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Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization
Corneal neovascularization (CNV) is the major cause of blindness after eye injury; however, only several drugs can be applied and the invasive administration ways (i.e., intravitreal injection and subconjunctival injection) are used. Resveratrol is a highly effective anti-VEGF agent against CNV. How...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7832990/ https://www.ncbi.nlm.nih.gov/pubmed/33472443 http://dx.doi.org/10.1080/10717544.2021.1872739 |
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author | Li, Minshu Yu, Xiang Zhu, Lin Jin, Yiguang Wu, Zhihong |
author_facet | Li, Minshu Yu, Xiang Zhu, Lin Jin, Yiguang Wu, Zhihong |
author_sort | Li, Minshu |
collection | PubMed |
description | Corneal neovascularization (CNV) is the major cause of blindness after eye injury; however, only several drugs can be applied and the invasive administration ways (i.e., intravitreal injection and subconjunctival injection) are used. Resveratrol is a highly effective anti-VEGF agent against CNV. However, its applications are limited due to its strong hydrophobicity and instability. Here, we developed a resveratrol-loaded ocular lamellar crystalline gel (ROLG) for high inhibition of CNV. ROLGs were composed of resveratrol, glyceryl monooleate (GMO), ethanol, and water, and their lamellar crystalline structures were identified by polarizing light microscopy and small-angle X-ray scattering. High drug loading (4.4 mg/g) of ROLGs was achieved due to the hydrogen bonding between GMO and resveratrol. Resveratrol showed sustained release with 67% accumulative release in 7 h, which was attributed to the slow erosion of gels. Resveratrol in ROLGs had a high corneal permeation 3 times higher than resveratrol in hyaluronic acid suspensions (RHSs). ROLGs were administered to rats only once a day because of their strong retention on the cornea surface. ROLGs were safe due to the very little contact of ethanol in ROLGs to the cornea. CNV post-rat corneal alkaline injury was highly inhibited by ROLGs, resulting from the attenuation of corneal VEGF expression and then corneal healing was improved. The ROLG was a promising ocular medicine for the prevention of CNV. |
format | Online Article Text |
id | pubmed-7832990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-78329902021-02-02 Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization Li, Minshu Yu, Xiang Zhu, Lin Jin, Yiguang Wu, Zhihong Drug Deliv Research Article Corneal neovascularization (CNV) is the major cause of blindness after eye injury; however, only several drugs can be applied and the invasive administration ways (i.e., intravitreal injection and subconjunctival injection) are used. Resveratrol is a highly effective anti-VEGF agent against CNV. However, its applications are limited due to its strong hydrophobicity and instability. Here, we developed a resveratrol-loaded ocular lamellar crystalline gel (ROLG) for high inhibition of CNV. ROLGs were composed of resveratrol, glyceryl monooleate (GMO), ethanol, and water, and their lamellar crystalline structures were identified by polarizing light microscopy and small-angle X-ray scattering. High drug loading (4.4 mg/g) of ROLGs was achieved due to the hydrogen bonding between GMO and resveratrol. Resveratrol showed sustained release with 67% accumulative release in 7 h, which was attributed to the slow erosion of gels. Resveratrol in ROLGs had a high corneal permeation 3 times higher than resveratrol in hyaluronic acid suspensions (RHSs). ROLGs were administered to rats only once a day because of their strong retention on the cornea surface. ROLGs were safe due to the very little contact of ethanol in ROLGs to the cornea. CNV post-rat corneal alkaline injury was highly inhibited by ROLGs, resulting from the attenuation of corneal VEGF expression and then corneal healing was improved. The ROLG was a promising ocular medicine for the prevention of CNV. Taylor & Francis 2021-01-21 /pmc/articles/PMC7832990/ /pubmed/33472443 http://dx.doi.org/10.1080/10717544.2021.1872739 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Minshu Yu, Xiang Zhu, Lin Jin, Yiguang Wu, Zhihong Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
title | Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
title_full | Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
title_fullStr | Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
title_full_unstemmed | Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
title_short | Ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
title_sort | ocular lamellar crystalline gels for sustained release and enhanced permeation of resveratrol against corneal neovascularization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7832990/ https://www.ncbi.nlm.nih.gov/pubmed/33472443 http://dx.doi.org/10.1080/10717544.2021.1872739 |
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