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Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release
Healing of large bone defects requires implants or scaffolds that provide structural guidance for cell growth, differentiation, and vascularization. In the present work, an agarose-hydroxyapatite composite scaffold was developed that acts not only as a 3D matrix, but also as a release system. Hydrox...
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/PMC6678963/ https://www.ncbi.nlm.nih.gov/pubmed/31330875 http://dx.doi.org/10.3390/ijms20143565 |
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author | Witzler, Markus Ottensmeyer, Patrick Frank Gericke, Martin Heinze, Thomas Tobiasch, Edda Schulze, Margit |
author_facet | Witzler, Markus Ottensmeyer, Patrick Frank Gericke, Martin Heinze, Thomas Tobiasch, Edda Schulze, Margit |
author_sort | Witzler, Markus |
collection | PubMed |
description | Healing of large bone defects requires implants or scaffolds that provide structural guidance for cell growth, differentiation, and vascularization. In the present work, an agarose-hydroxyapatite composite scaffold was developed that acts not only as a 3D matrix, but also as a release system. Hydroxyapatite (HA) was incorporated into the agarose gels in situ in various ratios by a simple procedure consisting of precipitation, cooling, washing, and drying. The resulting gels were characterized regarding composition, porosity, mechanical properties, and biocompatibility. A pure phase of carbonated HA was identified in the scaffolds, which had pore sizes of up to several hundred micrometers. Mechanical testing revealed elastic moduli of up to 2.8 MPa for lyophilized composites. MTT testing on Lw35human mesenchymal stem cells (hMSCs) and osteosarcoma MG-63 cells proved the biocompatibility of the scaffolds. Furthermore, scaffolds were loaded with model drug compounds for guided hMSC differentiation. Different release kinetic models were evaluated for adenosine 5′-triphosphate (ATP) and suramin, and data showed a sustained release behavior over four days. |
format | Online Article Text |
id | pubmed-6678963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66789632019-08-19 Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release Witzler, Markus Ottensmeyer, Patrick Frank Gericke, Martin Heinze, Thomas Tobiasch, Edda Schulze, Margit Int J Mol Sci Article Healing of large bone defects requires implants or scaffolds that provide structural guidance for cell growth, differentiation, and vascularization. In the present work, an agarose-hydroxyapatite composite scaffold was developed that acts not only as a 3D matrix, but also as a release system. Hydroxyapatite (HA) was incorporated into the agarose gels in situ in various ratios by a simple procedure consisting of precipitation, cooling, washing, and drying. The resulting gels were characterized regarding composition, porosity, mechanical properties, and biocompatibility. A pure phase of carbonated HA was identified in the scaffolds, which had pore sizes of up to several hundred micrometers. Mechanical testing revealed elastic moduli of up to 2.8 MPa for lyophilized composites. MTT testing on Lw35human mesenchymal stem cells (hMSCs) and osteosarcoma MG-63 cells proved the biocompatibility of the scaffolds. Furthermore, scaffolds were loaded with model drug compounds for guided hMSC differentiation. Different release kinetic models were evaluated for adenosine 5′-triphosphate (ATP) and suramin, and data showed a sustained release behavior over four days. MDPI 2019-07-21 /pmc/articles/PMC6678963/ /pubmed/31330875 http://dx.doi.org/10.3390/ijms20143565 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 Witzler, Markus Ottensmeyer, Patrick Frank Gericke, Martin Heinze, Thomas Tobiasch, Edda Schulze, Margit Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release |
title | Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release |
title_full | Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release |
title_fullStr | Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release |
title_full_unstemmed | Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release |
title_short | Non-Cytotoxic Agarose/Hydroxyapatite Composite Scaffolds for Drug Release |
title_sort | non-cytotoxic agarose/hydroxyapatite composite scaffolds for drug release |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678963/ https://www.ncbi.nlm.nih.gov/pubmed/31330875 http://dx.doi.org/10.3390/ijms20143565 |
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