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Journal ArticleDOI

Chemical characterization of silicon-substituted hydroxyapatite.

TLDR
Chemical analysis confirmed the proposed substitution of the silicon (or silicate) ion for the phosphorus (or phosphate) ion in hydroxyapatite and demonstrated that phase-pure silicon-substituted hydroxyAPatite may be prepared using a simple precipitation technique.
Abstract
Bioceramic specimens have been prepared by incorporating a small amount of silicon (0.4 wt %) into the structure of hydroxyapatite [Ca10(PO4)6(OH)2, HA] via an aqueous precipitation reaction to produce a silicon-substituted hydroxyapatite (Si-HA). The results of chemical analysis confirmed the proposed substitution of the silicon (or silicate) ion for the phosphorus (or phosphate) ion in hydroxyapatite. The Si-HA was produced by first preparing a silicon-substituted apatite (Si-Ap) by a precipitation process. A single-phase Si-HA was obtained by heating/calcining the as-prepared Si-Ap to temperatures above 700 degrees C; no secondary phases, such as tricalcium phosphate (TCP), tetracalcium phosphate (TeCP), or calcium oxide (CaO), were observed by X-ray diffraction analysis. Although the X-ray diffraction patterns of Si-HA and stoichiometric HA appeared to be identical, refinement of the diffraction data revealed some small structural differences between the two materials. The silicon substitution in the HA lattice resulted in a small decrease in the a axis and an increase in the c axis of the unit cell. This substitution also caused a decrease in the number of hydroxyl (OH) groups in the unit cell, which was expected from the proposed substitution mechanism. The incorporation of silicon in the HA lattice resulted in an increase in the distortion of the PO4 tetrahedra, indicated by an increase in the distortion index. Analysis of the Si-HA by Fourier transform infrared (FTIR) spectroscopy indicated that although the amount of silicon incorporated into the HA lattice was small, silicon substitution appeared to affect the FTIR spectra of HA, in particular the P-O vibrational bands. The results demonstrate that phase-pure silicon-substituted hydroxyapatite may be prepared using a simple precipitation technique.

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Citations
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Journal ArticleDOI

Total attenuated reflection infrared analysis of silicon-stabilized tri-calcium phosphate.

TL;DR: Increased resolution allows the study of weak bands linked to Si at 668, 800, 863, and 892 cm(-1) and suggests that the loss of PO(4)(3-) coincides with the development of different silicate groups-SiO(4) at lower doping levels and a new silicon species at higher doping.
Journal ArticleDOI

Microstructure and chemistry affects apatite nucleation on calcium phosphate bone graft substitutes

TL;DR: Results indicate that strut-porosity of a material affects the potential for formation of a precursor to bone-like apatite and further confirms previous findings that β-tricalcium phosphate is less bioactive than hydroxyapatite.
Journal ArticleDOI

Phase transitions in single phase Si–Ca–P-based ceramic under thermal treatment

TL;DR: In this article, the influence of thermal treatment on phase transformations of Si-Ca-P (Nurse's A ss ) single phase ceramic was investigated and the results showed that the phase evolution during the synthesis of ceramic was influenced by the type of raw materials used while annealing within the 1000-1500°C range for 2h, the interdiffusion of silica and phosphorous took place.
Journal ArticleDOI

Interfacial study of magnesium-containing fluoridated hydroxyapatite coatings

TL;DR: Magnesium-containing fluoridated hydroxyapatite (MgxFHA) coatings have been developed to improve the biological performances of FHA coatings.
Journal ArticleDOI

Si complexes in calcium phosphate biomaterials

TL;DR: NMR results showed that in all three materials the silicon dopants formed Q1 structures in which two silicate tetrahedra share an oxygen, creating an oxygen vacancy which compensated the substitution of two silicon for phosphorus, may explain the phase evolution previously found where silicon stabilized α-TCP is found at low temperature after sintering.
References
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Journal ArticleDOI

Bioceramics: From Concept to Clinic

TL;DR: The mechanisms of tissue bonding to bioactive ceramics are beginning to be understood, which can result in the molecular design of bioceramics for interfacial bonding with hard and soft tissues.
Journal Article

Bioceramics : from concept to clinic

TL;DR: The mechanisms of tissue bonding to bioactive ceramics are beginning to be understood, which can result in the molecular design of bioceramics for interfacial bonding with hard and soft tissues.
Journal ArticleDOI

Silicon: A Possible Factor in Bone Calcification

TL;DR: Silicon, a relatively unknown trace element in nutritional research, has been uniquely localized in active calcification sites in young bone and is suggested to be associated with calcium in an early stage of calcification.
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