Papers by Author: Luca Bertinetti

Abstract: Proper thermal treatments allowed to modify the number of surface Ca2+ able to coordinate water molecules on the surface of hydroxyapatite (HA) nanoparticles surrounded by an amorphous layer. Despite the consequent significant difference in the first hydration level between untreated and treated HA, the amount of adsorbed BSA, used as a model protein, remained essentially unchanged and the native structure of adsorbed protein was retained (as indicated by mid-IR ATR). Near-IR spectroscopy evidenced that adsorbed proteins should be in direct contact with surface Ca2+ through a displacement of H2O molecules by charged acidic residues. In agreement with a previous study that evidenced the heterogeneity of surface Ca2+ ions in terms of Lewis acidity, it was then proposed that the adsorption of BSA on such nano-HA should be ruled by some feature of the local structure of surface Ca2+ sites, prevailing on the total number of cationic sites exposed and the related features of the first hydration layer.

Abstract: The present work describes the development of biomimetic composites materials for bone tissue substitution and repair. At this purpose a biomimetic approach was used and apatitic phases were nucleated on macromolecular matrices like natural collagen, which act as template and induce peculiar physico-chemical features in the mineral phase.

Abstract: Hydroxyapatite powders characterized by substitutions of Mg2+, SiO4 4-, CO3 2- ions in biological like amounts, in the crystallographic site of calcium and phosphates, ions in biological like amounts, in the crystallographic site of calcium and phosphorus, were successfully prepared by synthesis in aqueous medium. The chemico-physical properties of the powders were investigated through several analytical techniques, among them: XRD, FTIR, TG-DTA, ICP-OES, HR-TEM. The entering of silicon in the HA structure progressively reduces its crystallinity, as also carbonate ions do. Silicate and carbonate ions can enter simultaneously into the HA structure, in biological-like amounts, although they compete for the occupation of the phosphate site. Solubility tests, carried out at physiological conditions, reveal an increased calcium release in the HA powders containing silicon compared to the silicon-free HA.

Abstract: In this work, we studied the surface/water interaction properties of a pure calcium hydroxyapatite (HA) and their modifications as a consequence of the partial Ca2+/Mg2+ (MHA) substitution by means of IR spectroscopy and microcalorimetry of adsorbed water. IR data indicated that water molecules in direct contact with the surface of HA are coordinated to surface cations and experience H-bond significantly stronger than in liquid water. The heats of adsorption associated to such interactions are very high, being twice-triple the heat of liquefaction of water. Interestingly, water experiences H-bond higher than in its bulk liquid state also in the second layer. Finally the entering in the material of Mg2+ ions was shown to significantly affect the affinity of the material toward water and the properties of its hydration layers.