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In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model
Zinc-enriched mesoporous bioactive glasses (MBGs) are bioceramics with potential antibacterial and osteogenic properties. However, few assays have been performed to study these properties in animal models. In this study, MBGs enriched with up to 5% ZnO were synthesized, physicochemically characteriz...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698899/ https://www.ncbi.nlm.nih.gov/pubmed/36430396 http://dx.doi.org/10.3390/ijms232213918 |
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author | Jiménez-Holguín, Javier Arcos, Daniel Lozano, Daniel Saiz-Pardo, Melchor de Pablo, David Ortega, Luis Enciso, Silvia Fernández-Tomé, Blanca Díaz-Güemes, Idoia Sánchez-Margallo, Francisco Miguel Casarrubios, Laura Portolés, María Teresa Vallet-Regí, María |
author_facet | Jiménez-Holguín, Javier Arcos, Daniel Lozano, Daniel Saiz-Pardo, Melchor de Pablo, David Ortega, Luis Enciso, Silvia Fernández-Tomé, Blanca Díaz-Güemes, Idoia Sánchez-Margallo, Francisco Miguel Casarrubios, Laura Portolés, María Teresa Vallet-Regí, María |
author_sort | Jiménez-Holguín, Javier |
collection | PubMed |
description | Zinc-enriched mesoporous bioactive glasses (MBGs) are bioceramics with potential antibacterial and osteogenic properties. However, few assays have been performed to study these properties in animal models. In this study, MBGs enriched with up to 5% ZnO were synthesized, physicochemically characterized, and evaluated for their osteogenic activity both in vitro and in vivo. The ZnO MBGs showed excellent textural properties despite ZnO incorporation. However, the release of Zn(2+) ions inhibited the mineralization process when immersed in simulated body fluid. In vitro assays showed significantly higher values of viability and expression of early markers of cell differentiation and angiogenesis in a ZnO-content-dependent manner. The next step was to study the osteogenic potential in a sheep bone defect model. Despite their excellent textural properties and cellular response in vitro, the ZnO MBGs were not able to integrate into the bone tissue, which can be explained in terms of inhibition of the mineralization process caused by Zn(2+) ions. This work highlights the need to develop nanostructured materials for bone regeneration that can mineralize to interact with bone tissue and induce the processes of implant acceptance, cell colonization by osteogenic cells, and regeneration of lost bone tissue. |
format | Online Article Text |
id | pubmed-9698899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96988992022-11-26 In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model Jiménez-Holguín, Javier Arcos, Daniel Lozano, Daniel Saiz-Pardo, Melchor de Pablo, David Ortega, Luis Enciso, Silvia Fernández-Tomé, Blanca Díaz-Güemes, Idoia Sánchez-Margallo, Francisco Miguel Casarrubios, Laura Portolés, María Teresa Vallet-Regí, María Int J Mol Sci Article Zinc-enriched mesoporous bioactive glasses (MBGs) are bioceramics with potential antibacterial and osteogenic properties. However, few assays have been performed to study these properties in animal models. In this study, MBGs enriched with up to 5% ZnO were synthesized, physicochemically characterized, and evaluated for their osteogenic activity both in vitro and in vivo. The ZnO MBGs showed excellent textural properties despite ZnO incorporation. However, the release of Zn(2+) ions inhibited the mineralization process when immersed in simulated body fluid. In vitro assays showed significantly higher values of viability and expression of early markers of cell differentiation and angiogenesis in a ZnO-content-dependent manner. The next step was to study the osteogenic potential in a sheep bone defect model. Despite their excellent textural properties and cellular response in vitro, the ZnO MBGs were not able to integrate into the bone tissue, which can be explained in terms of inhibition of the mineralization process caused by Zn(2+) ions. This work highlights the need to develop nanostructured materials for bone regeneration that can mineralize to interact with bone tissue and induce the processes of implant acceptance, cell colonization by osteogenic cells, and regeneration of lost bone tissue. MDPI 2022-11-11 /pmc/articles/PMC9698899/ /pubmed/36430396 http://dx.doi.org/10.3390/ijms232213918 Text en © 2022 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 Jiménez-Holguín, Javier Arcos, Daniel Lozano, Daniel Saiz-Pardo, Melchor de Pablo, David Ortega, Luis Enciso, Silvia Fernández-Tomé, Blanca Díaz-Güemes, Idoia Sánchez-Margallo, Francisco Miguel Casarrubios, Laura Portolés, María Teresa Vallet-Regí, María In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model |
title | In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model |
title_full | In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model |
title_fullStr | In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model |
title_full_unstemmed | In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model |
title_short | In Vitro and In Vivo Response of Zinc-Containing Mesoporous Bioactive Glasses in a Sheep Animal Model |
title_sort | in vitro and in vivo response of zinc-containing mesoporous bioactive glasses in a sheep animal model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698899/ https://www.ncbi.nlm.nih.gov/pubmed/36430396 http://dx.doi.org/10.3390/ijms232213918 |
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