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.

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.

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.

Influence of Ca/P ratio on the catalytic performance of hydroxyapatite for decarboxylation of itaconic acid to methacrylic acid

Methacrylic acid,an important organic chemical,is commercially manufactured starting from fossil feedstock.The decarboxylation of itaconic acid derived for biomass is a green route to the synthesis of methacrylic acid.In view of the problems existing in the researches on this route such as use of noble metal catalyst,harsh reaction conditions and low desired-product yield,we prepared a series of hydroxyapatite catalysts with different Ca/P molar ratios and evaluated their catalytic performance.The results showed that the hydroxyapatite catalyst with a Ca/P molar ratio of 1.58 had the best catalytic activity.The highest yield of MAA up to 61.2%was achieved with basically complete conversion of itaconic acid under the suitable reaction conditions of 1 equivalent of NaOH,2 MPa of N_(2),250℃,and 2 h.On this basis,a reaction network for the decarboxylation of itaconic acid to methacrylic acid catalyzed by hydroxyapatite was established.With the aid of catalyst characterization using X-ray powder diffraction,NH3/CO2 temperature-programmed desorption,N_(2)physisorption,inductively coupled plasma optical emission spectrometry,and scanning electron microscopy,we found that the distribution of surface acid sites and basic sites,crystal growth orientation,texture properties and morphology of hydroxyapatite varied with the Ca/P molar ratio.Furthermore,the change of the crystal growth orientation and its influence on the surface acidity and alkalinity were clarified.

Hydroxyapatite-containing PEO-coating design for biodegradable Mg-0.8Ca alloy: Formation and corrosion behaviour

In this study, the biocompatible protective coating was formed using plasma electrolytic oxidation(PEO) on bioresorbable Mg-0.8Ca alloy. The composition of the formed coating was studied using XRD, SEM-EDX analysis, and micro-Raman spectroscopy. The uniform distribution of hydroxyapatite over the thickness of protective PEO-layer was established. Using traditional(EIS, PDP, OCP) and local scanning electrochemical methods(SVET, SIET with H^(+)-selective microelectrode), the level of protective properties of PEO-layer in a biological environment(mammalian cell culture medium, MEM) was determined. It was established that modification of Mg-0.8Ca alloy surface by PEO contributes to a significant increase in the corrosion resistance of the surface layer, making it possible to control the process of material‘s biodegradation. The maximum local electrochemical activity was recorded after 72 h of testing, while for the uncoated sample,intense corrosion degradation was recorded in the first 12 min of exposure to the cell culture medium. Formation of the PEO-coating results in a twofold decrease in the corrosion current density(2.8·10^(-6)A cm^(-2)) and an increase in the impedance modulus measured at a low frequency(1.7·10^(4)Ω cm^(2)) in comparison with the uncoated material(9.5·10^(-6)A cm^(-2);8.1·10^(3)Ω cm^(2)). The mechanism of material bioresorption was established and a model for biodegradation process of Mg-0.8Ca alloy with hydroxyapatite-containing PEO-coating in MEM was proposed. Analysis of these results and comparing with others obtained by various scientific groups indicate the prospects for application of biocompatible PEO-coating on Mg-Ca alloy in implant surgery.

Corrosion behavior of composite coatings containing hydroxyapatite particles on Mg alloys by plasma electrolytic oxidation: A review

Mg and its alloys have been introduced as promising biodegradable materials for biomedical implant applications due to their excellent biocompatibility, mechanical behavior, and biodegradability. However, their susceptibility to rapid corrosion within the body poses a significant challenge and restricts their applications. To overcome this issue, various surface modification techniques have been developed to enhance the corrosion resistance and bioactivity of Mg-based implants. PEO is a potent technique for producing an oxide film on a surface that significantly minimizes the tendency to corrode. However, the inevitable defects due to discharges and poor biological activity during the coating process remain a concern. Therefore, adding suitable particles during the coating process is a suitable solution. Hydroxyapatite(HAp)has attracted much attention in the development of biomedical applications in the scientific community. HAp shows excellent biocompatibility due to its similarity in chemical composition to the mineral portion of bone. Therefore, its combination with Mg-based implants through PEO has shown significant improvements in their corrosion resistance and bioactivity. This review paper provides a comprehensive overview of the recent advances in the preparation, characterization, corrosion behavior and bioactivity applications of HAp particles on Mg-based implants by PEO.

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.

2022-2023年山东省A(H1N1)pdm09流感病毒HA、NA基因变异特征分析

目的 了解山东省2022-2023流感监测年度分离的A(H1N1)pdm09亚型流感病毒血凝素(hemagglutinin,HA)和神经氨酸酶(neuraminidase,NA)基因的变异特征,为流感的防控提供科学依据。方法 从流感监测网络实验室分离的流感毒株中按地市随机选取14株A(H1N1)pdm09亚型流感毒株,以WHO推荐的当季疫苗株为参考进行全基因组测序,并采用荧光法开展神经氨酸酶抑制(neuraminidase inhibition,NI)实验以评估药物敏感性。结果 山东省2022-2023年度分离的A(H1N1)pdm09流感病毒属于6B.1A分支中的5a.2a进化簇,核苷酸序列比对分析显示,HA和NA基因与2021-2023年度北半球疫苗株A/Victoria/2570/2019的亲缘关系较为接近,同源性分别为98.5%~98.7%和98.8%~99.1%。氨基酸序列分析显示,HA蛋白有20个位点发生了氨基酸序列变异,并发现1株病毒可能发生抗原漂移,有3株病毒发生了HA蛋白糖基化位点的缺失。NA酶相关重要位点未发生变异。NI实验显示,所测流感毒株均对抗流感病毒药物敏感。结论 所监测毒株与疫苗株整体同源性很高,但氨基酸存在一定程度变异,今后有必要持续开展流感病毒基因变异特征监测以了解流感流行的风险,以及评价基因变异对流感疫苗和治疗药物效果的影响。

电化学沉积时间对碱预处理钛合金表面HA涂层的影响

采用碱预处理钛合金表面再电化学沉积的方法,研究了电化学沉积时间对羟基磷灰石(HA)涂层物相、形貌、生物活性及其与钛合金基体间结合强度的影响。结果表明,碱预处理钛合金表面制备的电化学沉积涂层主要由片状HA相组成,电化学沉积时间对涂层物相组成没有影响,但会影响涂层厚度;沉积时间60 min时得到的HA涂层较致密,与基体的结合强度达17.85 MPa。各沉积时间下得到的HA涂层均具有较好的生物活性,在模拟体液(SBF)中,CO_(3)^(2-)置换HA中的PO_(4)^(3-)进入磷灰石中形成类骨磷灰石CHA,呈馒头状,直径7~8μm,且在SBF中浸泡3 d,CHA可铺满HA表面。

HA380血液灌流与血液滤过治疗脓毒症相关凝血功能障碍的疗效研究

脓毒症是ICU患者常见的一种严重的器官功能障碍,是由多种感染因素引起的人体免疫功能失调,导致过度的全身炎症反应,进而诱发凝血功能障碍,即脓毒症相关凝血功能障碍(SAC),其特点是凝血反应增强、抗凝-纤溶途径受损[1],并可引起多器官功能障碍,凝血激活的程度和调节,影响患者预后[2]。严重者可进展为弥散性血管内凝血,导致死亡。有研究表明,早期连续血液净化治疗可以改善脓毒症患者凝血功能指标[3];HA380血液灌流可以降低人体内的炎症反应,改善微循环障碍,降低器官功能损害[4]。为此,本研究对二者的临床效果进行了观察比较。

基于SPARTA框架的HAS4决赛攻击路径分析

太空网络面临的安全威胁越来越多,美国自2020年起,连续四年举办黑掉卫星(Hack-A-Sat,HAS)挑战赛,并发射真实卫星“月光者”用于HAS比赛。太空攻击研究与战术分析框架SPARTA是针对太空网络安全的对抗战术和技术知识库。借助SPARTA框架,详细分析了第四届HAS决赛中攻击使用的战术技术,对于深入理解SPARTA框架、太空网络安全具有一定借鉴意义。

血液灌流(HA380)联合血液净化(CVVH)治疗在脓毒症患者中的临床研究

探讨血液灌流(HA380)联合血液净化(CVVH)在脓毒症治疗中的临床优势与效果。方法 自入住滨州市人民院患者中按照纳入标准和排除标准选择脓毒症患者40例,分为对照组20和观察组20例,观察组患者在常规治疗基础上行血液灌流(HA380)+CVVH方案治疗,对照组患者行常规脓毒症诊疗+CVVH方案治疗,比较两组患者在治疗前后的炎症指标水平以及病情危重程度(SOFA评分和APECHEII评分)各指标的改善情况以及28天死亡率等,并进行统计学分析。结果 治疗前,两组炎症指标(PCT、TNF-α和IL-6)和预后(APACHEⅡ和SOFA)等相关指标对比差异无统计学意义(P>0.05);治疗后,两组炎症指标(PCT、IL-6和TNF-α)、预后的指标(SOFA和APACHEⅡ)均有所降低,且观察组变化幅度大于对照组(P<0.05)。28天死亡率无差别。结论 HA380串联CVVH治疗模式比单纯CVVH治疗模式在治疗脓毒症方面更能降低患者体内的炎症介质水平,改善血流动力学和增加组织器官灌注,减轻全身感染症状,最终改善患者病情严重程度。

表达H7N9亚型禽流感病毒HA蛋白的重组血清4型禽腺病毒构建及其免疫效果评估

为构建H7N9亚型禽流感病毒和血清4型禽腺病毒(FAdV-4)的二联疫苗候选株,试验通过CRISPR/Cas9和Cre-Loxp系统,以课题组前期构建的表达EGFP蛋白的重组病毒FAdV4-EGFP为载体,构建能够稳定表达H7N9亚型禽流感病毒血凝素(HA)蛋白的重组血清4型腺病毒;并通过PCR、间接免疫荧光试验(IFA)、Westernblot试验以及SPF鸡保护性试验等方法,探究此重组病毒体外生物学特性并评估其为鸡提供的保护力。结果显示:研究成功构建能稳定表达H7N9禽流感亚型病毒HA蛋白的重组血清4型腺病毒,命名为FAdV4-H7;FAdV4-H7能在LMH细胞高效复制,并能在LMH细胞传代15次后仍能稳定表达HA蛋白;FAdV4-H7不仅高度致弱,而且能诱导机体产生高滴度针对H7N9亚型禽流感病毒HI抗体和FAdV-4的中和抗体,能为SPF鸡提供足够保护来抵抗致死性FAdV-4感染。研究表明,试验成功构建了重组病毒FAdV4-H7,为H7N9亚型禽流感病毒和FAdV-4的联防联控提供了二联苗候选疫苗株。

基于Galileo HAS服务的全球PWV反演验证分析

基于实时精密单点定位PPP的大气可降水量PWV反演技术近年来受到广泛研究,但目前该技术大多需利用网络通讯接收改正信息,这使其在通讯网络不能覆盖及因灾通讯受限地区的使用受到限制。2023年1月开通服务的Galileo系统高精度定位服务HAS(High Accuracy Service)为实现不依赖额外通讯手段的实时PWV反演提供了新手段。本文首先分析验证了Galileo系统HAS服务的卫星轨道和钟差改正信息精度,并将基于武汉大学IGS分析中心产品的PWV反演结果作为内部对比参考值、将基于ERA5数据及探空数据结果作为PWV结果对比的外部参考值,验证了基于HAS服务的PWV反演精度。结果表明HAS服务反演得到的PWV与两类参考值均具有较高的一致性。其中HAS服务计算得出的结果与IGS事后产品PWV解算结果的两序列差的RMS为2.91 mm,与探空数据的序列差的RMS为2.51 mm。初步验证了HAS可用于降雨的短时预报可行性。

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.

H5N1亚型禽流感病毒HA蛋白在水稻胚乳中的表达及其纯化

为制备H5N1亚型禽流感病毒HA蛋白并评估其免疫原性,利用水稻表达系统表达H5N1亚型禽流感病毒重组HA蛋白。首先构建了重组植物表达载体pCAMBIA1300-HA,该载体具有GT13特有启动子、信号肽SP和终止子,有利于外源基因在水稻中表达。之后将重组质粒pCAMBIA1300-HA通过电转化法导入根癌农杆菌EHA105中,筛选出阳性菌落并侵染水稻愈伤组织。经过暗培养、潮霉素筛选、分化、生根、成苗,采用CTAB法提取水稻叶片DNA,PCR鉴定结果显示,HA基因已插入到水稻基因组中,重组HA基因大小为4660 bp。将阳性植株移植到大田中,4个月后收获水稻种子,提取水稻胚乳蛋白,Western blot鉴定结果表明,HA蛋白在水稻胚乳中成功表达。重组HA蛋白通过Q阴离子层析、疏水层析和凝胶过滤层析三步分离纯化,其纯度达到90%以上。最后将纯化后的重组HA蛋白与ISA 50V佐剂混合并乳化制成疫苗,免疫小鼠,小鼠血清具有较高的特异性抗体水平,表明重组HA蛋白免疫原性较好。综上,成功构建了H5N1亚型禽流感病毒HA重组蛋白的水稻表达系统,并分离纯化获得了高纯度和免疫原性良好的重组HA蛋白。

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.