Impact of Biomimicry in the Design of Osteoinductive Bone Substitutes: Nanoscale Matters.
Animals
Biomimetic Materials
/ chemistry
Bone Regeneration
Bone Substitutes
/ chemistry
Bone and Bones
/ diagnostic imaging
Cell Adhesion
/ drug effects
Cell Differentiation
/ drug effects
Cells, Cultured
Dogs
Durapatite
/ chemistry
Mesenchymal Stem Cell Transplantation
Mesenchymal Stem Cells
/ cytology
Nanoparticles
/ chemistry
Osteoblasts
/ cytology
Osteocalcin
/ metabolism
Osteogenesis
/ drug effects
Rats
Tissue Scaffolds
/ chemistry
X-Ray Microtomography
biomimetic
calcium phosphate
carbonated apatite
foaming
nanostructure
osteogenesis
osteoinduction
Journal
ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991
Informations de publication
Date de publication:
06 Mar 2019
06 Mar 2019
Historique:
pubmed:
12
2
2019
medline:
15
6
2019
entrez:
12
2
2019
Statut:
ppublish
Résumé
Bone apatite consists of carbonated calcium-deficient hydroxyapatite (CDHA) nanocrystals. Biomimetic routes allow fabricating synthetic bone grafts that mimic biological apatite. In this work, we explored the role of two distinctive features of biomimetic apatites, namely, nanocrystal morphology (plate vs needle-like crystals) and carbonate content, on the bone regeneration potential of CDHA scaffolds in an in vivo canine model. Both ectopic bone formation and scaffold degradation were drastically affected by the nanocrystal morphology after intramuscular implantation. Fine-CDHA foams with needle-like nanocrystals, comparable in size to bone mineral, showed a markedly higher osteoinductive potential and a superior degradation than chemically identical coarse-CDHA foams with larger plate-shaped crystals. These findings correlated well with the superior bone-healing capacity showed by the fine-CDHA scaffolds when implanted intraosseously. Moreover, carbonate doping of CDHA, which resulted in small plate-shaped nanocrystals, accelerated both the intrinsic osteoinduction and the bone healing capacity, and significantly increased the cell-mediated resorption. These results suggest that tuning the chemical composition and the nanostructural features may allow the material to enter the physiological bone remodeling cycle, promoting a tight synchronization between scaffold degradation and bone formation.
Identifiants
pubmed: 30740968
doi: 10.1021/acsami.8b20749
doi:
Substances chimiques
Bone Substitutes
0
Osteocalcin
104982-03-8
Durapatite
91D9GV0Z28
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM