Accelerated hardening of nanotextured 3D-plotted self-setting calcium phosphate inks
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29842972
DOI
10.1016/j.actbio.2018.05.042
PII: S1742-7061(18)30319-2
Knihovny.cz E-resources
- Keywords
- 3D plotting, Biomimetic, Bone graft, Bone regeneration, Calcium phosphate, Direct ink writing, Hydroxyapatite,
- MeSH
- Cell Adhesion MeSH
- Calcium Phosphates chemistry MeSH
- Ink * MeSH
- Rats MeSH
- Mesenchymal Stem Cells cytology metabolism MeSH
- Nanostructures chemistry MeSH
- Compressive Strength MeSH
- Polyethylenes chemistry MeSH
- Polypropylenes chemistry MeSH
- Rats, Inbred Lew MeSH
- Tissue Scaffolds chemistry MeSH
- Hot Temperature MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- alpha-tricalcium phosphate MeSH Browser
- Calcium Phosphates MeSH
- Polyethylenes MeSH
- Polypropylenes MeSH
- UCON 50-HB-5100 MeSH Browser
UNLABELLED: Direct ink writing (DIW) techniques open up new possibilities for the fabrication of patient-specific bone grafts. Self-setting calcium phosphate inks, which harden at low temperature, allow obtaining nanostructured scaffolds with biomimetic properties and enhanced bioactivity. However, the slow hardening kinetics hampers the translation to the clinics. Different hydrothermal treatments for the consolidation of DIW scaffolds fabricated with an α-tricalcium phosphate /pluronic F127 ink were explored, comparing them with a biomimetic treatment. Three different scaffold architectures were analysed. The hardening process, associated to the conversion of α-tricalcium phosphate to hydroxyapatite was drastically accelerated by the hydrothermal treatments, reducing the time for complete reaction from 7 days to 30 minutes, while preserving the scaffold architectural integrity and retaining the nanostructured features. β-tricalcium phosphate was formed as a secondary phase, and a change of morphology from plate-like to needle-like crystals in the hydroxyapatite phase was observed. The binder was largely released during the treatment. The hydrothermal treatment resulted in a 30% reduction of the compressive strength, associated to the residual presence of β-tricalcium phosphate. Biomimetic and hydrothermally treated scaffolds supported the adhesion and proliferation of rat mesenchymal stem cells, indicating a good suitability for bone tissue engineering applications. STATEMENT OF SIGNIFICANCE: 3D plotting has opened up new perspectives in the bone regeneration field allowing the customisation of synthetic bone grafts able to fit patient-specific bone defects. Moreover, this technique allows the control of the scaffolds' architecture and porosity. The present work introduces a new method to harden biomimetic hydroxyapatite 3D-plotted scaffolds which avoids high-temperature sintering. It has two main advantages: i) it is fast and simple, reducing the whole fabrication process from the several days required for the biomimetic processing to a few hours; and ii) it retains the nanostructured character of biomimetic hydroxyapatite and allows controlling the porosity from the nano- to the macroscale. Moreover, the good in vitro cytocompatibility results support its suitability for cell-based bone regeneration therapies.
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