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Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases
Ocular surface diseases (OSD) can cause serious visual deterioration and discomfort. Commercial artificial tear solution containing hyaluronic acid (HA) show excellent biocompatibility and unique viscoelastic characteristics. Here, we developed a novel HA membrane (HAM) by chemical crosslinking usin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840674/ https://www.ncbi.nlm.nih.gov/pubmed/33504908 http://dx.doi.org/10.1038/s41598-021-81983-1 |
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author | Kim, Dong Ju Jung, Mi-Young Pak, Ha-Jin Park, Joo-Hee Kim, Martha Chuck, Roy S. Park, Choul Yong |
author_facet | Kim, Dong Ju Jung, Mi-Young Pak, Ha-Jin Park, Joo-Hee Kim, Martha Chuck, Roy S. Park, Choul Yong |
author_sort | Kim, Dong Ju |
collection | PubMed |
description | Ocular surface diseases (OSD) can cause serious visual deterioration and discomfort. Commercial artificial tear solution containing hyaluronic acid (HA) show excellent biocompatibility and unique viscoelastic characteristics. Here, we developed a novel HA membrane (HAM) by chemical crosslinking using 1,4-butanediol diglycidyl ether for the effective treatment of OSDs. The main purpose of HAMs is to provide sustained release of HA to modulate the wound healing response in OSDs. The safety and efficacy of HAMs were investigated using primary cultured human corneal epithelial cells and various OSD rabbit models. In the dry state, the HAM is firm, transparent, and easy to manipulate. When hydrated, it swells rapidly with high water retention and over 90% transmission of visible light. Human corneal epithelial cells and rabbit eyes showed no toxic response to HAM. Addition of HAMs to the culture medium enhanced human corneal epithelial cell viability and expression of cell proliferation markers. Investigation of HAM wound healing efficacy using mechanical or chemical corneal trauma and conjunctival surgery in rabbits revealed that application of HAMs to the ocular surface enhanced healing of corneal epithelium and reduced corneal limbal vascularization, opacity and conjunctival fibrosis. The therapeutic potential of HAMs in various OSDs was successfully demonstrated. |
format | Online Article Text |
id | pubmed-7840674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78406742021-01-28 Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases Kim, Dong Ju Jung, Mi-Young Pak, Ha-Jin Park, Joo-Hee Kim, Martha Chuck, Roy S. Park, Choul Yong Sci Rep Article Ocular surface diseases (OSD) can cause serious visual deterioration and discomfort. Commercial artificial tear solution containing hyaluronic acid (HA) show excellent biocompatibility and unique viscoelastic characteristics. Here, we developed a novel HA membrane (HAM) by chemical crosslinking using 1,4-butanediol diglycidyl ether for the effective treatment of OSDs. The main purpose of HAMs is to provide sustained release of HA to modulate the wound healing response in OSDs. The safety and efficacy of HAMs were investigated using primary cultured human corneal epithelial cells and various OSD rabbit models. In the dry state, the HAM is firm, transparent, and easy to manipulate. When hydrated, it swells rapidly with high water retention and over 90% transmission of visible light. Human corneal epithelial cells and rabbit eyes showed no toxic response to HAM. Addition of HAMs to the culture medium enhanced human corneal epithelial cell viability and expression of cell proliferation markers. Investigation of HAM wound healing efficacy using mechanical or chemical corneal trauma and conjunctival surgery in rabbits revealed that application of HAMs to the ocular surface enhanced healing of corneal epithelium and reduced corneal limbal vascularization, opacity and conjunctival fibrosis. The therapeutic potential of HAMs in various OSDs was successfully demonstrated. Nature Publishing Group UK 2021-01-27 /pmc/articles/PMC7840674/ /pubmed/33504908 http://dx.doi.org/10.1038/s41598-021-81983-1 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Dong Ju Jung, Mi-Young Pak, Ha-Jin Park, Joo-Hee Kim, Martha Chuck, Roy S. Park, Choul Yong Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
title | Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
title_full | Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
title_fullStr | Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
title_full_unstemmed | Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
title_short | Development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
title_sort | development of a novel hyaluronic acid membrane for the treatment of ocular surface diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840674/ https://www.ncbi.nlm.nih.gov/pubmed/33504908 http://dx.doi.org/10.1038/s41598-021-81983-1 |
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