A-scan fluorescence microscopy for rapid cross-sectional imaging

This paper presents a microscopy technique that can perform snapshot depth resolved optical imaging in the same manner as A-scan in ultrasound imaging and optical coherence tomography. In this technique, a laser line along the axial dimension is used to illuminate a sample to create a fluorescent li...

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Main Authors: Kumar, Varun, Tian, Yao, Becker, David Lawrence, Liu, Quan
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/181452
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1814522024-12-08T15:39:20Z A-scan fluorescence microscopy for rapid cross-sectional imaging Kumar, Varun Tian, Yao Becker, David Lawrence Liu, Quan Lee Kong Chian School of Medicine (LKCMedicine) School of Chemical and Biomedical Engineering Medicine, Health and Life Sciences Coherence tomography Cross-sectional imaging This paper presents a microscopy technique that can perform snapshot depth resolved optical imaging in the same manner as A-scan in ultrasound imaging and optical coherence tomography. In this technique, a laser line along the axial dimension is used to illuminate a sample to create a fluorescent line object. By transforming the line object along the axial dimension (Z) to a ring image on the lateral dimensions (X-Y) using a full cone mirror, common optics can be used to relay and acquire the ring image precisely. Then, by converting half of the ring image back to a line image using a half cone mirror, the opening side of the half cone mirror allows the line image, which contains the full depth resolved information of the line object, to be taken in one snapshot. This eliminates the requirement of axial scanning in traditional depth resolved imaging techniques such as confocal microscopy to obtain the same information. The technique is demonstrated by imaging fluorescent microspheres of different diameters. This technique offers a simple alternative to traditional depth resolved imaging techniques such as confocal microscopy and light sheet microscopy. It is particularly useful in imaging samples with multiple layers in which multiple A-scans or a few B-scans are sufficient to represent the entire sample. Published version This work was partially supported by the National Natural Science Foundation of China (Grant No. 32250006), the Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM) under Grant HRTP-[2022]-46, Fujian Minjiang Distinguished Scholar Program, Fujian High-level Innovative Talent Program, and Xiamen High-Level Innovative Talent Program of Double Hundred Plan, China. 2024-12-02T08:01:36Z 2024-12-02T08:01:36Z 2024 Journal Article Kumar, V., Tian, Y., Becker, D. L. & Liu, Q. (2024). A-scan fluorescence microscopy for rapid cross-sectional imaging. Applied Physics Letters, 125(11). https://dx.doi.org/10.1063/5.0215650 0003-6951 https://hdl.handle.net/10356/181452 10.1063/5.0215650 2-s2.0-85203654332 11 125 en Applied Physics Letters © 2024 Author(s). Published under an exclusive license by AIP Publishing. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1063/5.0215650 application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Medicine, Health and Life Sciences
Coherence tomography
Cross-sectional imaging
spellingShingle Medicine, Health and Life Sciences
Coherence tomography
Cross-sectional imaging
Kumar, Varun
Tian, Yao
Becker, David Lawrence
Liu, Quan
A-scan fluorescence microscopy for rapid cross-sectional imaging
description This paper presents a microscopy technique that can perform snapshot depth resolved optical imaging in the same manner as A-scan in ultrasound imaging and optical coherence tomography. In this technique, a laser line along the axial dimension is used to illuminate a sample to create a fluorescent line object. By transforming the line object along the axial dimension (Z) to a ring image on the lateral dimensions (X-Y) using a full cone mirror, common optics can be used to relay and acquire the ring image precisely. Then, by converting half of the ring image back to a line image using a half cone mirror, the opening side of the half cone mirror allows the line image, which contains the full depth resolved information of the line object, to be taken in one snapshot. This eliminates the requirement of axial scanning in traditional depth resolved imaging techniques such as confocal microscopy to obtain the same information. The technique is demonstrated by imaging fluorescent microspheres of different diameters. This technique offers a simple alternative to traditional depth resolved imaging techniques such as confocal microscopy and light sheet microscopy. It is particularly useful in imaging samples with multiple layers in which multiple A-scans or a few B-scans are sufficient to represent the entire sample.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Kumar, Varun
Tian, Yao
Becker, David Lawrence
Liu, Quan
format Article
author Kumar, Varun
Tian, Yao
Becker, David Lawrence
Liu, Quan
author_sort Kumar, Varun
title A-scan fluorescence microscopy for rapid cross-sectional imaging
title_short A-scan fluorescence microscopy for rapid cross-sectional imaging
title_full A-scan fluorescence microscopy for rapid cross-sectional imaging
title_fullStr A-scan fluorescence microscopy for rapid cross-sectional imaging
title_full_unstemmed A-scan fluorescence microscopy for rapid cross-sectional imaging
title_sort a-scan fluorescence microscopy for rapid cross-sectional imaging
publishDate 2024
url https://hdl.handle.net/10356/181452
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