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Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite
Modification of implantable scaffolds with magnesium and zinc for improvement of bone regeneration is a growing trend in the engineering of biomaterials. The aim of this study was to synthesize nano-hydroxyapatite substituted with magnesium (Mg(2+)) (HA-Mg) and zinc (Zn(2+)) (HA-Zn) ions in order to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695631/ https://www.ncbi.nlm.nih.gov/pubmed/31390753 http://dx.doi.org/10.3390/ijms20153835 |
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author | Kazimierczak, Paulina Kolmas, Joanna Przekora, Agata |
author_facet | Kazimierczak, Paulina Kolmas, Joanna Przekora, Agata |
author_sort | Kazimierczak, Paulina |
collection | PubMed |
description | Modification of implantable scaffolds with magnesium and zinc for improvement of bone regeneration is a growing trend in the engineering of biomaterials. The aim of this study was to synthesize nano-hydroxyapatite substituted with magnesium (Mg(2+)) (HA-Mg) and zinc (Zn(2+)) (HA-Zn) ions in order to fabricate chitosan-agarose-hydroxyapatite (HA) scaffolds (chit/aga/HA) with improved biocompatibility. Fabricated biomaterials containing Mg(2+) or Zn(2+) were tested using osteoblasts and mesenchymal stem cells to determine the effect of incorporated metal ions on cell adhesion, spreading, proliferation, and osteogenic differentiation. The study was conducted in direct contact with the scaffolds (cells were seeded onto the biomaterials) and using fluid extracts of the materials. It demonstrated that incorporation of Mg(2+) ions into chit/aga/HA structure increased spreading of the osteoblasts, promoted cell proliferation on the scaffold surface, and enhanced osteocalcin production by mesenchymal stem cells. Although biomaterial containing Zn(2+) did not improve cell proliferation, it did enhance type I collagen production by mesenchymal stem cells and extracellular matrix mineralization as compared to cells cultured in a polystyrene well. Nevertheless, scaffolds made of pure HA gave better results than material with Zn(2+). Results of the experiments clearly showed that modification of the chit/aga/HA scaffold with Zn(2+) did not have any positive impact on cell behavior, whereas, incorporation of Mg(2+) ions into its structure may significantly improve biocompatibility of the resultant material, increasing its potential in biomedical applications. |
format | Online Article Text |
id | pubmed-6695631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66956312019-09-05 Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite Kazimierczak, Paulina Kolmas, Joanna Przekora, Agata Int J Mol Sci Article Modification of implantable scaffolds with magnesium and zinc for improvement of bone regeneration is a growing trend in the engineering of biomaterials. The aim of this study was to synthesize nano-hydroxyapatite substituted with magnesium (Mg(2+)) (HA-Mg) and zinc (Zn(2+)) (HA-Zn) ions in order to fabricate chitosan-agarose-hydroxyapatite (HA) scaffolds (chit/aga/HA) with improved biocompatibility. Fabricated biomaterials containing Mg(2+) or Zn(2+) were tested using osteoblasts and mesenchymal stem cells to determine the effect of incorporated metal ions on cell adhesion, spreading, proliferation, and osteogenic differentiation. The study was conducted in direct contact with the scaffolds (cells were seeded onto the biomaterials) and using fluid extracts of the materials. It demonstrated that incorporation of Mg(2+) ions into chit/aga/HA structure increased spreading of the osteoblasts, promoted cell proliferation on the scaffold surface, and enhanced osteocalcin production by mesenchymal stem cells. Although biomaterial containing Zn(2+) did not improve cell proliferation, it did enhance type I collagen production by mesenchymal stem cells and extracellular matrix mineralization as compared to cells cultured in a polystyrene well. Nevertheless, scaffolds made of pure HA gave better results than material with Zn(2+). Results of the experiments clearly showed that modification of the chit/aga/HA scaffold with Zn(2+) did not have any positive impact on cell behavior, whereas, incorporation of Mg(2+) ions into its structure may significantly improve biocompatibility of the resultant material, increasing its potential in biomedical applications. MDPI 2019-08-06 /pmc/articles/PMC6695631/ /pubmed/31390753 http://dx.doi.org/10.3390/ijms20153835 Text en © 2019 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 Kazimierczak, Paulina Kolmas, Joanna Przekora, Agata Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite |
title | Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite |
title_full | Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite |
title_fullStr | Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite |
title_full_unstemmed | Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite |
title_short | Biological Response to Macroporous Chitosan-Agarose Bone Scaffolds Comprising Mg- and Zn-Doped Nano-Hydroxyapatite |
title_sort | biological response to macroporous chitosan-agarose bone scaffolds comprising mg- and zn-doped nano-hydroxyapatite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695631/ https://www.ncbi.nlm.nih.gov/pubmed/31390753 http://dx.doi.org/10.3390/ijms20153835 |
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