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Fast 3D visualization of endogenous brain signals with high-sensitivity laser scanning photothermal microscopy.


ABSTRACT: A fast, high-sensitivity photothermal microscope was developed by implementing a spatially segmented balanced detection scheme into a laser scanning microscope. We confirmed a 4.9 times improvement in signal-to-noise ratio in the spatially segmented balanced detection compared with that of conventional detection. The system demonstrated simultaneous bi-modal photothermal and confocal fluorescence imaging of transgenic mouse brain tissue with a pixel dwell time of 20 ?s. The fluorescence image visualized neurons expressing yellow fluorescence proteins, while the photothermal signal detected endogenous chromophores in the mouse brain, allowing 3D visualization of the distribution of various features such as blood cells and fine structures probably due to lipids. This imaging modality was constructed using compact and cost-effective laser diodes, and will thus be widely useful in the life and medical sciences.

SUBMITTER: Miyazaki J 

PROVIDER: S-EPMC4871075 | biostudies-literature | 2016 May

REPOSITORIES: biostudies-literature

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Fast 3D visualization of endogenous brain signals with high-sensitivity laser scanning photothermal microscopy.

Miyazaki Jun J   Iida Tadatsune T   Tanaka Shinji S   Hayashi-Takagi Akiko A   Kasai Haruo H   Okabe Shigeo S   Kobayashi Takayoshi T  

Biomedical optics express 20160405 5


A fast, high-sensitivity photothermal microscope was developed by implementing a spatially segmented balanced detection scheme into a laser scanning microscope. We confirmed a 4.9 times improvement in signal-to-noise ratio in the spatially segmented balanced detection compared with that of conventional detection. The system demonstrated simultaneous bi-modal photothermal and confocal fluorescence imaging of transgenic mouse brain tissue with a pixel dwell time of 20 μs. The fluorescence image vi  ...[more]

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