Effect of Fluoride on the Ion-association of Calcium Phosphate and Crystallization of Hydroxyapatite

Using a titration setup to accurately control the reaction conditions and in situ monitor the reaction,we showed that fluoride exhibited negligible effects on the ion association process of calcium and phosphate and the formation of ACP nanospheres in a buffer solution with constant ionic strength.However,the stability of ACP increased with increasing fluoride concentration,which was ascribed to the inhibitory effect of fluoride on the aggregation of ACP nanospheres and the nucleation of nanocrystals on the surface of ACP nanospheres.Furthermore,fluoride could inhibit the lateral growth of HAP nanosheets and promote the formation of rod-like crystals.These results further improve our understanding of the crystallization pathway of HAP crystals and the regulatory effects of fluoride.

Characterization of Hydroxyapatite Extracted from Crab Shell Using the Hydrothermal Method with Varying Holding Times

Hydroxyapatite(HA)is a bio ceramic commonly utilized in bone tissue engineering due to its bioactive and osteoconductive properties.Crab shells are usually disregarded as waste material despite their significant CaCO_(3) content,and have not been widely utilized in the synthesis of HA.This study aims to synthesize and analyze HA derived from crab shells using the hydrothermal method with different durations of holding time.This study utilized precipitated calcium carbonate(PCC)derived from crab shells.With a hydrothermal reactor set at 160℃ and varying holding times of 14(HA_14),16(HA_16),and 18(HA_18)h,a PCC and(NH4)2HPO4 mixture was used to synthesize HA.The synthesis results were analyzed using scanning electron microscopy(SEM),fourier transform infrared spectroscopy(FTIR),and X-ray diffraction(XRD)tests.This study has accomplished the synthesis of HA from crab shells.Nonetheless,the final product of synthesis still contained CaCO_(3) as an impurity.The prolonged hydrothermal holding time of 14 to 18 h resulted in a reduction of impurities while increasing the percentage of crystal weight and crystallite size of HA.Specimen CH_18 is the best-quality product generated in this study.This specimen produced HA with the highest percentage of crystal weight and crystallite size compared to the other specimens.Furthermore,specimen CH_18 exhibited the lowest concentration of impurities.The Ca/P ratio in this specimen was also the closest to 1.67.The Ca/P ratio,crystallite size,and crystal weight percentage of this specimen are 1.54,19.06 nm,and 99.1%,respectively.

Synthesis of Crystalline Hydroxyapatite from CaCO_3 and CaHPO_4·2H_2O by Mechanochemical Method

The mixture of CaHPO 4·2H 2O and CaCO 3 was ground in an aqueous system under appropriate conditions to investigate the mechanochemical reaction for the synthesis of crystalline hydroxyapatite (HA) powder. Hydroxyapatite of high crystallinity powder including trace Ca 10 (PO 4) 6CO 3(OH) and Ca 9HPO 4(PO 4) 6OH can be synthesized by mechanical activation without further thermal treatment at a high temperature. The synthesis reaction during the grinding process was almost completed within 1h. The as-ground powder exhibits a particle distribution of 20-100nm in size with a spherical or rodlike morphology. The composition and degree of crystallinity of the mechanochemical synthesized hydroxyapatite powders were coincident with the cement-type hydroxyapatite.

Synthesis and characterization of arginine-modified and europium-doped hydroxyapatite nanoparticle and its cell viability

The arginine-modified and europium-doped hydroxyapatite nanoparticles（HAP-Eu） were synthesized by hydrothermal synthesis.The prepared nanoparticles were characterized by transmission electron microscopy（TEM）,X-ray diffractometry（XRD）,Fourier transform infrared（FTIR） and zeta potential analyzer.The cell viability of HAP-Eu was tested by image flow cytometry.The results indicated that HAP-Eu is short column shapes and its size is approximately 100 nm,its zeta potential is about 30.10 mV at pH of 7.5,and shows no cytotoxicity in human epithelial cells and endothelial cells.

Cytotoxinic Mechanism of Hydroxyapatite Nanoparticles on Human Hepatoma Cell Lines

Stable and single dispersed HAP nanoparticles were synthesized with chemical method assisted by ultrasonic treatment.HAP nanoparticles were surveyed by AFM and Zataplus.The effect on the Bel-7402 human hepatoma cell lines treated with HAP nanoparticles was investigated by the MTT methods and observation of morphology,and the mechanism was studied in changes of cell cycle and ultrastructure.The result shows that inhibition of HAP nanoparticles on the Bel 7402 human hepatoma cell lines is obviously in vitro.HAP nanoparticles the entered cancer cytoplasm,and cell proliferation is stopped at G 1 phase of cell cycle,thus,cancer cells die directly.

Hot pressing of hydroxyapatite(HA)-Ti material and stability of HA

Hot pressing of hydroxyapatite(HA) Ti system material and the stability of HA component were investigated to supply the foundation of optimizing sintering procedure of HA Ti functionally graded material(FGM). The results show that the HA powders used have excellent thermal stability and no decomposition is observed at 1 300 ℃. The existence of Ti can promote the dehydration and decomposition of HA. However, no new compounds form between HA and Ti. By selecting sintering parameters properly, ideal HA Ti material can be acquired. The relative densities of the mixtures of HA and Ti are always lower than those of pure HA or Ti, which may be caused by the decomposition of HA in the mixtures.

Preparation, Characterization and Antibacterial Property of Cerium Substituted Hydroxyapatite Nanoparticles

Nanoparticles of hydroxyapatite （HAP） and cerium substituted hydroxyapatite （CeHAP） with the atomic ratio of Ce/[ Ca ＋ Ce] （xco） from 0 to 0.2 were prepared by sol-gel-supercritical fluid drying （SCFD） method. The nanoparticles were characterized by TEM, XRD, and FT-IR, and the effects of cerium on crystal structure, crystallinity, and particle shape were discussed. With the tests of bacterial inhibition zone and antibacterial ratio, the antibacterial property of HAP and CeHAP nanoparticles on Escherichia coli, Staphylococcus aureus, Lactobacillus were researched. Results showed that the nanoparticles of HAP and CeHAP could be made by sol-gel-SCFD, cerium could partially substitute for calcium and enter the structure of HAP. After substitution, the crystallinity, the IR wavenumbers of bonds in CeHAP decreased gradually with increase of cerium substitution, and the morphology of the nanoparticles changed from the short rod-shaped HAP to the needle-shaped CeHAP. The nanoparticles of HAP and CeHAP with Xco below 0.08 had antibacterial property only forcibly contacting with the test bacteria at the test concentration of 0.1 g · mi^-1, however, the Ce- HAP nanoparticles had antibacterial ability at that concentration no matter statically or dynamically contacting with the test bacteria when Xco was above 0.08, and the antibacterial ability gets better with the increase Of Xce, indicating that the antibacterial property was improved after calcium was partially substituted by cerium. The improved antibacterial effects of CeHAP nanoparticle on Lactobacillus showed its potential ability to anticaries.

Morphology and Phase Compositions of Hydroxyapatite Powder Particles Plasma-sprayed into Water

Hydroxyapatite powder particles were plasma sprayed into water, their inner structures and phase compositions were studied by using scanning electron microscope(SEM) and X-ray diffractometer. The results show that the molten HA particles have a central hollow morphology and high crystallinity. The hollow morphology was caused by sublimated P2O5 and H2O, which will have an effect on surface morphology, cohesive and adhesive strength as well as dissolution and degradation of coating. The high crystallinity is attributed to lower cooling speed in water.

Synthesis,Characterization and Antibacterial Property of Strontium Half and Totally Substituted Hydroxyapatite Nanoparticles

Nanoparticles of hydroxyapatite（HAP）, strontium half substituted hydroxyapatite （SrCaHAP） and strontium totally substituted hydroxyapatite （SrHAP） were prepared by sol-gel-supercritical fluid drying （SCFD） method. The nanoparticles were characterized by element content analysis, FT-IR, XRD and TEM, and the effects of strontium substitution on crystal structure, crystallinity, particle shape and antibacterial properties of the nanoparticles on Escherichia coli, Staphylococcus aureus, Lactobacillus were researched. Results show that strontium can half and totally substitute for calcium and enter the structure of apatite according to the initial atomic ratios of Sr/[Sr＋Ca] as 0.5, 1. The substitution decreases the IR wavenumbers of SrCaHAP and SrHAP, and changes the morphology of the nanoparticles from short rod shaped HAP to needle shaped SrCaHAP, and back to short rod shaped SrHAP. The crystallinity of HAP is higher than that of SrCaHAP, but is lower than that of SrHAP. Moreover, the antibacterial property of SrCaHAP and SrHAP are improved after the calcium is half and totally substituted by strontium.

Synthesis and Characterization of Core-shell Hydroxyapatite/chitosan Biocomposite Nanospheres

Novel core-shell hydroxyapatite/chitosan biocomposite nanospheres were synthesized in a multiple emulsion. The multiple emulsion was a w/o/w emulsion, made of diammonium phosphate solution as an inner aqueous phase, cyclohexane as an oil phase, and calcium nitrate solution and chitosan solution as an outer aqueous. The forming mechanism of core-shell spheres and the influence of temperature on the morphology of the nanospheres were investigated. The diameter of the resulting core-shell nanospheres was 100-200 nm and the thickness of the chitosan shell was about 10 nm. And it concluded that at different reaction temperature the morphologies of the products would be changed. The core-shell nanospheres have potential applications for the development of new biomedical materials.

Mechanical properties of TiO_2-hydroxyapatite nanostructured coatings on Ti-6Al-4V substrates by APS method

TiO2-hydroxyapatite （HA） nanostructured coatings were produced by atmospheric plasma spray method. The effects of starting powder composition and grain size on their mechanical properties were investigated. The microstructure and morphology were characterized by X-ray diffraction and scanning electron microscopy （SEM）. It is found that the coating with 10% HA has the best mechanical properties. Based on Rietveld refinement method, the mean grain size of the as-received powder （212 nm） extensively decreases to 66.4 nm after 20 h of high-energy ball milling. In spite of grain growth, the deposited coatings maintain their nanostructures with the mean grain size of 112 nm. SEM images show that there is a lower porosity in the coating with a higher HA content. Optical microscopy images show that uniform thickness is obtained for all the coatings.

In-vitro degradation behavior of Mg alloy coated by fluorine doped hydroxyapatite and calcium deficient hydroxyapatite

Fluorine-doped hydroxyapatite(FHA) and calcium deficient hydroxyapatite(CDHA) were coated on the surface biodegradable magnesium alloy using electrochemical deposition(ED) technique. Coating characterization was investigated X-ray diffraction(XRD), Fourier-transformed infrared spectroscopy(FTIR), transmission electron microscopy(TEM), scanni electron microscopy(SEM) and energy dispersive X-ray spectroscopy(EDS). The result shows that nano-FHA coated samp presents nano needle-like structure, which is oriented perpendicular to the surface of the substrate with denser and more unifo layers compared to the nano-CDHA coated sample. The nano-FHA coating shows smaller crystallite size(65 nm) compared to t nano-CDHA coating(95 nm); however, CDHA presents thicker layer(19 μm in thickness) compared to the nano-FHA(15 μm thickness). The corrosion behaviour determined by polarization, immersion and hydrogen evolution tests indicates that the nano-FH and nano-CDHA coatings significantly decrease corrosion rate and induce passivation. The nano-FHA and nano-CDHA coatings c accelerate the formation of bone-like apatite layer and significantly decrease the dissolution rate as compared to the uncoated M alloy. The nano-FHA coating provides effective protection to Mg alloy and presents the highest corrosion resistance. Therefore, t nano-FHA coating on Mg alloy is suggested as a great candidate for orthopaedic applications.

Mechanical properties of hydroxyapatite-zirconia coatings prepared by magnetron sputtering

Hydroxyapatite （HA）-zirconium （ZrO2） composite coating was produced by magnetic sputtering on Ti6Al4V titanium alloy substrate, the coatings of 50HA-50ZrO2 and 75HA-25ZrO2 （mass fraction, %） were characterized by scanning electron microscopy, energy disperse spectroscopy, X-ray diffraction and scratch test, respectively, and the effects of HA contents in the coating on residual stress were analyzed. The experimental results show that the phases of HA-ZrO2 composite coatings are HA, ZrO2 and Y2O3, and the HA has a certain decomposition in the combination process, producing TCP and CaO impurity phases. The porous surface of coating is conducive to the growth of bone tissue, and the surface roughness values of 50HA-50ZrO2 and 75HA-25ZrO2 are 1.61 μm and 2.92 μm, respectively. The coating interface is of mechanical integration, the bonding strength values of 50HA-50ZrO2 and 75HA-25ZrO2 are 30 N and 17.5 N, respectively, showing a downward trend with the HA contents increasing. The residual stress values in the coating of 50HA-50ZrO2 and 75HA-25ZrO2 are （-399.1±3.0） MPa, （-343.2±20.3） MPa, respectively, as a result, the appropriate increase of HA contents in the coating will reduce its residual stress.

Preparation and Characterization of Nanosized Hydroxyapatite Particles in AOT Inverse Microemulsion

Nanosized particles of hydroxyapatite (HAP) were synthesized by reacting Ca(H_2PO_4)_2·H_2O solution complex with equimolar Ca(OH)_2 saturated solution in sodium bis(2-ethylhexyl) sulfosuccinate (AOT)/isooctane water-in-oil microemulsion.The formation of microemulsion strongly depended on water content w (w=[H_2O]/[AOT] molar ratio) and concentration of surfactant and cosurfactant (1-octanol).By the variety of conductivity with w and the partial ternary phase diagram derived from a series of demarcation points,we set the basic component of microemulsions:[AOT]=0.1M(mol/dm^3),[1-octanol]=0.1M and w=3-9.Dynamic light scattering (DLS),UV-visible absorbance,TEM analysis and X-ray diffraction were used to characterize the microemulsion,formation of particles and resulting HAP particles.At low water content(w<9),the water pool radius of the droplet in the Ca(H_2PO_4)_2·H_2O microemulsion lineally depended on w.The size of final HAP particles was strongly affected by water content w and reactant concentration.With increasing water content w from 3 to 9,the size of HAP particles increased from 10-20nm to 40-50 nm at reactant concentration [Ca(H_2PO_4)2·H_2O]=12×10^(-3) mol/dm^3.The resulting HAP particles were poorly crystallized and spherical in morphology.

Preparation and Characterization Analysis of Hydroxyapatite/ Gelatin Composite

The hydroxyapatite （ HAp ）/gelatin composite was prepared by self-assembly method. X-ray diffraction confirmed that the inorganic phase in the composite was HAp. The Fourier transform infra-red spectrum （FT-IR） indicated the presence of amide and hydroxyl groups in the composite. The organic-inorganic ratio of the composite is similar to that of the human bone, which was determined by differential thermal analysis （ DTA ） and thermogravimetric analysis （ TGA ）. Transmission Electron Microscopy （TEM） showed that the composite is composed by spindly grains and the rmdtilayer nanostructure can also be seen. Gelatin in the composite assembled orderly and orderly and directionally ; and the HAp crystals grew along the gelatin molecule at nearly the same direction. A model was established to explain the process of the interaction between gelatin and HAp.

Creep-Recovery and Relaxation Behavior of High Density Polyethylene/Hydroxyapatite Nano Particles for Bone Substitutes: Effects of Gamma Radiation

The following article has been retracted due to the fact that it cannot be accepted by the author as a journal publication. The Editorial Board takes a very strong respect to the author’s situation on this matter. This paper published in Journal of Biosciences and Medicines Vol.2 No.2, April 2014, has been removed from this site.

Preparation and Characterization of Hydroxyapatite/γ-Fe_2O_3 Hybrid Nanostructure

The hybrid particles composed of hydroxyapatite （HAp） and ferrite （ γ-Fe203） were synthesized by two-step precipitation method. The effect of reaction temperature on the morphology of the hybrids was also studied. The resultant hybrids were characterized by transmission electron microscopy （TEM） and X-ray diffraction analysis（XRD）. It was found that γ-Fe203 nanoparticles dispersed within the HAp matrix and these hybrids had a feather-like or spherical morphology when synthesized at 90 ℃ or room temperature, respectively. The magnetic properties of the hybrid showed good superparamagnetic feature, and they could be controlled by the external magnetic field.

Diffusion Kinetics of Carbonate Hydroxyapatite (CHAP) for Adsorbing F^- Dissolved in Water

A systematic research was performed about diffusion kinetics of adsorbing F^- dissolved in water for carbonate hydroxyapatite （CHAP） from the natural hydroxyapatite which was modified by adulterating with CO3^2-. The result shows that the speed of F^- adsorption is controlled by membrane diffusion when F^- concentration is relatively low, which is expressed by the kinetic equation of diffusion Q=0.0005（Ci-C）（t-ti）＋0.3967, or by vacancy diffusion when F^- concentration is relatively high, which is expressed by the kinetic equation of diffusion In[C（o, t）]=8.4718-0.5048Int. Based on the feature of CHAP for adsorbing F^- dissolved in water and its special channel of the structure of CO3^3- modified hydroxyapatite, models of vacancy diffusion and membrane diffusion were established.

Studies on Processing and Characterization of Hydroxyapatite Biomaterials from Different Bio Wastes

Development of suitable materials that acts as an interface between the implant and tissues in body system structurally, mechanically and bio functionally is important for the success of tissue engineering. This motivated materials scientists and biologists to find out suitable bioactive materials for the aforementioned purpose. There has been growing interest in developing bioactive synthetic ceramics that could closely mimic natural apatite characteristics. Hydroxyapatite (HAp) has been widely used as a biocompatible ceramic but mainly for contact with bone tissue, due to its resemblance to mineral bone. This study presents the synthesis and characterization of HAp materials from different sources like bovine bone and fish scales and their application in tissue engineering. The phase purity and crystallinity of different calcined HAp powder was determined by XRD and FTIR analysis. The Thermo Gravimetric and Differential Thermal Analysis were carried out to show the thermal stability of the HAp powder. The morphology of the powder was observed under Scanning Electron Microscopy (SEM). Cytotoxicity evaluation of the developed powder was carried out in RAW macrophage like cell line media for an incubation period of 72 hours. These results proved the biocompatibility of HAp powders obtained from different biosources for tissue engineering applications.

Drug Release Characteristics of Hydroxyapatite Bone Cement

To discuss the feasibility of bydroxyapatite bone cement （HAC） used as a drug delivery carrier and observe the bacteriostatic activity of HAC/ Norvancomycin（ HAC/ NVCM ） composite in vitro and its release characteristics in vivo. Bacteriostatic zone and cycle of composite containing 1.5wt% of NVCM were measured in vitro studies. In vivo stndies , the composite was implanted into the top of rabbit＇ s tibia as the local medication group, HAC without NVCM being composed was also implanted and NVCM was injected into auricular vein as the systemic medication group. Cnncentrations of NVCM in blood and local bone were measured in both groups at different time points. The experimental results showed that HAC did not influence the bacteriostatic activity of NVCM otviously, and NVCM exist in the porosities of HAC in the pattern of amorphism. The blood coueemrations of NVCM in local medication group were always lower than those in systemic medication group at any time point, while the bone concentrations of NVCM in local medication group were much higher than those of systemic medication group,which remained to be 3.96μg/mg/mL after 2 weeks. And HAC has good release characteristics as a drug delivery earricr.