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Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging
The clinical outcome of corneal collagen crosslinking (CXL) is typically evaluated several weeks after treatment. An earlier assessment of its outcome could lead to an optimization of the treatment, including an immediate re-intervention in case of failure, thereby, avoiding additional discomfort an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629644/ https://www.ncbi.nlm.nih.gov/pubmed/31308406 http://dx.doi.org/10.1038/s41598-019-46572-3 |
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author | Batista, Ana Breunig, Hans Georg Hager, Tobias Seitz, Berthold König, Karsten |
author_facet | Batista, Ana Breunig, Hans Georg Hager, Tobias Seitz, Berthold König, Karsten |
author_sort | Batista, Ana |
collection | PubMed |
description | The clinical outcome of corneal collagen crosslinking (CXL) is typically evaluated several weeks after treatment. An earlier assessment of its outcome could lead to an optimization of the treatment, including an immediate re-intervention in case of failure, thereby, avoiding additional discomfort and pain to the patient. In this study, we propose two-photon imaging (TPI) as an earlier evaluation method. CXL was performed in human corneas by application of riboflavin followed by UVA irradiation. Autofluorescence (AF) intensity and lifetime images were acquired using a commercial clinically certified multiphoton tomograph prior to CXL and after 2h, 24h, 72h, and 144h storage in culture medium. The first monitoring point was determined as the minimum time required for riboflavin clearance from the cornea. As control, untreated samples and samples treated only with riboflavin (without UVA irradiation) were monitored at the same time points. Significant increases in the stroma AF intensity and lifetime were observed as soon as 2h after treatment. A depth-dependent TPI analysis showed higher AF lifetimes anteriorly corresponding to areas were CXL was most effective. No alterations were observed in the control groups. Using TPI, the outcome of CXL can be assessed non-invasively and label-free much sooner than with conventional clinical devices. |
format | Online Article Text |
id | pubmed-6629644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66296442019-07-23 Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging Batista, Ana Breunig, Hans Georg Hager, Tobias Seitz, Berthold König, Karsten Sci Rep Article The clinical outcome of corneal collagen crosslinking (CXL) is typically evaluated several weeks after treatment. An earlier assessment of its outcome could lead to an optimization of the treatment, including an immediate re-intervention in case of failure, thereby, avoiding additional discomfort and pain to the patient. In this study, we propose two-photon imaging (TPI) as an earlier evaluation method. CXL was performed in human corneas by application of riboflavin followed by UVA irradiation. Autofluorescence (AF) intensity and lifetime images were acquired using a commercial clinically certified multiphoton tomograph prior to CXL and after 2h, 24h, 72h, and 144h storage in culture medium. The first monitoring point was determined as the minimum time required for riboflavin clearance from the cornea. As control, untreated samples and samples treated only with riboflavin (without UVA irradiation) were monitored at the same time points. Significant increases in the stroma AF intensity and lifetime were observed as soon as 2h after treatment. A depth-dependent TPI analysis showed higher AF lifetimes anteriorly corresponding to areas were CXL was most effective. No alterations were observed in the control groups. Using TPI, the outcome of CXL can be assessed non-invasively and label-free much sooner than with conventional clinical devices. Nature Publishing Group UK 2019-07-15 /pmc/articles/PMC6629644/ /pubmed/31308406 http://dx.doi.org/10.1038/s41598-019-46572-3 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Batista, Ana Breunig, Hans Georg Hager, Tobias Seitz, Berthold König, Karsten Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
title | Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
title_full | Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
title_fullStr | Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
title_full_unstemmed | Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
title_short | Early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
title_sort | early evaluation of corneal collagen crosslinking in ex-vivo human corneas using two-photon imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629644/ https://www.ncbi.nlm.nih.gov/pubmed/31308406 http://dx.doi.org/10.1038/s41598-019-46572-3 |
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