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Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior

In craniofacial tissue regeneration, the current gold standard treatment is autologous bone grafting, however, it presents some disadvantages. Although new alternatives have emerged there is still an urgent demand of biodegradable scaffolds to act as extracellular matrix in the regeneration process....

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Autores principales: Rodríguez-Méndez, Itzia, Fernández-Gutiérrez, Mar, Rodríguez-Navarrete, Amairany, Rosales-Ibáñez, Raúl, Benito-Garzón, Lorena, Vázquez-Lasa, Blanca, San Román, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415099/
https://www.ncbi.nlm.nih.gov/pubmed/30966314
http://dx.doi.org/10.3390/polym10030279
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author Rodríguez-Méndez, Itzia
Fernández-Gutiérrez, Mar
Rodríguez-Navarrete, Amairany
Rosales-Ibáñez, Raúl
Benito-Garzón, Lorena
Vázquez-Lasa, Blanca
San Román, Julio
author_facet Rodríguez-Méndez, Itzia
Fernández-Gutiérrez, Mar
Rodríguez-Navarrete, Amairany
Rosales-Ibáñez, Raúl
Benito-Garzón, Lorena
Vázquez-Lasa, Blanca
San Román, Julio
author_sort Rodríguez-Méndez, Itzia
collection PubMed
description In craniofacial tissue regeneration, the current gold standard treatment is autologous bone grafting, however, it presents some disadvantages. Although new alternatives have emerged there is still an urgent demand of biodegradable scaffolds to act as extracellular matrix in the regeneration process. A potentially useful element in bone regeneration is strontium. It is known to promote stimulation of osteoblasts while inhibiting osteoclasts resorption, leading to neoformed bone. The present paper reports the preparation and characterization of strontium (Sr) containing hybrid scaffolds formed by a matrix of ionically cross-linked chitosan and microparticles of poly(ε-caprolactone) (PCL). These scaffolds of relatively facile fabrication were seeded with osteoblast-like cells (MG-63) and human bone marrow mesenchymal stem cells (hBMSCs) for application in craniofacial tissue regeneration. Membrane scaffolds were prepared using chitosan:PCL ratios of 1:2 and 1:1 and 5 wt % Sr salts. Characterization was performed addressing physico-chemical properties, swelling behavior, in vitro biological performance and in vivo biocompatibility. Overall, the composition, microstructure and swelling degree (≈245%) of scaffolds combine with the adequate dimensional stability, lack of toxicity, osteogenic activity in MG-63 cells and hBMSCs, along with the in vivo biocompatibility in rats allow considering this system as a promising biomaterial for the treatment of craniofacial tissue regeneration.
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spelling pubmed-64150992019-04-02 Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior Rodríguez-Méndez, Itzia Fernández-Gutiérrez, Mar Rodríguez-Navarrete, Amairany Rosales-Ibáñez, Raúl Benito-Garzón, Lorena Vázquez-Lasa, Blanca San Román, Julio Polymers (Basel) Article In craniofacial tissue regeneration, the current gold standard treatment is autologous bone grafting, however, it presents some disadvantages. Although new alternatives have emerged there is still an urgent demand of biodegradable scaffolds to act as extracellular matrix in the regeneration process. A potentially useful element in bone regeneration is strontium. It is known to promote stimulation of osteoblasts while inhibiting osteoclasts resorption, leading to neoformed bone. The present paper reports the preparation and characterization of strontium (Sr) containing hybrid scaffolds formed by a matrix of ionically cross-linked chitosan and microparticles of poly(ε-caprolactone) (PCL). These scaffolds of relatively facile fabrication were seeded with osteoblast-like cells (MG-63) and human bone marrow mesenchymal stem cells (hBMSCs) for application in craniofacial tissue regeneration. Membrane scaffolds were prepared using chitosan:PCL ratios of 1:2 and 1:1 and 5 wt % Sr salts. Characterization was performed addressing physico-chemical properties, swelling behavior, in vitro biological performance and in vivo biocompatibility. Overall, the composition, microstructure and swelling degree (≈245%) of scaffolds combine with the adequate dimensional stability, lack of toxicity, osteogenic activity in MG-63 cells and hBMSCs, along with the in vivo biocompatibility in rats allow considering this system as a promising biomaterial for the treatment of craniofacial tissue regeneration. MDPI 2018-03-07 /pmc/articles/PMC6415099/ /pubmed/30966314 http://dx.doi.org/10.3390/polym10030279 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rodríguez-Méndez, Itzia
Fernández-Gutiérrez, Mar
Rodríguez-Navarrete, Amairany
Rosales-Ibáñez, Raúl
Benito-Garzón, Lorena
Vázquez-Lasa, Blanca
San Román, Julio
Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior
title Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior
title_full Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior
title_fullStr Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior
title_full_unstemmed Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior
title_short Bioactive Sr(II)/Chitosan/Poly(ε-caprolactone) Scaffolds for Craniofacial Tissue Regeneration. In Vitro and In Vivo Behavior
title_sort bioactive sr(ii)/chitosan/poly(ε-caprolactone) scaffolds for craniofacial tissue regeneration. in vitro and in vivo behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415099/
https://www.ncbi.nlm.nih.gov/pubmed/30966314
http://dx.doi.org/10.3390/polym10030279
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