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Visible continuum pulses based on enhanced dispersive wave generation for endogenous fluorescence imaging
Quan Cui1,2, Zhongyun Chen1,2, Qian Liu1,2
1Collaborative Innovation Center for Biomedical Engineering, Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.
Biomedical Optics Express
|October 3, 2017
Summary
We generated broadband visible continuum pulses for advanced imaging. This technique enables simultaneous NADH and tryptophan imaging in mouse tissues using nonlinear microscopy.
Area of Science:
- Optics and Photonics
- Biomedical Imaging
- Laser Physics
Background:
- Nonlinear microscopy often relies on specific laser wavelengths.
- Ti:sapphire oscillators typically operate in the near-infrared, limiting visible-light applications.
- Endogenous fluorescence imaging requires efficient excitation sources.
Purpose of the Study:
- To generate broadband visible continuum pulses for nonlinear microscopy.
- To enable simultaneous imaging of NADH and tryptophan in biological tissues.
- To extend the accessible wavelength range for nonlinear microscopy.
Main Methods:
- Utilized a 100-fs Ti:sapphire oscillator and nonlinear photonic crystal fiber.
- Employed enhanced dispersive wave generation in the anomalous dispersion region.
- Optimized fiber length to minimize continuum pulse width.
- Generated broadband (500-700 nm) high-power (150 mW) continuum pulses.
Main Results:
- Successfully generated broadband visible continuum pulses (500-700 nm).
- Achieved simultaneous two-photon microscopy imaging of NADH and tryptophan in mice tissues.
- Demonstrated the utility of generated pulses for visible-wavelength nonlinear microscopy.
Conclusions:
- The developed method extends nonlinear microscopy to the visible wavelength range.
- This technique is valuable for applications requiring visible laser pulses, overcoming limitations of traditional Ti:sapphire oscillators.
- Enables advanced endogenous fluorescence imaging of biological samples.

