Paper
18 April 2017 Two-photon excitation microscopy with spatial light modulator
Naoya Matsumoto, Alu Konno, Takashi Inoue, Haruyoshi Toyoda, Toshiyuki Miwa, Kazuhiro Nakamura, Shigetoshi Okazaki
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Abstract
We attempted to observe deep regions in biological samples through two-photon excitation microscopy adopting a spatial light modulator (SLM). The SLM is used for correcting spherical aberration (SA) caused by the refractive-index mismatch between the immersion medium and sample. In the observation of fluorescent beads in transparent epoxy resin, the fluorescence intensity from a scan with SA correction was 50 times that from a scan without SA correction. After that, we observed blood vessels in a mouse brain, which became transparent with a clearing agent.
© (2017) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Naoya Matsumoto, Alu Konno, Takashi Inoue, Haruyoshi Toyoda, Toshiyuki Miwa, Kazuhiro Nakamura, and Shigetoshi Okazaki "Two-photon excitation microscopy with spatial light modulator", Proc. SPIE 10251, Biomedical Imaging and Sensing Conference, 1025105 (18 April 2017); https://doi.org/10.1117/12.2269406
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KEYWORDS
Wavefronts

Spatial light modulators

Luminescence

Objectives

Two photon excitation microscopy

Epoxies

Modulation

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