Scattering‐Based Light‐Sheet Microscopy for Rapid Cellular Imaging of Fresh Tissue
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Final Accepted Manuscript
Affiliation
College of Optical Sciences, University of ArizonaDepartment of Biomedical Engineering, University of Arizona
Issue Date
2020-12
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WileyCitation
Nguyen, C. D., O'Neal, P. K., Kulkarni, N., Yang, E., & Kang, D. (2020). Scattering‐Based Light‐Sheet Microscopy for Rapid Cellular Imaging of Fresh Tissue. Lasers in Surgery and Medicine.Journal
Lasers in Surgery and MedicineRights
© 2020 Wiley Periodicals LLC.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background and Objectives: Light-sheet microscopy (LSM) is a novel imaging technology that has been used for imaging fluorescence contrast in basic life science research. In this paper, we have developed a scattering-based LSM (sLSM) for rapidly imaging the cellular morphology of fresh tissues without any exogenous fluorescent dyes. Study Design/Materials and Methods: In the sLSM device, a thin light sheet with the central wavelength of 834 nm was incident on the tissue obliquely, 45° relative to the tissue surface. The detection optics was configured to map the light sheet-illuminated area onto a two-dimensional imaging sensor. The illumination numerical aperture (NA) was set as 0.0625, and the detection NA 0.3. Results: The sLSM device achieved a light sheet thickness of less than 6.7 µm over 284 µm along the illumination optical axis. The detection optics of the sLSM device had a resolution of 1.8 µm. The sLSM images of the swine kidney ex vivo visualized tubules with similar sizes and shapes to those observed in histopathologic images. The swine duodenum sLSM images revealed cell nuclei and villi architecture in superficial lesions and glands in deeper regions. Conclusions: The preliminary results suggest that sLSM may have the potential for rapidly examining the freshly-excised tissue ex vivo or intact tissue in vivo at microscopic resolution. Further optimization and performance evaluation of the sLSM technology will be needed in the future. Lasers Surg. Med. © 2020 Wiley Periodicals LLC.Note
12 month embargo; first published 01 December 2020ISSN
0196-8092EISSN
1096-9101Version
Final accepted manuscriptae974a485f413a2113503eed53cd6c53
10.1002/lsm.23361