Abstract
The present study investigates the influence of the substitution of CaO by SrO on the structure, degradation and in vitro apatite formation of sol–gel-derived bioactive glasses with composition of 58SiO2–(38-x)CaO–xSrO–4P2O5, where x varies between 0 and 10 mol.%. The IV-type nitrogen adsorption/desorption isotherms and pore size values (ranging from 5.41 to 12.56 nm) confirmed the mesoporous structure of the synthesized glasses. The detailed structural analysis was carried out by X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and Fourier transform infrared spectroscopy (FTIR). As network modifiers, the addition of Ca and Sr oxides disrupted the bonds of bridging oxygens (BOs) and resulted in the formation of non-bridging oxygens (NBOs), where the substitution of Ca with Sr led to an increase in Q1 units and a decrease in Q3 units. The effects of the addition of Sr on sample degradation and apatite formation were assessed using an assay in tris-(hydroxymethyl)-aminomethane and hydrochloric acid (Tris–HCl) and simulated body fluid (SBF). The results demonstrated that the substitution of CaO by SrO in the CaO–SiO2–P2O5 bioglass system altered the glass structure, resulting in reduced sample degradation and delayed apatite formation. This suggests that the incorporation of Sr into bioactive glasses may serve as a promising strategy to regulate the structure, dissolution behavior and apatite formation of silicate-based glasses, particularly concerning their long-term applications within the human body.
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