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Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments
Central nervous system (CNS) diseases represent an extreme burden with significant social and economic costs. A common link in most brain pathologies is the appearance of inflammatory components that can jeopardize the stability of the implanted biomaterials and the effectiveness of therapies. Diffe...
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/PMC10255612/ https://www.ncbi.nlm.nih.gov/pubmed/37299290 http://dx.doi.org/10.3390/polym15112491 |
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author | Yonesi, Mahdi Ramos, Milagros Ramirez-Castillejo, Carmen Fernández-Serra, Rocío Panetsos, Fivos Belarra, Adrián Chevalier, Margarita Rojo, Francisco J. Pérez-Rigueiro, José Guinea, Gustavo V. González-Nieto, Daniel |
author_facet | Yonesi, Mahdi Ramos, Milagros Ramirez-Castillejo, Carmen Fernández-Serra, Rocío Panetsos, Fivos Belarra, Adrián Chevalier, Margarita Rojo, Francisco J. Pérez-Rigueiro, José Guinea, Gustavo V. González-Nieto, Daniel |
author_sort | Yonesi, Mahdi |
collection | PubMed |
description | Central nervous system (CNS) diseases represent an extreme burden with significant social and economic costs. A common link in most brain pathologies is the appearance of inflammatory components that can jeopardize the stability of the implanted biomaterials and the effectiveness of therapies. Different silk fibroin scaffolds have been used in applications related to CNS disorders. Although some studies have analyzed the degradability of silk fibroin in non-cerebral tissues (almost exclusively upon non-inflammatory conditions), the stability of silk hydrogel scaffolds in the inflammatory nervous system has not been studied in depth. In this study, the stability of silk fibroin hydrogels exposed to different neuroinflammatory contexts has been explored using an in vitro microglial cell culture and two in vivo pathological models of cerebral stroke and Alzheimer’s disease. This biomaterial was relatively stable and did not show signs of extensive degradation across time after implantation and during two weeks of in vivo analysis. This finding contrasted with the rapid degradation observed under the same in vivo conditions for other natural materials such as collagen. Our results support the suitability of silk fibroin hydrogels for intracerebral applications and highlight the potentiality of this vehicle for the release of molecules and cells for acute and chronic treatments in cerebral pathologies. |
format | Online Article Text |
id | pubmed-10255612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102556122023-06-10 Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments Yonesi, Mahdi Ramos, Milagros Ramirez-Castillejo, Carmen Fernández-Serra, Rocío Panetsos, Fivos Belarra, Adrián Chevalier, Margarita Rojo, Francisco J. Pérez-Rigueiro, José Guinea, Gustavo V. González-Nieto, Daniel Polymers (Basel) Article Central nervous system (CNS) diseases represent an extreme burden with significant social and economic costs. A common link in most brain pathologies is the appearance of inflammatory components that can jeopardize the stability of the implanted biomaterials and the effectiveness of therapies. Different silk fibroin scaffolds have been used in applications related to CNS disorders. Although some studies have analyzed the degradability of silk fibroin in non-cerebral tissues (almost exclusively upon non-inflammatory conditions), the stability of silk hydrogel scaffolds in the inflammatory nervous system has not been studied in depth. In this study, the stability of silk fibroin hydrogels exposed to different neuroinflammatory contexts has been explored using an in vitro microglial cell culture and two in vivo pathological models of cerebral stroke and Alzheimer’s disease. This biomaterial was relatively stable and did not show signs of extensive degradation across time after implantation and during two weeks of in vivo analysis. This finding contrasted with the rapid degradation observed under the same in vivo conditions for other natural materials such as collagen. Our results support the suitability of silk fibroin hydrogels for intracerebral applications and highlight the potentiality of this vehicle for the release of molecules and cells for acute and chronic treatments in cerebral pathologies. MDPI 2023-05-28 /pmc/articles/PMC10255612/ /pubmed/37299290 http://dx.doi.org/10.3390/polym15112491 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 Yonesi, Mahdi Ramos, Milagros Ramirez-Castillejo, Carmen Fernández-Serra, Rocío Panetsos, Fivos Belarra, Adrián Chevalier, Margarita Rojo, Francisco J. Pérez-Rigueiro, José Guinea, Gustavo V. González-Nieto, Daniel Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments |
title | Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments |
title_full | Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments |
title_fullStr | Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments |
title_full_unstemmed | Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments |
title_short | Resistance to Degradation of Silk Fibroin Hydrogels Exposed to Neuroinflammatory Environments |
title_sort | resistance to degradation of silk fibroin hydrogels exposed to neuroinflammatory environments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10255612/ https://www.ncbi.nlm.nih.gov/pubmed/37299290 http://dx.doi.org/10.3390/polym15112491 |
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