TY - JOUR
T1 - Simple approach to three-color two-photon microscopy by a fiber-optic wavelength convertor
AU - Li, Kuen Che
AU - Huang, Lynn L.H.
AU - Liang, Jhih Hao
AU - Chan, Ming-Che
N1 - Publisher Copyright:
© 2016 Optical Society of America.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - 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 biopenetration 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.
AB - 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 biopenetration 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.
KW - Fluorescence microscopy
KW - Multispectral and hyperspectral imaging
KW - Nonlinear microscopy
KW - Nonlinear optics, fibers
KW - Ultrafast nonlinear optics
UR - http://www.scopus.com/inward/record.url?scp=84994517455&partnerID=8YFLogxK
U2 - 10.1364/BOE.7.004803
DO - 10.1364/BOE.7.004803
M3 - Article
AN - SCOPUS:84994517455
SN - 2156-7085
VL - 7
SP - 4803
EP - 4815
JO - Biomedical Optics Express
JF - Biomedical Optics Express
IS - 11
M1 - #274506
ER -