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Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects

Bone substitutes, like calcium phosphate, are implemented more frequently in orthopaedic surgery to reconstruct critical size defects, since autograft often results in donor site morbidity and allograft can transmit diseases. A novel bone cement, based on β-tricalcium phosphate, polyethylene glycol,...

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Autores principales: Bergmann, Christian J. D., Odekerken, Jim C. E., Welting, Tim J. M., Jungwirth, Franz, Devine, Declan, Bouré, Ludovic, Zeiter, Stephan, van Rhijn, Lodewijk W., Telle, Rainer, Fischer, Horst, Emans, Pieter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955683/
https://www.ncbi.nlm.nih.gov/pubmed/24719891
http://dx.doi.org/10.1155/2014/852610
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author Bergmann, Christian J. D.
Odekerken, Jim C. E.
Welting, Tim J. M.
Jungwirth, Franz
Devine, Declan
Bouré, Ludovic
Zeiter, Stephan
van Rhijn, Lodewijk W.
Telle, Rainer
Fischer, Horst
Emans, Pieter J.
author_facet Bergmann, Christian J. D.
Odekerken, Jim C. E.
Welting, Tim J. M.
Jungwirth, Franz
Devine, Declan
Bouré, Ludovic
Zeiter, Stephan
van Rhijn, Lodewijk W.
Telle, Rainer
Fischer, Horst
Emans, Pieter J.
author_sort Bergmann, Christian J. D.
collection PubMed
description Bone substitutes, like calcium phosphate, are implemented more frequently in orthopaedic surgery to reconstruct critical size defects, since autograft often results in donor site morbidity and allograft can transmit diseases. A novel bone cement, based on β-tricalcium phosphate, polyethylene glycol, and trisodium citrate, was developed to allow the rapid manufacturing of scaffolds, by extrusion freeform fabrication, at room temperature. The cement composition exhibits good resorption properties and serves as a basis for customised (e.g., drug or growth factor loaded) scaffolds for critical size bone defects. In vitro toxicity tests confirmed proliferation and differentiation of ATDC5 cells in scaffold-conditioned culture medium. Implantation of scaffolds in the iliac wing of sheep showed bone remodelling throughout the defects, outperforming the empty defects on both mineral volume and density present in the defect after 12 weeks. Both scaffolds outperformed the autograft filled defects on mineral density, while the mineral volume present in the scaffold treated defects was at least equal to the mineral volume present in the autograft treated defects. We conclude that the formulated bone cement composition is suitable for scaffold production at room temperature and that the established scaffold material can serve as a basis for future bone substitutes to enhance de novo bone formation in critical size defects.
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spelling pubmed-39556832014-04-09 Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects Bergmann, Christian J. D. Odekerken, Jim C. E. Welting, Tim J. M. Jungwirth, Franz Devine, Declan Bouré, Ludovic Zeiter, Stephan van Rhijn, Lodewijk W. Telle, Rainer Fischer, Horst Emans, Pieter J. Biomed Res Int Research Article Bone substitutes, like calcium phosphate, are implemented more frequently in orthopaedic surgery to reconstruct critical size defects, since autograft often results in donor site morbidity and allograft can transmit diseases. A novel bone cement, based on β-tricalcium phosphate, polyethylene glycol, and trisodium citrate, was developed to allow the rapid manufacturing of scaffolds, by extrusion freeform fabrication, at room temperature. The cement composition exhibits good resorption properties and serves as a basis for customised (e.g., drug or growth factor loaded) scaffolds for critical size bone defects. In vitro toxicity tests confirmed proliferation and differentiation of ATDC5 cells in scaffold-conditioned culture medium. Implantation of scaffolds in the iliac wing of sheep showed bone remodelling throughout the defects, outperforming the empty defects on both mineral volume and density present in the defect after 12 weeks. Both scaffolds outperformed the autograft filled defects on mineral density, while the mineral volume present in the scaffold treated defects was at least equal to the mineral volume present in the autograft treated defects. We conclude that the formulated bone cement composition is suitable for scaffold production at room temperature and that the established scaffold material can serve as a basis for future bone substitutes to enhance de novo bone formation in critical size defects. Hindawi Publishing Corporation 2014 2014-02-26 /pmc/articles/PMC3955683/ /pubmed/24719891 http://dx.doi.org/10.1155/2014/852610 Text en Copyright © 2014 Christian J. D. Bergmann et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bergmann, Christian J. D.
Odekerken, Jim C. E.
Welting, Tim J. M.
Jungwirth, Franz
Devine, Declan
Bouré, Ludovic
Zeiter, Stephan
van Rhijn, Lodewijk W.
Telle, Rainer
Fischer, Horst
Emans, Pieter J.
Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects
title Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects
title_full Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects
title_fullStr Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects
title_full_unstemmed Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects
title_short Calcium Phosphate Based Three-Dimensional Cold Plotted Bone Scaffolds for Critical Size Bone Defects
title_sort calcium phosphate based three-dimensional cold plotted bone scaffolds for critical size bone defects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955683/
https://www.ncbi.nlm.nih.gov/pubmed/24719891
http://dx.doi.org/10.1155/2014/852610
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