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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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 |
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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 |
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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. |
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Lee Kong Chian School of Medicine (LKCMedicine) |
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Lee Kong Chian School of Medicine (LKCMedicine) Kumar, Varun Tian, Yao Becker, David Lawrence Liu, Quan |
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Article |
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Kumar, Varun Tian, Yao Becker, David Lawrence Liu, Quan |
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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 |
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A-scan fluorescence microscopy for rapid cross-sectional imaging |
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A-scan fluorescence microscopy for rapid cross-sectional imaging |
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a-scan fluorescence microscopy for rapid cross-sectional imaging |
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2024 |
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https://hdl.handle.net/10356/181452 |
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