| Literature DB >> 27896017 |
Kuen-Che Li1, Lynn L H Huang2, Jhih-Hao Liang3, Ming-Che Chan4.
Abstract
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.Keywords: (060.4370) Nonlinear optics, fibers; (110.4234) Multispectral and hyperspectral imaging; (180.2520) Fluorescence microscopy; (180.4315) Nonlinear microscopy; (320.7110) Ultrafast nonlinear optics
Year: 2016 PMID: 27896017 PMCID: PMC5119617 DOI: 10.1364/BOE.7.004803
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732