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• W2772298524 abstract "Optical sectioning imaging with high spatial resolution deep inside scattering samples such as mammalian brain is of great interest in biological study. Conventional two-photon microscopy deteriorates in focus when light scattering increases. Here we develop an optical sectioning enhanced two-photon technique which incorporates structured illumination into line-scanning spatial-temporal focusing microscopy (LTSIM), and generate patterned illumination via laser intensity modulation synchronized with scanning. LTSIM brings scattering background elimination and in-focus contrast enhancement, and realizes nearly 2-fold increase in spatial resolution to ∼208 nm laterally and ∼0.94 µm axially. In addition, the intensity modulated line-scanning implementation of LTSIM enables fast and flexible generation of structured illumination, permitting adjustable spatial frequency profiles to optimize image contrast. The highly qualified optical sectioning ability of our system is demonstrated on samples including tissue phantom, C. elegans and mouse brain at depths over hundreds of microns." @default.
• W2772298524 created "2017-12-22" @default.
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• W2772298524 date "2017-12-07" @default.
• W2772298524 modified "2023-10-16" @default.
• W2772298524 title "Contrast and resolution enhanced optical sectioning in scattering tissue using line-scanning two-photon structured illumination microscopy" @default.
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• W2772298524 doi "https://doi.org/10.1364/oe.25.032010" @default.
• W2772298524 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29245869" @default.
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