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Park, Jung-Hoon
Bio-Optics Lab.
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Open-top axially swept light-sheet microscopy

Author(s)
Kim, BumjuNa, MyeongsuPark, SoohyunKim, KitaePark, Jung-HoonChung, EuiheonChang, SunghoeKim, Ki Hean
Issued Date
2021-04
DOI
10.1364/boe.419030
URI
https://scholarworks.unist.ac.kr/handle/201301/52731
Fulltext
https://www.osapublishing.org/boe/fulltext.cfm?uri=boe-12-4-2328&id=449532
Citation
BIOMEDICAL OPTICS EXPRESS, v.12, no.4, pp.2328 - 2338
Abstract
Open-top light-sheet microscopy (OT-LSM) is a specialized microscopic technique for high throughput cellular imaging of large tissue specimens including optically cleared tissues by having the entire optical setup below the sample stage. Current OT-LSM systems had relatively low axial resolutions by using weakly focused light sheets to cover the imaging field of view (FOV). In this report, open-top axially swept LSM (OTAS-LSM) was developed for high-throughput cellular imaging with improved axial resolution. OTAS-LSM swept a tightly focused excitation light sheet across the imaging FOV using an electro tunable lens (ETL) and collected emission light at the focus of the light sheet with a camera in the rolling shutter mode. OTAS-LSM was developed by using air objective lenses and a liquid prism and it had on-axis optical aberration associated with the mismatch of refractive indices between air and immersion medium. The effects of optical aberration were analyzed by both simulation and experiment, and the image resolutions were under 1.6 & micro;m in all directions. The newly developed OTAS-LSM was applied to the imaging of optically cleared mouse brain and small intestine, and it demonstrated the single-cell resolution imaging of neuronal networks. OTAS-LSM might be useful for the high-throughput cellular examination of optically cleared large tissues.
Publisher
OPTICAL SOC AMER
ISSN
2156-7085

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