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Barba, A. Maazouz, Y. Diez-Escudero, A. Rappe, K. Espanol, M. Montufar, EB. Ohman-Magi, C. Persson, C. Fontecha, P. Manzanares, MC. Franch, J. Ginebra, MP.
Original Title
Osteogenesis by foamed and 3D-printed nanostructured calcium phosphate scaffolds: Effect of pore architecture
Type
journal article in Web of Science
Language
English
Original Abstract
There is an urgent need of synthetic bone grafts with enhanced osteogenic capacity. This can be achieved by combining biomaterials with exogenous growth factors, which however can have numerous undesired side effects, but also by tuning the intrinsic biomaterial properties. In a previous study, we showed the synergistic effect of nanostructure and pore architecture of biomimetic calcium deficient hydroxyapatite (CDHA) scaffolds in enhancing osteoinduction, i.e. fostering the differentiation of mesenchymal stem cells to bone forming cells. This was demonstrated by assessing bone formation after implanting the scaffolds intramuscularly. The present study goes one step forward, since it analyzes the effect of the geometrical features of the same CDHA scaffolds, obtained either by 3D-printing or by foaming, on the osteogenic potential and resorption behaviour in a bony environment. After 6 and 12 weeks of intraosseous implantation, both bone formation and material degradation had been drastically affected by the macropore architecture of the scaffolds. Whereas nanostructured CDHA was shown to be highly osteoconductive both in the robocast and foamed scaffolds, a superior osteogenic capacity was observed in the foamed scaffolds, which was associated with their higher intrinsic osteoinductive potential. Moreover, they showed a significantly higher cell-mediated degradation than the robocast constructs, with a simultaneous and progressive replacement of the scaffold by new bone. In conclusion, these results demonstrate that the control of macropore architecture is a crucial parameter in the design of synthetic bone grafts, which allows fostering both material degradation and new bone formation. Statement of Significance 3D-printing technologies open new perspectives for the design of patient-specific bone grafts, since they allow customizing the external shape together with the internal architecture of implants. In this respect, it is important to design the appropriate pore geometry to maximize the bone healing capacity of these implants. The present study analyses the effect of pore architecture of nanostructured hydroxyapatite scaffolds, obtained either by 3D-printing or foaming, on the osteogenic potential and scaffold resorption in an in vivo model. While nanostructured hydroxyapatite showed excellent osteoconductive properties irrespective of pore geometry, we demonstrated that the spherical, concave macropores of foamed scaffolds significantly promoted both material resorption and bone regeneration compared to the 3D-printed scaffolds with orthogonal-patterned struts and therefore prismatic, convex macropores. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
Keywords
Osteogenesis; Pore architecture; 3D-printing; Foaming; Calcium phosphate
Authors
Barba, A.; Maazouz, Y.; Diez-Escudero, A.; Rappe, K.; Espanol, M.; Montufar, EB.; Ohman-Magi, C.; Persson, C.; Fontecha, P.; Manzanares, MC.; Franch, J. Ginebra, MP.
Released
1. 10. 2018
Publisher
ELSEVIER SCI LTD
Location
OXFORD
ISBN
1742-7061
Periodical
Acta Biomaterialia
Year of study
79
Number
1
State
United Kingdom of Great Britain and Northern Ireland
Pages from
135
Pages to
147
Pages count
13
URL
https://www.sciencedirect.com/science/article/pii/S1742706118305208
BibTex
@article{BUT163366, author="Barba, A. and Maazouz, Y. and Diez-Escudero, A. and Rappe, K. and Espanol, M. and Montufar, EB. and Ohman-Magi, C. and Persson, C. and Fontecha, P. and Manzanares, MC. and Franch, J. Ginebra, MP.", title="Osteogenesis by foamed and 3D-printed nanostructured calcium phosphate scaffolds: Effect of pore architecture", journal="Acta Biomaterialia", year="2018", volume="79", number="1", pages="135--147", doi="10.1016/j.actbio.2018.09.003", issn="1742-7061", url="https://www.sciencedirect.com/science/article/pii/S1742706118305208" }