The structure of strontium-doped hydroxyapatite: an experimental and theoretical study

Abstract

First-principles modeling combined with experimental methods were used to study hydroxyapatite in which Sr²⁺ is substituted for Ca²⁺. Detailed analyses of cation–oxygen bond distributions, cation–cation distances, and site 1–oxygen polyhedron twist angles were made in order to provide an atomic-scale interpretation of the observed structural modifications. Density functional theory periodic band-structure calculations indicate that the Ca²⁺ to Sr²⁺ substitution induces strong local distortion on the hydroxyapatite lattice: the nearest neighbor Sr–O bond structures in both cationic sites are comparable to pure SrHA, while Sr induces more distortion at site 2 than site 1. Infrared vibrational spectroscopy (FTIR) and extended X-ray absorption fine structure (EXAFS) analysis suggest increasing lattice disorder and loss of OH with increasing Sr content. Rietveld refinement of synchrotron X-ray diffraction patterns shows a preference for the Ca1 site at Sr concentrations below 1 at.%. The ideal statistical occupancy ratio Sr2/Sr1 = 1.5 is achieved for ∼5 at.%; for higher Sr concentrations occupation of the Ca2 site is progressively preferred.