Micro-/nano-structured scaffolds with a weight composition of 46.6% α-tricalcium phosphate (α-TCP)—53.4% silicocarnotite (SC) were synthesized by the polymer replica method. The scanning electron microscopy (SEM) analysis of the scaffolds and natural cancellous bone was performed for comparison purposes. Scaffolds were obtained at three cooling rates via the eutectoid temperature (50 °C/h, 16.5 °C/h, 5.5 °C/h), which allowed the surface nanostructure and mechanical strength to be controlled. Surface nanostructures were characterized by transmission electron microscopy (TEM) and Raman analysis. Both phases α-TCP and SC present in the scaffolds were well-identified, looked compact and dense, and had neither porosities nor cracks. The non-cytotoxic effect was evaluated in vitro by the proliferation ability of adult human mesenchymal stem cells (ah-MSCs) seeded on scaffold surfaces. There was no evidence for cytotoxicity and the number of cells increased with culture time. A dense cell-hydroxyapatite layer formed until 28 days. The SEM analysis suggested cell-mediated extracellular matrix formation. Finally, scaffolds were functionalized with the alkaline phosphatase enzyme (ALP) to achieve biological functionalization. The ALP was successfully grafted onto scaffolds, whose enzymatic activity was maintained. Scaffolds mimicked the micro-/nano-structure and chemical composition of natural cancellous bone by considering cell biology and biomolecule functionalization.
Biphasic scaffolds were prepared according to the eutectoid composition from subsystem silicocarnotite‐tricalcium phosphate by the polymeric replica method. Two polyurethane templates were used to explore the possibility of fabricating the scaffold on demand. The obtained scaffolds were characterized mineralogically by X‐Ray Diffraction (XRD), the chemical groups analyzed by Attenuated Total Reflectance‐Fourier Transformed Infrared Spectroscopy (ATR‐FTIR), microstructurally by Scanning Electron Microscopy (SEM) fitted with Energy Dispersive X‐Ray Spectroscopy (EDS), and additionally by field emission SEM (FESEM) for the topography study. Finally, the mercury porosimetry analysis was performed for the microporosity study. The obtained results confirmed the possibility of controlling macro‐ and microporosity on the scaffold, which allowed their synthesis for specific needs.
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