Deep-tissue two-photon microscopy with a frequency-doubled all-fiber mode-locked laser at 937 nm

被引:13
|
作者
He, Hongsen [1 ]
Tang, Huajun [1 ]
Zhou, Meng [1 ]
Lai, Hei Ming [2 ,3 ,4 ]
Qiao, Tian [1 ]
Ren, Yu-xuan [5 ]
Lai, Cora S. W. [6 ,7 ]
Ko, Ho [2 ,3 ,4 ]
Wei, Xiaoming [8 ]
Yang, Zhongmin [8 ]
Tsia, Kevin K. [1 ,9 ]
Wong, Kenneth K. Y. [1 ,9 ]
机构
[1] Univ Hong Kong, Dept Elect & Elect Engn, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Fac Med, Dept Med & Therapeut, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Prince Wales Hosp, Li Ka Shing Inst Hlth Sci, Hong Kong, Peoples R China
[5] Fudan Univ, Inst Translat Brain Res, Shanghai Med Coll, Shanghai, Peoples R China
[6] Univ Hong Kong, Li Ka Shing Fac Med, Sch Biomed Sci, Hong Kong, Peoples R China
[7] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Hong Kong, Peoples R China
[8] South China Univ Technol, Sch Phys & Optoelect, Guangzhou, Peoples R China
[9] Adv Biomed Instrumentat Ctr, Hong Kong, Peoples R China
来源
ADVANCED PHOTONICS NEXUS | 2022年 / 1卷 / 02期
关键词
1.8 mu m laser; low repetition rate; high signal-to-noise ratio; mouse brain; fluorescence and second-harmonic-generation imaging; FLUORESCENCE; SPEED;
D O I
10.1117/1.APN.1.2.026001
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
In two-photon microscopy, low illumination powers on samples and a high signal-to-noise ratio (SNR) of the excitation laser are highly desired for alleviating the problems of photobleaching and phototoxicity, as well as providing clean backgrounds for images. However, the high-repetition-rate Ti:sapphire laser and the low-SNR Raman-shift lasers fall short of meeting these demands, especially when used for deep penetrations. Here, we demonstrate a 937-nm laser frequency-doubled from an all-fiber mode-locked laser at 1.8 mu m with a low repetition rate of similar to 9 MHz and a high SNR of 74 dB. We showcase two-photon excitations with low illumination powers on multiple types of biological tissues, including fluorescence imaging of mouse brain neurons labeled with green and yellow fluorescence proteins (GFP and YFP), DiI-stained and GFP-labeled blood vessels, Alexa Fluor 488/568-stained mouse kidney, and second-harmonic-generation imaging of the mouse skull, leg, and tail. We achieve a penetration depth in mouse brain tissues up to 620 mu m with an illumination power as low as similar to 10 mW, and, even for the DiI dye with an extremely low excitation efficiency of 3.3%, the penetration depth is still up to 530 mu m, indicating that the low-repetition-rate source works efficiently for a wide range of dyes with a fixed excitation wavelength. The low-repetition-rate and high-SNR excitation source holds great potential for biological investigations, such as in vivo deep-tissue imaging.
引用
收藏
页数:10
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