Highly porous polycaprolactone scaffolds doped with calcium silicate and dicalcium phosphate dihydrate designed for bone regeneration.
3T3 Cells
Animals
Bone Regeneration
/ drug effects
Calcium Compounds
/ pharmacology
Calcium Phosphates
/ pharmacology
Cell Proliferation
/ drug effects
Hydrogen-Ion Concentration
Mice
Polyesters
/ pharmacology
Porosity
Silicates
/ pharmacology
Spectrometry, X-Ray Emission
Spectrum Analysis, Raman
Temperature
Tissue Scaffolds
/ chemistry
X-Ray Diffraction
Bone regeneration
Calcium phosphate
Calcium silicate
Polycaprolactone
Porous scaffold
Thermally induced phase separation
Journal
Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
28
05
2018
revised:
31
01
2019
accepted:
12
04
2019
entrez:
1
6
2019
pubmed:
31
5
2019
medline:
21
11
2019
Statut:
ppublish
Résumé
Polycaprolactone (PCL), dicalcium phosphate dihydrate (DCPD) and/or calcium silicates (CaSi) have been used to prepare highly porous scaffolds by thermally induced phase separation technique (TIPS). Three experimental mineral-doped formulations were prepared (PCL-10CaSi, PCL-5CaSi-5DCPD, PCL-10CaSi-10DCPD); pure PCL scaffolds constituted the control group. Scaffolds were tested for their chemical-physical and biological properties, namely thermal properties by differential scanning calorimetry (DSC), mechanical properties by quasi-static parallel-plates compression testing, porosity by a standard water-absorption method calcium release, alkalinizing activity, surface microchemistry and micromorphology by Environmental Scanning electronic Microscopy (ESEM), apatite-forming ability in Hank Balanced Saline Solution (HBSS) by Energy Dispersive X-ray Spectroscopy (EDX) and micro-Raman, and direct contact cytotoxicity. All mineral-doped scaffolds released calcium and alkalinized the soaking medium, which may favor a good biological (osteogenic) response. ESEM surface micromorphology analyses after soaking in HBSS revealed: pure PCL, PCL-10CaSi and PCL-10CaSi-10DCPD kept similar surface porosity percentages but different pore shape modifications. PCL-5CaSi-5DCPD revealed a significant surface porosity increase despite calcium phosphates nucleation (p < 0.05). Micro-Raman spectroscopy detected the formation of a B-type carbonated apatite (Ap) layer on the surface of PCL-10CaSi-10DCPD aged for 28 days in HBSS; a similar phase (but of lower thickness) formed also on PCL-5CaSi-5DCPD and PCL; the deposit formed on PCL-10CaSi was mainly composed of calcite. All PCL showed bulk open porosity higher than 94%; however, no relevant brittleness was observed in the materials, which retained the possibility to be handled without collapsing. The thermo-mechanical properties showed that the reinforcing and nucleating action of the inorganic fillers CaSi and DCPD improved viscoelastic properties of the scaffolds, as confirmed by the increased value of storage modulus and the slight increase in the crystallization temperature for all the biomaterials. A detrimental effect on the mechanical properties was observed in samples with the highest amount of inorganic particles (PCL-10CaSi-10DCPD). All the scaffolds showed absence of toxicity, in particular PCL-10CaSi-10DCPD. The designed scaffolds are biointeractive (release biologically relevant ions), nucleate apatite, possess high surface and internal open porosity and can be colonized by cells, creating a bone forming osteoblastic microenvironment and appearing interesting materials for bone regeneration purposes.
Identifiants
pubmed: 31147007
pii: S0928-4931(18)31501-7
doi: 10.1016/j.msec.2019.04.040
pii:
doi:
Substances chimiques
Calcium Compounds
0
Calcium Phosphates
0
Polyesters
0
Silicates
0
polycaprolactone
24980-41-4
calcium phosphate, dibasic, dihydrate
O7TSZ97GEP
calcium silicate
S4255P4G5M
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
341-361Informations de copyright
Copyright © 2019. Published by Elsevier B.V.