Mechanical and Biological Properties of Magnesium- and Silicon-Substituted Hydroxyapatite Scaffolds.
Sanosh Kunjalukkal PadmanabhanPaola NittiEleonora StancaAlessio RochiraLuisa SiculellaMaria Grazia RaucciMarta MadaghieleAntonio LicciulliChristian DemitriPublished in: Materials (Basel, Switzerland) (2021)
Magnesium (Mg)- and silicon (Si)-substituted hydroxyapatite (HA) scaffolds were synthesized using the sponge replica method. The influence of Mg2+ and SiO44- ion substitution on the microstructural, mechanical and biological properties of HA scaffolds was evaluated. All synthesized scaffolds exhibited porosity >92%, with interconnected pores and pore sizes ranging between 200 and 800 μm. X-ray diffraction analysis showed that β-TCP was formed in the case of Mg substitution. X-ray fluorescence mapping showed a homogeneous distribution of Mg and Si ions in the respective scaffolds. Compared to the pure HA scaffold, a reduced grain size was observed in the Mg- and Si-substituted scaffolds, which greatly influenced the mechanical properties of the scaffolds. Mechanical tests revealed better performance in HA-Mg (0.44 ± 0.05 MPa), HA-Si (0.64 ± 0.02 MPa) and HA-MgSi (0.53 ± 0.01 MPa) samples compared to pure HA (0.2 ± 0.01 MPa). During biodegradability tests in Tris-HCl, slight weight loss and a substantial reduction in mechanical performances of the scaffolds were observed. Cell proliferation determined by the MTT assay using hBMSC showed that all scaffolds were biocompatible, and the HA-MgSi scaffold seemed the most effective for cell adhesion and proliferation. Furthermore, ALP activity and osteogenic marker expression analysis revealed the ability of HA-Si and HA-MgSi scaffolds to promote osteoblast differentiation.
Keyphrases
- tissue engineering
- cell proliferation
- weight loss
- molecular docking
- high resolution
- room temperature
- magnetic resonance imaging
- multiple sclerosis
- computed tomography
- mesenchymal stem cells
- signaling pathway
- bariatric surgery
- quantum dots
- molecular dynamics
- molecular dynamics simulations
- body mass index
- cell cycle
- white matter
- ionic liquid