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Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use

Preclinical and clinical diagnostics increasingly rely on techniques to visualize internal organs at high resolution via endoscopes. Miniaturized endoscopic probes are necessary for imaging small luminal or delicate organs without causing trauma to tissue. However, current fabrication methods limit...

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Autores principales: Li, Jiawen, Thiele, Simon, Quirk, Bryden C., Kirk, Rodney W., Verjans, Johan W., Akers, Emma, Bursill, Christina A., Nicholls, Stephen J., Herkommer, Alois M., Giessen, Harald, McLaughlin, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371638/
https://www.ncbi.nlm.nih.gov/pubmed/32704357
http://dx.doi.org/10.1038/s41377-020-00365-w
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author Li, Jiawen
Thiele, Simon
Quirk, Bryden C.
Kirk, Rodney W.
Verjans, Johan W.
Akers, Emma
Bursill, Christina A.
Nicholls, Stephen J.
Herkommer, Alois M.
Giessen, Harald
McLaughlin, Robert A.
author_facet Li, Jiawen
Thiele, Simon
Quirk, Bryden C.
Kirk, Rodney W.
Verjans, Johan W.
Akers, Emma
Bursill, Christina A.
Nicholls, Stephen J.
Herkommer, Alois M.
Giessen, Harald
McLaughlin, Robert A.
author_sort Li, Jiawen
collection PubMed
description Preclinical and clinical diagnostics increasingly rely on techniques to visualize internal organs at high resolution via endoscopes. Miniaturized endoscopic probes are necessary for imaging small luminal or delicate organs without causing trauma to tissue. However, current fabrication methods limit the imaging performance of highly miniaturized probes, restricting their widespread application. To overcome this limitation, we developed a novel ultrathin probe fabrication technique that utilizes 3D microprinting to reliably create side-facing freeform micro-optics (<130 µm diameter) on single-mode fibers. Using this technique, we built a fully functional ultrathin aberration-corrected optical coherence tomography probe. This is the smallest freeform 3D imaging probe yet reported, with a diameter of 0.457 mm, including the catheter sheath. We demonstrated image quality and mechanical flexibility by imaging atherosclerotic human and mouse arteries. The ability to provide microstructural information with the smallest optical coherence tomography catheter opens a gateway for novel minimally invasive applications in disease.
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spelling pubmed-73716382020-07-22 Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use Li, Jiawen Thiele, Simon Quirk, Bryden C. Kirk, Rodney W. Verjans, Johan W. Akers, Emma Bursill, Christina A. Nicholls, Stephen J. Herkommer, Alois M. Giessen, Harald McLaughlin, Robert A. Light Sci Appl Article Preclinical and clinical diagnostics increasingly rely on techniques to visualize internal organs at high resolution via endoscopes. Miniaturized endoscopic probes are necessary for imaging small luminal or delicate organs without causing trauma to tissue. However, current fabrication methods limit the imaging performance of highly miniaturized probes, restricting their widespread application. To overcome this limitation, we developed a novel ultrathin probe fabrication technique that utilizes 3D microprinting to reliably create side-facing freeform micro-optics (<130 µm diameter) on single-mode fibers. Using this technique, we built a fully functional ultrathin aberration-corrected optical coherence tomography probe. This is the smallest freeform 3D imaging probe yet reported, with a diameter of 0.457 mm, including the catheter sheath. We demonstrated image quality and mechanical flexibility by imaging atherosclerotic human and mouse arteries. The ability to provide microstructural information with the smallest optical coherence tomography catheter opens a gateway for novel minimally invasive applications in disease. Nature Publishing Group UK 2020-07-20 /pmc/articles/PMC7371638/ /pubmed/32704357 http://dx.doi.org/10.1038/s41377-020-00365-w Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Jiawen
Thiele, Simon
Quirk, Bryden C.
Kirk, Rodney W.
Verjans, Johan W.
Akers, Emma
Bursill, Christina A.
Nicholls, Stephen J.
Herkommer, Alois M.
Giessen, Harald
McLaughlin, Robert A.
Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
title Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
title_full Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
title_fullStr Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
title_full_unstemmed Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
title_short Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
title_sort ultrathin monolithic 3d printed optical coherence tomography endoscopy for preclinical and clinical use
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371638/
https://www.ncbi.nlm.nih.gov/pubmed/32704357
http://dx.doi.org/10.1038/s41377-020-00365-w
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