LUMINESCENCE; BEAM; EXCITATION; PROTEINS; TOOL;
D O I
10.1038/srep25950
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This paper presents a new correlative bioimaging technique using Y2O3:Tm, Yb and Y2O3:Er, Yb nanophosphors (NPs) as imaging probes that emit luminescence excited by both near-infrared (NIR) light and an electron beam. Under 980 nm NIR light irradiation, the Y2O3:Tm, Yb and Y2O3:Er, Yb NPs emitted NIR luminescence (NIRL) around 810 nm and 1530 nm, respectively, and cathodoluminescence at 455 nm and 660 nm under excitation of accelerated electrons, respectively. Multimodalities of the NPs were confirmed in correlative NIRL/CL imaging and their locations were visualized at the same observation area in both NIRL and CL images. Using CL microscopy, the NPs were visualized at the single-particle level and with multicolour. Multiscale NIRL/CL bioimaging was demonstrated through in vivo and in vitro NIRL deep-tissue observations, cellular NIRL imaging, and high-spatial resolution CL imaging of the NPs inside cells. The location of a cell sheet transplanted onto the back muscle fascia of a hairy rat was visualized through NIRL imaging of the Y2O3:Er, Yb NPs. Accurate positions of cells through the thickness (1.5 mm) of a tissue phantom were detected by NIRL from the Y2O3:Tm, Yb NPs. Further, locations of the two types of NPs inside cells were observed using CL microscopy.
引用
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页数:11
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