Fabrication of hydroxyapatite block from gypsum block based on (NH4)2HPO4 treatment

Dent Mater J. 2005 Dec;24(4):515-21. doi: 10.4012/dmj.24.515.

Abstract

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 degrees 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Substitutes / chemical synthesis*
  • Calcium Sulfate / chemistry
  • Durapatite / chemical synthesis*
  • Hydrogen-Ion Concentration
  • Microscopy, Electron, Scanning
  • Phosphates / chemistry
  • Quaternary Ammonium Compounds / chemistry
  • Spectroscopy, Fourier Transform Infrared
  • X-Ray Diffraction

Substances

  • Bone Substitutes
  • Phosphates
  • Quaternary Ammonium Compounds
  • ammonium phosphate
  • Durapatite
  • Calcium Sulfate