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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

Self-assembly of nanohydroxyapatite in mesoporous silica.

TL;DR: Variable crystallinity of HA involved in the mesopores yields from different sintering temperature, and correspondingly determines different degradation manners, which promises a high potential for application in drug and gene delivery.
Journal ArticleDOI

Mechanochemical Synthesis of SiO44–‐Substituted Hydroxyapatite, Part I – Kinetics of Interaction between the Components

TL;DR: In this paper, the kinetics of the room-temperature dry mechanochemical synthesis of hydroxyapatite modified by SiO44− ions have been studied for the first time.
Journal ArticleDOI

Crystal Structure Analysis of Si- and Zn-Codoped Tricalcium Phosphate by Neutron Powder Diffraction

TL;DR: In this article, the crystal structure of Si-Zn-codoped TCP (Si,Zn,Ca3(PO4)2) was studied by using a time-of-flight neutron powder diffraction and the Rietveld analysis method.
Journal ArticleDOI

Cation doped hydroxyapatite nanoparticles enhance strontium adsorption from aqueous system: a comparative study with and without calcination

TL;DR: In this paper, the synthesis of a biocompatible, eco-friendly, anisotropic cation doped hydroxyapatite nanoparticles (nHAp) for strontium removal from aqueous environment was reported.
Journal ArticleDOI

Systematic investigation and in vitro biocompatibility studies on mesoporous europium doped hydroxyapatite

TL;DR: Results confirmed the lack of toxicity and the biocompatibility of the Eu:HAp nanoparticles, Consequently, the possibility of using these nanoparticles for medical purposes without affecting the renal function can be envisaged.
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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