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Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration
Corneal pathologies from infectious or noninfectious origin have a significant impact on the daily lives of millions of people worldwide. Despite the risk of organ rejection or infection, corneal transplantation is currently the only effective treatment. Finding safe and innovative strategies is the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854711/ https://www.ncbi.nlm.nih.gov/pubmed/36671634 http://dx.doi.org/10.3390/bioengineering10010062 |
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author | Alves, Ana L. Carvalho, Ana C. Machado, Inês Diogo, Gabriela S. Fernandes, Emanuel M. Castro, Vânia I. B. Pires, Ricardo A. Vázquez, José A. Pérez-Martín, Ricardo I. Alaminos, Miguel Reis, Rui L. Silva, Tiago H. |
author_facet | Alves, Ana L. Carvalho, Ana C. Machado, Inês Diogo, Gabriela S. Fernandes, Emanuel M. Castro, Vânia I. B. Pires, Ricardo A. Vázquez, José A. Pérez-Martín, Ricardo I. Alaminos, Miguel Reis, Rui L. Silva, Tiago H. |
author_sort | Alves, Ana L. |
collection | PubMed |
description | Corneal pathologies from infectious or noninfectious origin have a significant impact on the daily lives of millions of people worldwide. Despite the risk of organ rejection or infection, corneal transplantation is currently the only effective treatment. Finding safe and innovative strategies is the main goal of tissue-engineering-based approaches. In this study, the potential of gelatin methacryloyl (GelMA) hydrogels produced from marine-derived gelatin and loaded with ascorbic acid (as an enhancer of the biological activity of cells) was evaluated for corneal stromal applications. Marine GelMA was synthesized with a methacrylation degree of 75%, enabling effective photocrosslinking, and hydrogels with or without ascorbic acid were produced, encompassing human keratocytes. All the produced formulations exhibited excellent optical and swelling properties with easy handling as well as structural stability and adequate degradation rates that may allow proper extracellular matrix remodeling by corneal stromal cells. Formulations loaded with 0.5 mg/mL of ascorbic acid enhanced the biological performance of keratocytes and induced collagen production. These results suggest that, in addition to marine-derived gelatin being suitable for the synthesis of GelMA, the hydrogels produced are promising biomaterials for corneal regeneration applications. |
format | Online Article Text |
id | pubmed-9854711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98547112023-01-21 Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration Alves, Ana L. Carvalho, Ana C. Machado, Inês Diogo, Gabriela S. Fernandes, Emanuel M. Castro, Vânia I. B. Pires, Ricardo A. Vázquez, José A. Pérez-Martín, Ricardo I. Alaminos, Miguel Reis, Rui L. Silva, Tiago H. Bioengineering (Basel) Article Corneal pathologies from infectious or noninfectious origin have a significant impact on the daily lives of millions of people worldwide. Despite the risk of organ rejection or infection, corneal transplantation is currently the only effective treatment. Finding safe and innovative strategies is the main goal of tissue-engineering-based approaches. In this study, the potential of gelatin methacryloyl (GelMA) hydrogels produced from marine-derived gelatin and loaded with ascorbic acid (as an enhancer of the biological activity of cells) was evaluated for corneal stromal applications. Marine GelMA was synthesized with a methacrylation degree of 75%, enabling effective photocrosslinking, and hydrogels with or without ascorbic acid were produced, encompassing human keratocytes. All the produced formulations exhibited excellent optical and swelling properties with easy handling as well as structural stability and adequate degradation rates that may allow proper extracellular matrix remodeling by corneal stromal cells. Formulations loaded with 0.5 mg/mL of ascorbic acid enhanced the biological performance of keratocytes and induced collagen production. These results suggest that, in addition to marine-derived gelatin being suitable for the synthesis of GelMA, the hydrogels produced are promising biomaterials for corneal regeneration applications. MDPI 2023-01-04 /pmc/articles/PMC9854711/ /pubmed/36671634 http://dx.doi.org/10.3390/bioengineering10010062 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alves, Ana L. Carvalho, Ana C. Machado, Inês Diogo, Gabriela S. Fernandes, Emanuel M. Castro, Vânia I. B. Pires, Ricardo A. Vázquez, José A. Pérez-Martín, Ricardo I. Alaminos, Miguel Reis, Rui L. Silva, Tiago H. Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration |
title | Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration |
title_full | Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration |
title_fullStr | Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration |
title_full_unstemmed | Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration |
title_short | Cell-Laden Marine Gelatin Methacryloyl Hydrogels Enriched with Ascorbic Acid for Corneal Stroma Regeneration |
title_sort | cell-laden marine gelatin methacryloyl hydrogels enriched with ascorbic acid for corneal stroma regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854711/ https://www.ncbi.nlm.nih.gov/pubmed/36671634 http://dx.doi.org/10.3390/bioengineering10010062 |
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