In-vitro apatite layer formation on the surface of a newly developed glass reinforced hydroxyapatite composite was characterized using X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) equipped with energy dispersive X-ray analysis (EDXA). After I week soaking in an acellular simulated body fluid the composite surface was entirely covered by a Ca, P-layer, suggesting a bioactive behaviour. XPS binding energy results revealed that this surface layer was a carbonated and non-stoichiometric apatite with Ca/P ratio of 1.3. This apatite layer was composed of very fine needle-like crystallites. Comparative studies on a commercially available hydroxyapatite showed that a similar apatite layer was also formed on its surface.
Surface modifications of glass-reinforced hydroxyapatite composites immersed in a simulated physiological solution were studied using X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy.In the first stages of the apatite formation process, calcium and silicon ions were leached out from the surface of the composites. After 12 days of immersion, apatite crystals were detected on the surface indicating bioactive behaviour. Sodium ions attributed to sodium sulphate were also found in the apatite layer. Bound water on the surface also increased with immersion time.
P2O5-based glass hydroxyapatite (HA) composites denoted HA-2 oxide, HA-3 oxide, and HA-4-oxide, were immersed in Hank's balanced salt solution for a period of 1, 2, 3, and 4 weeks at 37 degrees C in nonagitated condition for in vitro evaluation. A surface layer was precipitated on the composites that was analyzed using scanning electron microscopy (SEM), X-ray photoelecton spectroscopy, and thin film X-ray diffractometry (TF-XRD). SEM micrographs showed complete coverage of the composite surface by crystallites after immersion of 1 week in the solution, which grew thicker with respect to immersion time. The binding energies measured by XPS indicated apatite formation and the presence of carbonate on the composite surface, showing the newly formed layer was a carbonated apatite. Confirmation of the formed apatite layer was obtained by TF-XRD.
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