The silicate-based bioactive glass S53P4 is clinically used in bone regenerative applications in granule form. However, utilization of the glass in scaffold form has been limited by the high tendency of the glass to crystallize during sintering. Here, careful optimization of sintering parameters enabled the manufacture of porous amorphous S53P4 scaffolds with a strength high enough for surgical procedures in bone applications (5 MPa). Sintering was conducted in a laboratory furnace for times ranging from 25 to 300 min at 630 °C, i.e., narrowly below the commencement of the crystallization. The phase composition of the scaffolds was verified with XRD, and the ion release was tested in vitro and compared with granules in continuous flow of Tris buffer and simulated body fluid (SBF). The amorphous, porous S53P4 scaffolds present the possibility of using the glass composition in a wider range of applications.
Static and dynamic in vitro dissolution studies showed large differences for various size-fractions of non-porous, flame-sprayed commercial microspheres (45-500 µm) of bioactive glass S53P4.The smaller the spheres, the more their composition deviated from the nominal glass. The dissolution studies were carried out in simulated body fluid and tris(hydroxymethyl) aminomethane buffer for seven days. The ion concentrations in solutions were analyzed using inductively coupled plasma optical emission spectrometry, and the pH was measured as a function of time. Also, changes in the sphere size distribution and mass losses were determined. The calcium phosphate and the silica-rich layers at the sphere surfaces were investigated using scanning electron microscopy after several immersion times. The smallest (45-90 µm) spheres appeared almost inert. In contrast, typical silica-rich and calcium phosphate layers were identified at the largest spheres after three days of static and dynamic dissolutions. During the past years, bioactive glass microspheres have been added to paste-like injectable bone grafting materials, putties to enhance their molding properties. The obtained results provide a better understanding of the dissolution patterns of bioactive glass microspheres.
Sodium-calcium-phosphate based oxynitride glasses and glass-ceramics doped with Mg, Si, and Nb were studied in vitro in simulated body fluid (SBF) under static conditions. The release of ions and pH changes up to 7 days of immersion were investigated. The nitrogen incorporation into phosphate glass matrix was found to notably influence in vitro dissolution only of homogenous glasses. Increasing the nitrogen content in the samples decreased the mean mass loss, while the niobate incorporation increased it. The correlation between the nitrogen content and increase in pH of SBF was also observed. The presence of phosphates crystallites was found to support the dissolution process at the beginning step (up to 3 days).
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