Fiber-based combined optical coherence and multiphoton endomicroscopy

被引:18
作者
Liu, Gangjun [1 ,2 ]
Chen, Zhongping [1 ,2 ]
机构
[1] Univ Calif Irvine, Beckman Laser Inst, Irvine, CA 92612 USA
[2] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
optical coherence microscopy; multiphoton microscopy; multimodal imaging; scanning microscopy; fiber device; MICROSCOPY;
D O I
10.1117/1.3555180
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fiber-based multimodal imaging system that combines multiphoton microscopy (MPM) with Fourier domain optical coherence microscopy (OCM) is reported. The system uses a fiber-based femtosecond laser, a fiber coupler, and a double-clad fiber (DCF) device. The fiber laser has a central wavelength of 1.04 mu m and bandwidth of 29 nm. Longer excitation wavelength is used to increase penetration depth and increase the excitation efficiency for dyes, such as red fluorescent dyes. A single mode fiber coupler is used to replace the free-space beam splitter and one arm of the coupler is fused with a double-clad fiber device. The MPM and OCM share the same excitation light path in the core of a double-clad fiber, while the OCM and MPM signals were collected by the core and clad of the double-clad fiber, respectively. The performance of the introduced double-clad device is analyzed. The device can confine all the excitation light in the core and has a collection efficiency of 20% for the MPM signal. The efficiency can be further increased by fusing more multimode fibers with the DCF. Simultaneous optical coherence microscopic imaging, second harmonic generation imaging, and two-photon excitation fluorescence imaging are demonstrated in biological samples. (C) 2011 Society of Photo-Optical Instrumentation Engineers (SPIE). [DOI: 10.1117/1.3555180]
引用
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页数:4
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