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OCT-based label-free in vivo lymphangiography within human skin and areola

Due to the limitations of current imaging techniques, visualization of lymphatic capillaries within tissue in vivo has been challenging. Here, we present a label-free high resolution optical coherence tomography (OCT) based lymphangiography (OLAG) within human skin in vivo. OLAG enables rapid (~seco...

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Autores principales: Baran, Utku, Qin, Wan, Qi, Xiaoli, Kalkan, Goknur, Wang, Ruikang K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759696/
https://www.ncbi.nlm.nih.gov/pubmed/26892830
http://dx.doi.org/10.1038/srep21122
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author Baran, Utku
Qin, Wan
Qi, Xiaoli
Kalkan, Goknur
Wang, Ruikang K.
author_facet Baran, Utku
Qin, Wan
Qi, Xiaoli
Kalkan, Goknur
Wang, Ruikang K.
author_sort Baran, Utku
collection PubMed
description Due to the limitations of current imaging techniques, visualization of lymphatic capillaries within tissue in vivo has been challenging. Here, we present a label-free high resolution optical coherence tomography (OCT) based lymphangiography (OLAG) within human skin in vivo. OLAG enables rapid (~seconds) mapping of lymphatic networks, along with blood vessel networks, over 8 mm x 8 mm of human skin and 5 mm x 5 mm of human areola. Moreover, lymphatic system’s response to inflammation within human skin is monitored throughout an acne lesion development over 7 days. The demonstrated results promise OLAG as a revolutionary tool in the clinical research and treatment of patients with pathologic conditions such as cancer, diabetes, and autoimmune diseases.
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spelling pubmed-47596962016-02-29 OCT-based label-free in vivo lymphangiography within human skin and areola Baran, Utku Qin, Wan Qi, Xiaoli Kalkan, Goknur Wang, Ruikang K. Sci Rep Article Due to the limitations of current imaging techniques, visualization of lymphatic capillaries within tissue in vivo has been challenging. Here, we present a label-free high resolution optical coherence tomography (OCT) based lymphangiography (OLAG) within human skin in vivo. OLAG enables rapid (~seconds) mapping of lymphatic networks, along with blood vessel networks, over 8 mm x 8 mm of human skin and 5 mm x 5 mm of human areola. Moreover, lymphatic system’s response to inflammation within human skin is monitored throughout an acne lesion development over 7 days. The demonstrated results promise OLAG as a revolutionary tool in the clinical research and treatment of patients with pathologic conditions such as cancer, diabetes, and autoimmune diseases. Nature Publishing Group 2016-02-19 /pmc/articles/PMC4759696/ /pubmed/26892830 http://dx.doi.org/10.1038/srep21122 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Baran, Utku
Qin, Wan
Qi, Xiaoli
Kalkan, Goknur
Wang, Ruikang K.
OCT-based label-free in vivo lymphangiography within human skin and areola
title OCT-based label-free in vivo lymphangiography within human skin and areola
title_full OCT-based label-free in vivo lymphangiography within human skin and areola
title_fullStr OCT-based label-free in vivo lymphangiography within human skin and areola
title_full_unstemmed OCT-based label-free in vivo lymphangiography within human skin and areola
title_short OCT-based label-free in vivo lymphangiography within human skin and areola
title_sort oct-based label-free in vivo lymphangiography within human skin and areola
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759696/
https://www.ncbi.nlm.nih.gov/pubmed/26892830
http://dx.doi.org/10.1038/srep21122
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