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In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications

In addition to good mechanical properties needed for three-dimensional tissue engineering, the combination of alginate dialdehyde, gelatin and nano-scaled bioactive glass (45S5) is supposed to combine excellent cellular adhesion, proliferation and differentiation properties, good biocompatibility an...

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Autores principales: Rottensteiner, Ulrike, Sarker, Bapi, Heusinger, Dominik, Dafinova, Diana, Rath, Subha N., Beier, Justus P., Kneser, Ulrich, Horch, Raymund E., Detsch, Rainer, Boccaccini, Aldo R., Arkudas, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453292/
https://www.ncbi.nlm.nih.gov/pubmed/28788549
http://dx.doi.org/10.3390/ma7031957
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author Rottensteiner, Ulrike
Sarker, Bapi
Heusinger, Dominik
Dafinova, Diana
Rath, Subha N.
Beier, Justus P.
Kneser, Ulrich
Horch, Raymund E.
Detsch, Rainer
Boccaccini, Aldo R.
Arkudas, Andreas
author_facet Rottensteiner, Ulrike
Sarker, Bapi
Heusinger, Dominik
Dafinova, Diana
Rath, Subha N.
Beier, Justus P.
Kneser, Ulrich
Horch, Raymund E.
Detsch, Rainer
Boccaccini, Aldo R.
Arkudas, Andreas
author_sort Rottensteiner, Ulrike
collection PubMed
description In addition to good mechanical properties needed for three-dimensional tissue engineering, the combination of alginate dialdehyde, gelatin and nano-scaled bioactive glass (45S5) is supposed to combine excellent cellular adhesion, proliferation and differentiation properties, good biocompatibility and predictable degradation rates. The goal of this study was to evaluate thein vitro and in vivo biocompatibility as a first step on the way to its use as a scaffold in bone tissue engineering. In vitro evaluation showed good cell adherence and proliferation of bone marrow derived mesenchymal stem cells seeded on covalently crosslinked alginate dialdehyde-gelatin (ADA-GEL) hydrogel films with and without 0.1% nano-Bioglass(®)(nBG). Lactate dehydrogenase (LDH)- and mitochondrial activity significantly increased in both ADA-GEL and ADA-GEL-nBG groups compared to alginate. However, addition of 0.1% nBG seemed to have slight cytotoxic effect compared to ADA-GEL. In vivo implantation did not produce a significant inflammatory reaction, and ongoing degradation could be seen after four weeks. Ongoing vascularization was detected after four weeks. The good biocompatibility encourages future studies using ADA-GEL and nBG for bone tissue engineering application.
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spelling pubmed-54532922017-07-28 In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications Rottensteiner, Ulrike Sarker, Bapi Heusinger, Dominik Dafinova, Diana Rath, Subha N. Beier, Justus P. Kneser, Ulrich Horch, Raymund E. Detsch, Rainer Boccaccini, Aldo R. Arkudas, Andreas Materials (Basel) Article In addition to good mechanical properties needed for three-dimensional tissue engineering, the combination of alginate dialdehyde, gelatin and nano-scaled bioactive glass (45S5) is supposed to combine excellent cellular adhesion, proliferation and differentiation properties, good biocompatibility and predictable degradation rates. The goal of this study was to evaluate thein vitro and in vivo biocompatibility as a first step on the way to its use as a scaffold in bone tissue engineering. In vitro evaluation showed good cell adherence and proliferation of bone marrow derived mesenchymal stem cells seeded on covalently crosslinked alginate dialdehyde-gelatin (ADA-GEL) hydrogel films with and without 0.1% nano-Bioglass(®)(nBG). Lactate dehydrogenase (LDH)- and mitochondrial activity significantly increased in both ADA-GEL and ADA-GEL-nBG groups compared to alginate. However, addition of 0.1% nBG seemed to have slight cytotoxic effect compared to ADA-GEL. In vivo implantation did not produce a significant inflammatory reaction, and ongoing degradation could be seen after four weeks. Ongoing vascularization was detected after four weeks. The good biocompatibility encourages future studies using ADA-GEL and nBG for bone tissue engineering application. MDPI 2014-03-06 /pmc/articles/PMC5453292/ /pubmed/28788549 http://dx.doi.org/10.3390/ma7031957 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Rottensteiner, Ulrike
Sarker, Bapi
Heusinger, Dominik
Dafinova, Diana
Rath, Subha N.
Beier, Justus P.
Kneser, Ulrich
Horch, Raymund E.
Detsch, Rainer
Boccaccini, Aldo R.
Arkudas, Andreas
In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications
title In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications
title_full In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications
title_fullStr In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications
title_full_unstemmed In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications
title_short In vitro and in vivo Biocompatibility of Alginate Dialdehyde/Gelatin Hydrogels with and without Nanoscaled Bioactive Glass for Bone Tissue Engineering Applications
title_sort in vitro and in vivo biocompatibility of alginate dialdehyde/gelatin hydrogels with and without nanoscaled bioactive glass for bone tissue engineering applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453292/
https://www.ncbi.nlm.nih.gov/pubmed/28788549
http://dx.doi.org/10.3390/ma7031957
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