Synthesis, characterization and thermal behavior of apatitic tricalcium phosphate

Synthetic calcium phosphate ceramic (CPC) surfaces can be transformed to a biological apatite through a sequence of reactions which include dissolution, precipitation, and ion exchange. By virtue of the reactions being material-dependent, it is important to determine parametric rate effects. In this study we focused on the effect of stoichiometry and crystal structure of CPCs on the dissolution kinetics. Monophase, biphase, and multiphase CPCs with a Ca/P ratio equal to or greater than 1.5 were studied. The experiments were performed in a calcium- and phosphate-free Tris buffer solution at pH 7.3. The dissolution behavior of the CPCs studied was found to vary over a wide range. The dissolution rate of the monophase CPCs increased in the order of stoichiometric hydroxyapatite, calcium deficient hydroxyapatite, oxyhydroxyapatite, beta-tricalcium phosphate, alpha-tricalcium phosphate, and tetracalcium phosphate. Dissolution of biphase and multiphase CPCs increased prorated the concentration of more soluble component.