A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation
Tissue transplantations are often associated with severe infections. Cornea replacement as the most frequent transplantation worldwide bears the risk of keratitis caused by herpes simplex virus (HSV), posing a severe and sight‐threatening complication. To overcome the current lack of effective HSV t...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
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Wiley-VCH
2023-03-01
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Series: | Advanced NanoBiomed Research |
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Online Access: | https://doi.org/10.1002/anbr.202200098 |
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author | Felix Rohde Marcel Walther Florentin Baur Maike Windbergs |
author_facet | Felix Rohde Marcel Walther Florentin Baur Maike Windbergs |
author_sort | Felix Rohde |
collection | DOAJ |
description | Tissue transplantations are often associated with severe infections. Cornea replacement as the most frequent transplantation worldwide bears the risk of keratitis caused by herpes simplex virus (HSV), posing a severe and sight‐threatening complication. To overcome the current lack of effective HSV therapy in the eye, biodegradable nanofibrous scaffolds incorporating acyclovir (ACV) intended for transplantation along with the cornea graft to prevent viral infections are designed. The rational development of these matrices reveals the strong dependency of the surface wettability on the release kinetics of the tested biocompatible poly(lactic‐co‐glycolic acid) (PLGA) polymers. Using a mixture of two PLGA polymers, a tailor‐made release of the antiviral active ACV is achieved for the intended treatment period. In a human in vitro HSV infection model, a synergistic viral inhibition mechanism by binding the virus particles on the fibers surface, while simultaneously releasing the antiviral active, could be confirmed. Besides the controlled ACV release, the polymer fibers bind virus particles to their surface, significantly reducing the virus titer. Based on this tunable dual effect, the fiber scaffolds exhibit a promising antiviral drug delivery platform, which can overcome the limitations of current infection therapy associated with cornea transplantation. |
first_indexed | 2024-04-10T04:26:15Z |
format | Article |
id | doaj.art-7937ecfefe4b47b4a995975655c2e50c |
institution | Directory Open Access Journal |
issn | 2699-9307 |
language | English |
last_indexed | 2024-04-10T04:26:15Z |
publishDate | 2023-03-01 |
publisher | Wiley-VCH |
record_format | Article |
series | Advanced NanoBiomed Research |
spelling | doaj.art-7937ecfefe4b47b4a995975655c2e50c2023-03-10T13:51:13ZengWiley-VCHAdvanced NanoBiomed Research2699-93072023-03-0133n/an/a10.1002/anbr.202200098A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal TransplantationFelix Rohde0Marcel Walther1Florentin Baur2Maike Windbergs3Institute of Pharmaceutical Technology and Buchmann Institute for Molecular Life Sciences Goethe University Frankfurt Max-von-Laue-Str. 9 60438 Frankfurt am Main GermanyInstitute of Pharmaceutical Technology and Buchmann Institute for Molecular Life Sciences Goethe University Frankfurt Max-von-Laue-Str. 9 60438 Frankfurt am Main GermanyInstitute of Pharmaceutical Technology and Buchmann Institute for Molecular Life Sciences Goethe University Frankfurt Max-von-Laue-Str. 9 60438 Frankfurt am Main GermanyInstitute of Pharmaceutical Technology and Buchmann Institute for Molecular Life Sciences Goethe University Frankfurt Max-von-Laue-Str. 9 60438 Frankfurt am Main GermanyTissue transplantations are often associated with severe infections. Cornea replacement as the most frequent transplantation worldwide bears the risk of keratitis caused by herpes simplex virus (HSV), posing a severe and sight‐threatening complication. To overcome the current lack of effective HSV therapy in the eye, biodegradable nanofibrous scaffolds incorporating acyclovir (ACV) intended for transplantation along with the cornea graft to prevent viral infections are designed. The rational development of these matrices reveals the strong dependency of the surface wettability on the release kinetics of the tested biocompatible poly(lactic‐co‐glycolic acid) (PLGA) polymers. Using a mixture of two PLGA polymers, a tailor‐made release of the antiviral active ACV is achieved for the intended treatment period. In a human in vitro HSV infection model, a synergistic viral inhibition mechanism by binding the virus particles on the fibers surface, while simultaneously releasing the antiviral active, could be confirmed. Besides the controlled ACV release, the polymer fibers bind virus particles to their surface, significantly reducing the virus titer. Based on this tunable dual effect, the fiber scaffolds exhibit a promising antiviral drug delivery platform, which can overcome the limitations of current infection therapy associated with cornea transplantation.https://doi.org/10.1002/anbr.202200098drug deliveryelectrospinningherpes keratitisherpes simplex virusocular implantsynergistic inhibition |
spellingShingle | Felix Rohde Marcel Walther Florentin Baur Maike Windbergs A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation Advanced NanoBiomed Research drug delivery electrospinning herpes keratitis herpes simplex virus ocular implant synergistic inhibition |
title | A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation |
title_full | A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation |
title_fullStr | A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation |
title_full_unstemmed | A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation |
title_short | A Dual‐Function Electrospun Matrix for the Prevention of Herpes Simplex Virus‐1 Infections after Corneal Transplantation |
title_sort | dual function electrospun matrix for the prevention of herpes simplex virus 1 infections after corneal transplantation |
topic | drug delivery electrospinning herpes keratitis herpes simplex virus ocular implant synergistic inhibition |
url | https://doi.org/10.1002/anbr.202200098 |
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