The aim of this study was to evaluate the feasibility of fabricating low-crystalline, porous apatite block using set gypsum as a precursor based on the fact that apatite is thermodynamically more stable than gypsum. When the set gypsum was immersed in 1 mol/L diammonium hydrogen phosphate aqueous solution at 100°C, it transformed to low-crystalline porous apatite retaining its original shape. The transformation reaction caused a release of sulfate ions due to an ion exchange with phosphate ions, thus leading to a decrease in the pH of the solution. Then, due to decreased pH, dicalcium phosphate anhydrous - which has similar thermodynamic stability at lower pH - was also produced as a by-product. Apatite formed in the present method was low-crystalline, porous B-type carbonate apatite that contained approximately 0.5 wt % CO3, even though no carbonate sources - except carbon dioxide from air - were added to the reaction system. We concluded therefore that this is a useful bone filler fabrication method since B-type carbonate apatite is the biological apatite contained in bone.
CITATION STYLE
Suzuki, Y., Matsuya, S., Udoh, K. I., Nakagawa, M., Tsukiyama, Y., Koyano, K., & Ishikawa, K. (2005). Fabrication of hydroxyapatite block from gypsum block based on (NH 4)2HPO4 treatment. Dental Materials Journal, 24(4), 515–521. https://doi.org/10.4012/dmj.24.515
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