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Simple approach to three-color two-photon microscopy by a fiber-optic wavelength convertor

机译:光纤波长转换器对三色双光子显微镜的简单方法

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摘要

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 0.6~0.8 μm and red-shifted to 1.2~1.4 μm region by the Cherenkov radiation and fiber Raman gain effects. The wavelength-shifted 0.6~0.8 μm and 1.2~1.4 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.
机译:据报道,一种基于1.03μm超紧凑型飞秒激光和非线性光纤的红色,绿色和蓝色荧光指示剂的多色双光子显微术简单方法。在非线性光纤内部,由于切伦科夫辐射和光纤拉曼增益效应,1.03-μm激光脉冲同时蓝移至0.6〜0.8μm,红移至1.2〜1.4μm。将波长偏移的0.6〜0.8μm和1.2〜1.4μm的辐射与同一非线性光纤中残留的未转换的1.03 µm脉冲共同传播,以形成光纤输出的三色飞秒光源。还证明了多波长光源在多色双光子荧光显微镜上的应用。总的来说,由于简单的系统配置,方便的波长转换,在整个0.7〜1.35μm的生物渗透窗口范围内容易进行波长可调以及对大功率光源和大体积光源的需求较少,因此采用多色双光子显微镜的简单方法可能是作为未来生物医学乃至临床应用的一种易于实施且出色的研究工具,具有广泛的应用前景。

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