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Interface of synthetic inorganic biomaterials and bone regeneration
Interface of synthetic inorganic biomaterials and
bone regeneration
Osamu Suzuki*
Division of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry, Sendai, JapanAbstract. Synthetic inorganic calcium phosphate compounds have been utilized clinically to fill the
bone defect. Sintered hydroxyapatite (HA) and beta-tricalcium phosphate (h-TCP) bone substitutes
are known to be biocompatible and osteoconductive. Furthermore h-TCP is bioresorbable whereas
HA is not. Non-sintered synthetic octacalcium phosphate (OCP) has been shown to enhance bone
regeneration accompanied by the conversion into the hydrolyzed apatitic product in situ and the
biodegradation. There are still controversies over the chemical nature of the first mineral crystals
formed in bone, dentin, and cementum. However, OCP has been advocated to be a precursor of
biological apatite in these mineralized tissues because its existence could explain the non-
stoichiometry of the mineral crystals in their compositions. The surface of the implants as well as the
forming mineral crystals is continuously exposed to biological constituents, such as extracellular
matrices, inorganic biominerals, and cellular components. The conversion into the apatite from
inorganic precursor phases, such as OCP, could include a biomimetic process regarding the
interaction at the crystal surfaces in biological environments. It appears that the ideal artificial
scaffold to regenerate bone is resorbable, bioactive, and further activates host osteoprogenitor cells
by itself. The present paper focuses on the surface of synthetic inorganic biomaterials and bone
regeneration by synthetic precursors of HA, such as OCP, amorphous calcium phosphate (ACP) and
dicalcium phosphate (DCP). The analyses include mechanism of OCP hydrolysis into apatite,
experimentally stimulated bone formation by the implantation, and adsorption of biomolecules onto
the calcium phosphate compounds, of particular interest in reactive bone
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