Li Kuen-Che, Huang Lynn L H, Liang Jhih-Hao, Chan Ming-Che
College of Photonics, National Chiao-Tung University, Taiwan; Equal contribution.
Department of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Taiwan; Institute of Biotechnology, National Cheng Kung University, Taiwan; Research Center of Excellence in Regenerative Medicine, National Cheng Kung University, Taiwan; Equal contribution.
Biomed Opt Express. 2016 Oct 31;7(11):4803-4815. doi: 10.1364/BOE.7.004803. eCollection 2016 Nov 1.
A simple approach to multi-color two-photon microscopy of the red, green, and blue fluorescent indicators was reported based on an ultra-compact 1.03-μm femtosecond laser and a nonlinear fiber. Inside the nonlinear fiber, the 1.03-μm laser pulses were simultaneously blue-shifted to 0.60.8 μm and red-shifted to 1.21.4 μm region by the Cherenkov radiation and fiber Raman gain effects. The wavelength-shifted 0.60.8 μm and 1.21.4 μm radiations were co-propagated with the residual non-converted 1.03-μm pulses inside the same nonlinear fiber to form a fiber-output three-color femtosecond source. The application of the multi-wavelength sources on multi-color two-photon fluorescence microscopy were also demonstrated. Overall, due to simple system configuration, convenient wavelength conversion, easy wavelength tunability within the entire 0.7~1.35 μm bio-penetration window and less requirement for high power and bulky light sources, the simple approach to multi-color two-photon microscopy could be widely applicable as an easily implemented and excellent research tool for future biomedical and possibly even clinical applications.
基于超紧凑型1.03μm飞秒激光器和非线性光纤,报道了一种用于红色、绿色和蓝色荧光指示剂的多色双光子显微镜的简单方法。在非线性光纤内部,1.03μm激光脉冲通过切伦科夫辐射和光纤拉曼增益效应同时蓝移至0.60.8μm并红移至1.21.4μm区域。波长移位后的0.60.8μm和1.21.4μm辐射与同一非线性光纤内残留的未转换1.03μm脉冲共同传播,形成光纤输出的三色飞秒光源。还展示了多波长光源在多色双光子荧光显微镜中的应用。总体而言,由于系统配置简单、波长转换方便、在整个0.7~1.35μm生物穿透窗口内易于波长调谐以及对高功率和笨重光源的要求较低,这种多色双光子显微镜的简单方法作为一种易于实施且出色的研究工具,可广泛应用于未来的生物医学甚至临床应用。