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.

Bio-inspired Hydroxyapatite/Gelatin Transparent Nanocomposites

Hydroxyapatite(HA)nanoparticles impart outstanding mechanical properties to organicinorganic nanocomposites in bone.Inspired by the composite structure of HA nanoparticles and collagen in bone,a high performance HA/gelatin nanocomposite was first developed.The nanocomposites have much better mechanical properties(elongation at break 29.9%,tensile strength 90.7 MPa,Young’s modulus 5.24 GPa)than pure gelatin films(elongation at break 9.3%,tensile strength 90.8 MPa,Young’s modulus 2.5 GPa).In addition,the composite films keep a high transmittance in visible wavelength range from 0%to 60%of the HA solid content.These differences in properties are attributed to the homogeneous distribution of HA nanoparticles in the gelatin polymer matrix and the strong interaction between the particle surfaces and the gelatin molecules.This protocol should be promising for HA-based nanocomposites with enhanced mechanical properties for biomedical applications.

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.

Ionic liquid-assisted preparation of hydroxyapatite and its catalytic performance for decarboxylation of itaconic acid

The synthesis of methacrylic acid from biomass-derived itaconic acid is a green route,for it can get rid of the dependence on fossil resource.In order to solve the problems on this route such as use of a preciousmetal catalyst and a corrosive homogeneous alkali,we prepared a series of hydroxyapatite catalysts by an ionic liquid-assisted hydrothermal method and evaluated their catalytic performance.The results showed that the ionic liquid[Bmim]BF_(4) can affect the crystal growth of hydroxyapatite,provide fluoride ion for fluorination of hydroxyapatite,and adjust the surface acidity and basicity,morphology,textural properties,crystallinity,and composition of hydroxyapatite.The[Bmim]BF4 dosage and hydrothermal temperature can affect the fluoride ion concentration in the hydrothermal system,thus changing the degree of fluoridation of hydroxyapatite.High fluoride-ion concentration can lead to the formation of CaF_(2) and thus significantly decrease the catalytic performance of hydroxyapatite.The hydrothermal time mainly affects the growth of hydroxyapatite crystals on the c axis,leading to different catalytic performance.The suitable conditions for the preparation of this fluoridized hydroxyapatite are as follows:a mass ratio of[Bmim]BF4 to calcium salt=0.2:1,a hydrothermal time of 12 h,and a hydrothermal temperature of 130℃.A maximal methacrylic acid yield of 54.7%was obtained using the fluoridized hydroxyapatite under relatively mild reaction conditions(250℃ and 2 MPa of N_(2))in the absence of a precious-metal catalyst and a corrosive homogeneous alkali.

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.

Preparation of Fish Scales Hydroxyapatite (FsHAp) for Potential Use as Fillers in Polymer

The aims of this study were to prepare natural hydroxyapatite from fish scales(FsHAp)for potential use as a filler in polymer.The FsHAp was prepared from Tilapia fish scales using thermal method.The FsHAp was milled for 48 h and dried by spray method.The morphology was characterized using field emission scanning electron microscope(FESEM)which showed irregular shape of FsHAp particles with particle size around 7μm.The analysis of FsHAp was carried out using Fourier transform infrared spectroscopy(FTIR)and X-ray diffraction(XRD)to confirm chemical structure of FsHAp.

Influence of anodization conditions on deposition of hydroxyapatite onα/βTi alloys for osseointegration:Atomic force microscopy analysis

Integrating titanium-based implants with the surrounding bone tissue remains challenging.This study aims to explore the impact of different anodization voltages(20−80 V)on the surface topography of two-phase(α/β)Ti alloys and to produce TiO_(2) films with enhanced bone formation abilities.Scanning electron microscopy coupled with energy dispersive spectroscopy(SEM−EDS)and atomic force microscopy(AFM)were applied to investigate the morphological,chemical,and surface topography of the prepared alloys and to confirm the growth of hydroxyapatite(HA)on their surfaces.Results disclosed that the surface roughness of TiO_(2) films formed on Ti−6Al−7Nb alloys was superior to that of Ti−6Al−4V alloys.Ti−6Al−7Nb alloy anodized at 80 V had the highest yields of HA after immersion in simulated body fluid with enhanced HA surface coverage.The developed HA layer had a mean thickness of(128.38±18.13)μm,suggesting its potential use as an orthopedic implantable material due to its promising bone integration and,hence,remarkable stability inside the human body.

Studies of XRD and FTIR on Synthesized Novel Hybrid Thin Film Made of Hydroxyapatite, Poly Vinyl Alcohol and Gelatin for Biomedical Application

With the modern advancement of treatment approaches in medical science, the application of biomaterials in tissue engineering provides a remarkable opportunity to overcome graft rejection as well as proper wound healing. In this study, novel hybrid films have been synthesized by incorporation of polyvinyl alcohol (PVA), gelatin, and gelatin with glycerin along with different concentrations of pre-prepared hydroxyapatite (HAP) by solution casting method at room temperature in a biosafety cabinet. Glutaraldehyde has been added as a crosslinker in this whole procedure. Fourier-transform infrared spectroscopy (FTIR), X-Ray Diffraction (XRD) have been conducted to observe and compare the structural and chemical stability of the synthesized hybrid film properties. The FTIR results and X-Ray Diffraction analyses confirmed the chemical interactions between HAP, PVA, gelatin, and glycerin have occurred. The crystallinity of HAP also remains in all the prepared hybrid film samples that are observed in XRD. It is expected that these newly synthesized hybrid films could be a better opportunity for various sectors of tissue engineering such as skin, bone, tendon, and cartilage. These synthesized hybrid films can be suitable for wound healing covering. These studies could be a new scope for long-term drug delivery directly on wound sites in diabetic gangrene foot or burn patients as well as cartilage or joint replacement therapy.

Development and Characterization of Hybrid Film Made of Hydroxyapatite, Poly Vinyl Alcohol and Gelatin for Biomedical Application

In the recent research field of bone tissue engineering, polymeric materials play an implacable role in mimes the natural behavior of hard and soft tissues. In some medical conditions such as diabetics, osteoarthritis, burns, or joint replacement conditions, this polymeric materials implication enhances the internal mechanical activities which result in the early recovery of disease by facilitating the wound healing process. In this study, hybrid films have been synthesized based on polyvinyl alcohol (PVA), gelatin, and gelatin with glycerin incorporated with different concentrations of pre-prepared hydroxyapatite (HAP) by solution casting method at room temperature in biosafety cabinet. Glutaraldehyde has been added as a crosslinker in this whole procedure. The mechanical property, swelling, and porosity percentage have been conducted to characterize the structural stability of the synthesized hybrid films. Porosity and swelling of samples are also represented by proper biocompatibility (>90% porosity and swelling in DDW and PBF vary between 287%~72%). Tensile strength (TS), E modulus (Young’s modulus), Elongation at maximum, and Elongation at break are observed to perceive the mechanical properties of hybrid film samples, which are compatible with mechanical properties of different tissue such as trabecular bone, articular cartilage, tendon, nerve and skin tissue. Though, biocompatibility tests both in vivo and in vitro are essential for clinical application in the future. However, the experiment carried out till now explains the true possibility of newly synthesized hybrid films for long-term drug delivery directly on wound sites for wound healing and burn dressing patients in head-neck surgery reconstruction, diabetic gangrene foot, as well as cartilage or joint replacement therapy.

Hydroxyapatite/Alginate Nanocomposite: In Situ Processing and Properties for Biomedical Applications

The development of advanced biomaterials is crucial for addressing the increasing demand for improved medical implants and tissue engineering scaffolds. Hydroxyapatite (HAp), a naturally occurring mineral form of calcium apatite, is widely recognized for its excellent biocompatibility and osteoconductivity, making it an ideal candidate for bone-related applications. However, its brittleness and lack of flexibility limit its broader application in dynamic biological environments. To overcome these limitations, this study explores the synthesis of Hydroxyapatite/Alginate (HAp/Alg) nanocomposites, leveraging the biocompatibility and flexibility of alginate—a natural polysaccharide derived from brown seaweed. The HAp/Alg nanocomposites were synthesized using in situ hybridization techniques with varying alginate concentrations (10 to 40 wt%) to optimize their structural and functional properties. The motivation behind this work lies in the potential of these composites to combine the desirable properties of both HAp and alginate, resulting in a material that not only mimics the mineral composition of bone but also offers enhanced flexibility and structural integrity. A comprehensive analysis was conducted using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis/Differential Thermal Analysis (TGA/DTA), Scanning Electron Microscopy (SEM), and cytotoxicity testing to evaluate the structural, chemical, and biological properties of the composites. XRD analysis indicated a complex interaction between alginate concentration and crystal growth, with crystallite size increasing up to 10 wt% alginate before decreasing. FT-IR spectra confirmed significant biological reactivity at the composite’s surface and within the polymer matrix, suggesting strong potential for biological interactions. SEM images revealed a more uniform microstructure in HAp/Alg composites compared to pure HAp, which is likely to improve their performance in biomedical applications. TGA/DTA results demonstrated the thermal stability of the composites across various temperature conditions, while cytotoxicity tests confirmed their biocompatibility, making them suitable for use in medical applications. This study not only successfully synthesizes HAp/Alg nanocomposites with enhanced structural uniformity and biocompatibility but also provides a promising avenue for the development of next-generation biomaterials that could significantly impact the field of regenerative medicine and biomedical engineering.

Flexoelectricity in hydroxyapatite for the enhanced piezocatalytic degradation of phenanthrene in soil

Coupling the effects of flexoelectricity with piezoelectricity has been proved to effectively harvest mechanical energy.In this study,a composition-graded core–shell structure(HAP@FAP)was prepared by surface-gradient F-doping in hydroxyapatite,which could introduce flexoelectricity by a built-in strain gradient.A flexoelectric-boosted piezoelectric response was demonstrated by piezoresponse force microscopy(PFM)characterization,showing that the piezoelectric constant of HAP@FAP was increased by 2.25 times via a lattice strain gradient induced by chemical heterogeneities derived from the unique composition-graded core-shell structure.Thus,the piezocatalytic activity of HAP@FAP for phenanthrene(PHE)degradation in soil was enhanced.This work provides a new strategy for the modification of piezoelectric catalysts for the remediation of organics-contaminated soils on industrial land.

Effect of cetyltrimethylammonium bromide on morphology and porous structure of mesoporous hydroxyapatite

The mesoporous hydroxyapatite （HA） was synthesized by hydrothermal method utilizing cationic surfactant cetyltrimethylammonium bromide （CTAB） as template. The crystalline phase, morphology and porous structure were characterized respectively by different detecting techniques. The results reveal that the particles are highly crystalline hydroxyapatite phase. The surfactant has little influence on the morphology of the crystals, but affects the porous structure obviously. The sample without CTAB has a low surface area not exceeding 33 m^2/g, and no distinct pores can be observed by TEM. While the samples obtained with the surfactant get better parameters. Numerous open-ended pores centered at 2-7 nm spread unequally on the surface of the hydroxyapatite nanorods. The N2 adsorption-desorption experiments show type IV isotherms with distinct hysteresis loops, illustrating the presence of mesoporous structure. When the mole ratio of CTAB to HA is 1：2, the sample has the largest surface area of 97.1 m^2/g and pore volume of 0.466 cm^3/g.

Arginine functionalized hydroxyapatite nanoparticles and its bioactivity for gene delivery

In order to further improve the transfection efficiency of hydroxyapatite nanoparticle （HAp）, arginine functionalized hydroxyapatite （HAp/Arg） was synthesized by hydrothermal synthesis. The morphology, crystallite size and zeta potential of the HAp/Arg were characterized by transmission electron microscopy （TEM）, atomic force microscopy （AFM） and zeta potential analyzer. The loading and protecting properties of HAp/Arg to DNA were tested by electrophoresis. Its cytotoxicity was also measured in Hela cells and HAEC cells by MTT and LDH, and its transfection efficiency was examined by fluorescence microscope and flow cytometry. The results reveal that HAp/Arg is short rod-like and nano single crystal, the mean diameter is 50-90 nm and zeta potential is 35.8 mV at pH 7.4. HAp/Arg to DNA can be condensed by electrostatic effect and protect DNA against degradation in DNase I, and shows high transfection efficiency without cytotoxicity. These results suggest that HAp/Arg can be a promising alternative as a novel gene delivery system.

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.

Effects of Nanometer Hydroxyapatite on Proliferation of Periodontal Ligament Fibroblasts

Objective:To investigate possible effects of nanophase powder of hydroxyapatite on proliferation of periodontal ligament cells. Methods: With sol-gel method, the nanophase hydroxyapatite powders were fabricated. These powders were proved nanopaticles by transmission electron microscope. The effects on proliferation of periodontal ligament cell(PDLC) were observed in vitro with MTT [3-(4,5dimethylthiazo;-2-yl)-2,5-diphenytetralium bromide] method. Results: On the 2nd,3rd,4th day after treated with nanoparticles of hydroxyapatite, the proliferate activity of the PDLC increases significantly, compared with those with dense hydroxyaoatite and control but no significant difference could be found between the dense hydroxyapatite and the control. Conclusion: Nanophase hydroxyapatite can promote the regeneration of periodontal tissue.

Polymeric nanocomposites loaded with fluoridated hydroxyapatite Ln^(3+)(Ln = Eu or Tb)/iron oxide for magnetic targeted cellular imaging

Objective： To fabricate polymeric nanocomposites with excellent photoluminescence, magnetic properties, and stability in aqueous solutions, in order to improve specificity and sensitivity of cellular imaging under a magnetic field. Methods： Fluoridated LnS＋-doped HAP （Ln3＋-HAP） NPs and iron oxides （lOs） can be encapsulated with biocompatible polymers via a modified solvent exaction/evaporation technique to prepare polymeric nanocomposites with fluoridated Ln3＋-HAP/iron oxide. The nanocomposites were characterized for surface morphology, fluorescence spectra, magnetic properties and in vitro cytotoxicity. Magnetic targeted cellular imaging of such nanocomposites was also evaluated with confocal laser scanning microscope using A549 cells with or without magnetic field. Results： The fabricated nanocomposites showed good stability and excellent luminescent properties, as well as low in vitro cytotoxicity, indicating that the nanocomposites are suitable for biological applications. Nanocomposites under magnetic field achieved much higher cellular uptake via an energy-dependent pathway than those without magnetic field. Conclusion： 1tie nanocomposites fabricated in this study will be a promising tool for magnetic targeted cellular imaging with improved specificity and enhanced selection.

rGO/CdS@HAP复合微球的光催化活性增强机理

为提升CdS基复合材料的光催化活性和稳定性,运用水热法在CdS@HAP(羟基磷灰石)微球表面包覆rGO(还原氧化石墨烯)并制备rGO/CdS@HAP光催化材料,利用XRD(X射线衍射)、SEM(扫描电子显微镜)、UV-vis(紫外-可见吸收光谱)等手段分析材料的晶体结构和理化性质,结合MB(亚甲基蓝)的光催化降解实验探讨rGO/CdS@HAP的光催化活性增强机理。结果表明:rGO/CdS@HAP具有中空微球结构,直径4—5μm,rGO以薄纱状均匀包裹在CdS@HAP表面;rGO/CdS@HAP具有优异的可见光吸收能力,在可见光辐射120 min后对MB的去除率高达94%,在光催化循环实验中表现出优异的光催化活性和稳定性。机理分析证实,由CdS和HAP构建的Ⅰ型异质结带隙较窄,有助于提升复合材料对可见光的吸收和利用,rGO在CdS@HAP表面的包覆提升载流子分离效率的同时为光生空穴提供高速的传输路径,有效抑制CdS的光腐蚀,从而实现rGO/CdS@HAP光催化活性和稳定性的显著增强。

ZnS@CdS/HAP复合微球的SILAR法制备及光催化性能

以酵母模板法制备的中空羟基磷灰石(HAP)微球为基底,通过连续离子层吸附反应法(SILAR)制备ZnS@CdS/HAP复合微球,利用XRD、SEM、UV-vis等表征手段分析材料的晶体结构、微观形貌和光吸收能力等,同时结合亚甲基蓝的光催化降解实验探讨复合微球的光催化机理.结果表明:利用SILAR法成功实现了ZnS@CdS/HAP复合微球的制备,ZnS@CdS/HAP复合微球的直径约为3~5μm且分散性良好,在可见光区有良好的吸收性能,具有优异的光催化活性,在催化剂添加量1g/L、pH=7、温度为25℃的条件下,对50mL浓度为10mg/L的亚甲基蓝溶液可见光催化100min时去除率高达93%.机理分析证实,ZnS@CdS/HAP光催化可能存在的Z型电荷迁移机制在有效抑制光生载流子复合的同时有效抑制光生腐蚀的发生,提升了ZnS@CdS/HAP复合微球的光催化活性和稳定性.

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.