低免疫原性猪真皮支架制备及其细胞相容性评价

目的观察基质金属蛋白酶7（MMP-7）、京尼平及真空冷冻干燥处理对猪脱细胞网状层真皮基质组织结构及细胞相窬性的影响。方法取清洁级健康大约克夏猪边腹部皮肤，采用机械法制作54块网状层真皮，面秋10．0mm×5．0mm，厚0．5～0．6mm，按随机数字表法分为正常对照绀（A。组，小仃处娌）、脱细胞组（B组，行脱细胞处理）、脱细胞＋MMP-7组（C组，行脱细胞和MMP-7处理）、脱细胞＋MMP-7＋京尼平组（D组，脱细胞处理后用MMP-7和京尼平处理）和脱细胞＋MMP-7＋康皑平＋真窄冷冻干燥组（E组，除行D组处理外，加真空冷冻了：燥处理），A，组6块，其余每组均为12块、，乃取6块卡相同面积人ADM没为人ADM组（A，组，不行处理），即细胞相容性实验中的对照组、采用HE染色、扫描电镜检测A1、B～E组真皮支架中细胞数量及组织结构变化，采用免疫组织化学染色法俭测A1、B、C组样本中波形蛋白、层粘连蛋白（LN）、Ⅳ型胶原蛋白残留情况，采用细胞毒性试验榆测B～E组浸提液的细胞毒性。接种人Fb于B～E组和A，组真皮支架表面培养，观察培养3、7、14d时Fb生长情况，采用ELISA法检测培养3、7d上清液中IL-6、IL-8含量。对数据进行双因素办差分忻及LSD-t检验。结果A1组可见含毛囊的浅黄色颗粒状结构，B组标本毛囊内仍有少艟毛发、上皮根鞘、细胞核、细胞碎片样结构及波形蛋白、LN、1V型胶原蛋白残留，C～E组经MMP-7处理后上述物质被完个去除。大体观察显示，D、E组真皮支架韧性较B、C组增加。C～E组胶原纤维结构亢褴，排列与A．组卞日似儿胶原纤维之间间隙增大，其中C、D组间隙卡H近但均大于B组，E组最大．B～E组真皮支架浸捉液细胞毒性为0或1级。F11于A2和B～E组真皮支架上均能增殖，并且随培养时问延长逐渐由单层变成复层生长进而向标本内部生长。D、E组真皮表面细胞密度较高，A1、C组细胞则主要存在于组织内邦。培养7d，A1、B～E组培养上清液中IL-6含请分别为（132±14）、（104±9）、（122±14）、（120±12）、（128±17）pg／mL，IL-8含量分别为（135±18）、（102±17）、（127±18）、（134±23）、（141±24）pg／mL，分别较培养3d的（55±13）、（34±8）、（48±8）、（50±13）、（49±12）pg／mL和（93±19）、（63±11）、（82±15）、（82±16）、（89±16）pg／mL明显增高（，值分别为98．869、184．038、125．531、93．237、87．265和15．694、23．451、22．801、19．607、18．808，P值均小于0．05）；M-时相点A1、B～E纽纽间IL-6、IL-8含髓比较，差异均有统计学意义（F值分别为2．809、3．301±3．757、3．266，P值均小于0．05）；LSD-t检验结果表明，A1、C～E组组间IL-6、IL-8含避比较差异尤统计学意义（t值分别为0．058～1．905、0．034～1．295，P值均大于0．05），但均较B组高（t值分别为3．707～5．612、2．785～4．079，P值均小于0．05）。结论脱细胞联合MMP．7、京尼平及真宅冷冻干燥方法制备的低免疫原性猪真皮支架具有较好的细胞相容性，细胞长人组织内部较少可能与京尼平增加组织韧性有关。

Design and characterization of biodegradable Mg-Zn-Ag metallic glasses

In order to develop the Mg-Zn-Ag metallic glasses(MGs)for biodegradable implant applications,the glass formation ability(GFA)and biocompatibility of Mg-Zn-Ag alloys were investigated using a combination of the calculation of phase diagrams(CALPHAD)and experimental measurements.High GFA potentiality of two alloy series,specifically Mg_(96-x)Zn_xAg_(4)and Mg_(94-x)Zn_xAg_6(x=17,20,23,26,29,32,35),was predicted theoretically and then substantiated through experimental testing.X-ray diffraction(XRD)and differential scanning calorimetry(DSC)techniques were used to evaluate the crystallinity,GFA,and crystallization characteristics of these alloys.The results showed that compositions between Mg_(73)Zn_(23)Ag_(4)and Mg_(64)Zn_(32)Ag_(4)for Mg_(96-x)Zn_xAg_4,Mg_(66)Zn_(28)Ag_(6)and Mg_(63)Zn_(31)Ag_(6for)Mg_(94-x)Zn_xAg_(6)displayed a superior GFA.Notably,the GFA of the Mg_(96-x)Zn_xAg_(4)series was better than that of the Mg_(94-x)Zn_xAg_(6)series.Furthermore,the Mg_(70)Zn_(26)Ag_4,Mg_(74)Zn_(20)Ag_6,and Mg_(71)Zn_(23)Ag_(6)alloys showed acceptable corrosion rates,good cytocompatibility,and positive effects on cell proliferation.These characteristics make them suitable for applications in medical settings,potentially materials as biodegradable implants.

Laser processing effects on Ti−45Nb alloy surface,corrosive and biocompatible properties

The Ti−45Nb(wt.%)alloy properties were investigated in relation to its potential biomedical use.Laser surface modification was utilized to improve its performance in biological systems.As a result of the laser treatment,(Ti,Nb)O scale was formed and various morphological features appeared on the alloy surface.The electrochemical behavior of Ti−45Nb alloy in simulated body conditions was evaluated and showed that the alloy was highly resistant to corrosion deterioration regardless of additional laser surface modification treatment.Nevertheless,the improved corrosion resistance after laser treatment was evident(the corrosion current density of the alloy before laser irradiation was 2.84×10^(−8)A/cm^(2),while that after laser treatment with 5 mJ was 0.65×10^(−8)A/cm^(2))and ascribed to the rapid formation of a complex and passivating bi-modal surface oxide layer.Alloy cytotoxicity and effects of the Ti−45Nb alloy laser surface modification on the MRC-5 cell viability,morphology,and proliferation were also investigated.The Ti−45Nb alloy showed no cytotoxic effect.Moreover,cells showed improved viability and adherence to the alloy surface after the laser irradiation treatment.The highest average cell viability of 115.37%was attained for the alloy laser-irradiated with 15 mJ.Results showed that the laser surface modification can be successfully utilized to significantly improve alloy performance in a biological environment.

Biocorrosion property and cytocompatibility of calcium phosphate coated Mg alloy

Calcium phosphate coated Mg alloy was prepared. The phase constitute and surface morphology were identified and observed by X-ray diffractometer （XRD） and SEM. The results show that the coating is composed of flake-like CaHPO4-2H2O crystals. The corrosion resistance of the coated Mg alloy was measured by electrochemical polarization and immersion test in comparison with uncoated Mg alloy. Cytocompatibility was designed by observing the attachment, growth and proliferation of L929 cell on both coated and uncoated Mg alloy samples. The results display that the corrosion resistance of the coated Mg alloy is better than that of uncoated one. The immersion test also shows that the calcium phosphate coating can mitigate the corrosion of Mg alloy substrate, and tends to transform into hydroxyapatite （HA）. Compared with uncoated Mg alloy, L929 cells exhibit good adherence, growth and proliferation characteristics on the coated Mg alloy, indicating that the cytocompatibility is significantly improved with the calcium phosphate coating.

Aetiopathogenesis of autoimmune hepatitis

The histological hallmark of autoimmune hepatitis（AIH） is a dense portal mononuclear cell infiltrate that invades the surrounding parenchyma and comprises T and B lymphocytes,macrophages,and plasma cells.An unknown but powerful stimulus must be promoting the formation of this massive inflammatory cellular reaction that is likely to initiate and perpetuate liver damage.An autoimmune attack can follow different pathways to inflict damage on hepatocytes.Liver damage is likely to be orchestrated by CD4^＋ T lymphocytes recognizing an autoantigenic liver peptide.To trigger an autoimmune response,the peptide must be embraced by an HLA class Ⅱ molecule and presented to naive CD4^＋ T helper（Th0） cells by professional antigen presenting cells,with the co-stimulation of ligand-ligand fostering interaction between the two cells.Th0 cells become activated,differentiate into functional phenotypes according to the cytokines prevailing in the microenvironment and the nature of the antigen,and initiate a cascade of immune reactions determined by the cytokines produced by the activated T cells.Th1 cells,arising in the presence of the macrophage-derived interleukin（IL） -12,secrete mainly IL-2 and interferon-gamma（IFN-γ）,which activate macrophages,enhance expression of HLA classⅠ（increasing liver cell vulnerability to a CD8^＋ T cell cytotoxic attack）,and induce expression of HLA class Ⅱ molecules on hepatocytes.Th2 cells,which differentiate from Th0 if the microenvironment is rich in IL-4,produce mainly IL-4,IL-10,and IL-13 which favour autoantibody production by B lymphocytes.Physiologically,Th1 and Th2 antagonize each other.Th17 cells,a recently described population,arise in the presence of transforming growth factor beta（TGF-β） and IL-6 and appear to have an important effector role in inflammation and autoimmunity.Theprocess of autoantigen recognition is strictly controlled by regulatory mechanisms,such as those exerted by CD4^＋CD25^＋ regulatory T cells,which derive from Th0 in the presence of TGF-β,but in the absence of IL-6.If regulatory mechanisms fail,the autoimmune attack is perpetuated.Over the past three decades different aspects of the above pathogenic scenario have been investigated.In particular,a defect in immunoregulation affecting CD4^＋CD25^＋ regulatory T cells（T-regs） has been demonstrated in AIH,particularly at diagnosis or during relapse.Advances in the study of autoreactive T cells have occurred mostly in AIH type 2,since the knowledge that CYP2D6 is the main autoantigen has enabled the characterization of both CD4 and CD8 T cells targeting this cytochrome.CD4 T cells from patients with type 2 AIH positive for the predisposing HLA allele DRB10701 recognize seven regions of CYP2D6,five of which are also recognized by CD8 T cells.High numbers of IFN-γ producing CD4 T cells and CD8 T cells are associated with biochemical evidence of liver damage,suggesting a combined cellular immune attack.

Comparison of nickle release and cytocompatibility between porous and dense NiTi alloy

The porous NiTi(pNiTi)samples were produced by sintering evaporation using Ti−50.8Ni(at.%)gasatomized powders.The samples were analyzed by metallographic microscope and X-ray dispersive spectroscopy(XRD).A comparison of nickel(Ni)release and cytocompatibility between pNiTi and dense NiTi(dNiTi)was made.The results showed that the pNiTi has good mechanical properties.Ni releases from pNiTi in vitro and in vivo are more serious than those form dNiTi.The proliferation and differentiation of cells cultured with the pNiTi extracting liquid are significantly worse,and the rate of early apoptosis is higher.In conclusion,pNiTi is mechanically similar to bone,but pNiTi releases more Ni and interferes with cell proliferation and differentiation.A significantly cautious approach should be adopted when using it as a medical implant.

Study on biocompatibility of PDLLA/HA/DBM with co-cultured human osteoblasts in vitro

Objective: To evaluate the osteocompatibility of D, L-polylactic/hydroxyapatite/decalcifying bone matrix (PDLLA/HA/DBM), and compare with PDLLA and DBM. Methods: Human primary osteoblasts isolated from the femoral head of patients were inoculated onto PDLLA/HA/DBM, PLA and DBM respectively. The proliferation rate and collagen Ⅰ expression were detected. The interface between biomaterial and osteoblasts was investigated with phase contrast microscopy and electron scanning microscopy. Results: Best proliferation rate was observed with the PDLLA/HA/DBM and followed by DBM and PLA, suggesting that PDLLA/HA/DBM satisfying most requirements for the cultivation of human osteoblasts. Scanning electron microscopy showed the morphology of osteoblasts was correlated with the proliferation data. The cells, well spread and flattened, were attached closely on the surface of biomaterial with an arched structure and had normal morphology. The extracellular collagenous matrixs covered the surface of biomaterial and packed the granules of biomaterial. Conclusion: PDLLA/HA/DBM can form osteointerface early and have a good biocompability.

Biocompatibility of vascular stents manufactured using metal injection molding in animal experiments

This study aimed to evaluate the feasibility and safety of a novel stent manufactured by metal injection molding(MIM)in clinical practice through animal experiments.Vessel stents were prepared using powder injection molding technology to considerably improve material utilization.The influence of MIM carbon impurity variation on the mechanical properties and corrosion resistance of 316L stainless steel was studied.In vitro cytotoxicity and animal transplantation tests were also carried out to evaluate the safety of MIM stents.The results showed that the performance of 316L stainless steel was very sensitive to the carbon content.Carbon fluctuations should be precisely controlled during MIM.All MIM stents were successfully implanted into the aortas of the dogs,and the MIM 316L stents had no significant cytotoxicity.The novel intravascular stent manufactured using MIM can maintain a stable form and structure with fast endothelialization of the luminal surface of the stent and ensure long-term patency in an animal model.The novel intravascular stent manufactured using MIM demonstrates favorable structural,physical,and chemical stability,as well as biocompatibility,offering promising application in clinical practice.

Evaluation of cellular responses associated with subcutaneous implantation of dental porcelain in a rat model

Biocompatibility of dental porcelain is of crucial importance to the long-term success of dental prostheses because of its close contact with oral tissues for extended periods. This investigation was aimed to evaluate cellular responses to locally produced dental porcelain （Universiti Sains Malaysia, Malaysia） after a short-term subcutaneous implantation in a rat model. Locally produced dental porcelains supplied in disc form were implanted subcutaneously into 12 Sprague-Dawley male albino rats, which were sacrificed in groups of 3 at 1, 2, 3 and 4 weeks after implantation. A semi-quantitative histological analysis of the tissue surrounding implanted discs was done under an image analyzer after staining with hematoxyline and eosin. The macrophage was clearly the dominant cell type at the implant surface at the first week after implantation, followed by a gradual decrease as the implantation period increased. On the contrary, fibroblasts and fibrocytes were the dominant cell types in the tissue surrounding the implanted discs at the third and fourth week after implantation with the appearance of mature collagen. From pathological point of view, the disappearance of inflammatory cellular responses and the well matured fibrous connective tissue surrounding the implanted discs indicate a satisfactory in vivo biocompatibility.

Comparison of human amniotic fluid-derived and umbilical cord Wharton＇s Jelly-derived mesenchymal stromal cells： Characterization and myocardial differentiation capacity

Objective To compare the characterization and myocardial differentiation capacity of arnniotic fluid-derived mesenchymal stromal cells （AF MSCs） and umbilical cord Wharton＇s Jelly-derived mesenchymal stromal cells （WJ MSCs）. Methods The human AF MSCs were cultured from amniotic fluid samples obtained by amniocentesis. The umbilical cord WJ MSCs were obtained from Wharton＇s Jelly of umbilical cords of infants delivered full-term by normal labor. The morphology, growth curves, and analyses by flow cytometry of cell surface markers were compared between the two types of cells. Myocardial genes （GATA-4, c-TnT, a-actin, and Cx43） were detected by real-time PCR and the corresponding protein expressions were detected by Western blot analysis after myocardial induced in AF MSCs and WJ MSCs. Results Our findings revealed AF MSCs and WJ MSCs shared similar morphological characteristics of the fibroblastoid shape. The AF MSCs were easily obtained than the WJ MSCs and had a shorter time to reach adherence of 2.7 ± 1.6 days to WJ MSCs of 6.5 ± 1.8 days. The growth curves by MTT cytotoxic assay showed the AF MSCs had a similar proliferative capacity at passage 5 and passage 10. However, the proliferative capacities ofWJ MSCs were decreased at 5 passage relative to 10 passage. Both AF stem cells and WJ stem cells had the characteristics of mesenchymal stromal cells with some characteristics of embryonic stem cells. They express CD29 and CD105, but not CD34. They were positive for Class I major histocompatibility （MHC I） antigens （HLA-ABC）, and were negative, or mildly positive, for MHC Class II （HLA-DR） antigen. Oct-4 was positive in all the two cells types. Both AF MSCs and WJ MSCs could differentiate along myocardium. The differentiation capacities were detected by the expression of GATA-4, c-TnT, a-actin, Cx43 after myocardial induction. Conclusions Both AF MSCs and WJ MSCs have the potential clinical application for myogenesis in cardiac regenerative therapy.

ENDOGENOUS EXPRESSION AND HLA STABILIZATION ASSAY OF PLASMODIUM FALCIPARUM CTL EPITOPE MINIGENE IN HUMAN HLA- A2.1 AND HLA- B51 CELLS

To evaluate the Plasmodium falciparum CTL epitope vaccines in HLA class I allele specific human cell lines that have high frequency among Chinese population. Methods. Synthesized oligonucleotides encoding for P.f. CTL epitope genes, constructed eukaryotic expression plasmids, transfected the minigenes into HLA class I allele specific human cell lines and identified endogenous expressing of the minigenes by RT- PCR and HLA stabilization assay. Results. Two mini- genes encoding Plasmodium falciparum CTL epitopes were designed and cloned, respectively, into an eukaryotic expressing vector to form TR26 which was restricted to HLA- B51, SH6 which was restricted to HLA- A2.1, and TS, which had the two aforementioned mini- genes fused in tandem. All of these CTL epitope genes were transfected and endogenously expressed in respective cell lines containing appropriate HLA molecules. The obviously increased expressions of HLA class I molecules were detected in the transfected cell lines. It was demonstrated that the two discrete Plasmodium falciparum epitope genes were effectively processed and presented, and the close proximity of the two epitope genes in one chain as in mini- gene TS did not interfere with the processing and presenting of each epitope gene in corresponding cell line. Conclusion. A successful expression and presentation of multiple CTL epitope mini- gene in MHC class I allele specific human cell lines were demonstrated by an in vitro assay, which could be corresponding to the vaccination of CTL vaccines in people with different MHC I molecules. This work also suggested the possibility of constructing a multiple CTL epitope plasmodium falciparum DNA vaccine that could cover most of Chinese population.

Study on Biocompatibility of Cross-linked Hyaluronic Acid Derivatives

Objective:The cross-linked production,which was prepared by HA and cross-linking agent STMP,EDC,GP through cross-linking reaction,might be used in drug delivery system(DDS).To ensure the security of clinical application,the excellent properties such as none cell toxicity,nonirritant,none general toxicity,none immunological rejection are necessary.Methods:In accordance with the request of GB/T 16886.1 on security evaluation of medical biomaterials,cell toxicity test,hemolysis test,intracutaneous stimulation test,acute toxicity test,and hypersensitive test were required.Results:Cell toxicity of HA-STMP,HA-EDC,HA-GP were all less than 1.All hypersensitive tests were eligible.But HA-EDC,HA-GP produced different degrees of slight thrill,slight toxicity,hemolysis rate,which were larger than the standard value.Conclusion:HA-STMP possesses favourable biocompatibility,which is a kind of ideal biomaterials and drug carriers.

Hemocompatibility and cytocompatibility of diblock copolymer poly(2-ethyl-2-oxazoline)-poly(D,L-lactide)-based micelles

A synthetic diblock copolymer poly（2-ethyl-2-oxazoline）-poly（D,L-lactide） （PEOz-PLA） can self-assemble into micelles with an increased efficiency of drug delivery. However, the interactions of blood-micelles and cell-micelles remain unclear. In the present study, we aimed to assess the hemocompatibility and cytocompatibility of PEOz-PLA micelles in order to clarify its potentials as carriers for drug delivery. Blood compatibility of the micelles was evaluated by hemolysis analysis, coagulation test, platelet activation investigation and assessment of their interaction with protein. The results revealed that PEOz-PLA micelles had a favorable blood compatibility. In addition, PEOz-PLA micelles showed a good cytocompatibility through SRB assay, presenting only negligible cytotoxicity when incubated with KBv cells. Taken together, PEOz-PLA micelles could be used as a hemocompatible and cytocompatible drug carrier for intravenous administration.

Double network hydrogel with high mechanical strength:Performance,progress and future perspective

With high water content(～90 wt%) and significantly improved mechanical strength(～MPa),double network(DN) hydrogels have emerged as promising biomaterials with widespread applications in biomedicine.In recent years,DN hydrogels with extremely high mechanical strength have achieved great advance,and scientists have designed a series of natural and biomimetic DN hydrogels with novel functions including low friction,low wear,mechanical anisotropy and cell compatibility.These advances have also led to new design of biocompatible DN hydrogels for regeneration of tissues such as cartilage.In this paper,we reviewed the strategies of designing high-strength DN hydrogel and analyzed the factors that affect DN hydrogel properties.We also discussed the challenges and future development of the DN hydrogel in view of its potential as biomaterials for their biomedical applications.

In vitro and in vivo studies on as-extruded Mg-5.25wt.%Zn-0.6wt.%Ca alloy as biodegradable metal

Magnesium alloys have shown prospective applications as a new biodegradable metal within bone. To garantee the longterm biocompatibility, a Mg-Zn-Ca alloy,composing of essential elements for human, was prepared and its feasibility for orthopedic applications was investigated. The in vitro and in vivo corrosion of Mg-Zn-Ca alloy as well as the biocompatibility were studied. The in vitro corrosion tests in five kinds of physiological solutions showed that the corrosion rates and corrosion morphologies of the alloy were strongly influenced by the solution used. The addition of serum in Hank’s and MEM significantly slowed down the corrosion rate and improved the corrosion uniformity of the alloy. The corrosion rate decreased with increasing serum concentration.The alloy showed the slowest corrosion rate as well as homogeneous corrosion morphology in MEM＋10%FBS. Both the indirect and direct cell experiments indicated good cytocompatibility of the extruded Mg-Zn-Ca alloy. In vivo, we observed a gradual degradation process from the surface of extruded Mg-Zn-Ca alloy and only 40% in volume of implant was left after 4 weeks implantation in medullary cavities of mice. The micro-CT and histological analyses revealed its good biocompatibility with peri-implant new bone formation and increasing cortical bone thickness with increasing implantation period. This study showed that the extruded MgZn-Ca alloy provided sufficient biocompatibility for orthopedic application, though the in vivo corrosion rate should be further reduced for clinical use.

Corrosion resistance and cytocompatibility of Ti-20Zr-10Nb-4Ta alloy surface modified by a focused fiber laser

The corrosion resistance and cytocompatibility of Ti-20 Zr-10 Nb-4 Ta（TZNT） alloy modified by surface laser treatment were investigated. The scanning electron microscopy（SEM） measurements indicated that laser treatment on TZNT alloy generated groove morphologies with the width of^40 μm and the depth of ~10 μm on the surface. The water contact angles along the groove direction decreased by 51%compared with that of the untreated alloy. The laser treatment promoted the oxidation of metallic Ti, Zr and Nb and produced more stable oxides on surface. The corrosion potential increased by 50% and corrosion current density decreased by72% compared with that of the untreated alloy in the anodic polarization test for the alloy in Hank’s solution at 37°C. This indicated the improvement of the corrosion resistance by laser treatment. The cytotoxicity testing results showed that the laser-treated TZNT alloy performed similar MC3 T3-E1 cell viability compared with the untreated alloy. The cells displayed oriented growth along the groove direction due to the increased hydrophilicity. This novel material may be a new candidate in orthopedics and dentistry implantations fields.

Experimental study on the adhesion, migration and three-dimensional growth of Schwann cells on absorbable biological materials

OBJECTIVE: To study the adhesion, migration and three-dimentional growth of Schwann cells on PLA (polylactic acid) nonspinning fibre cloth and polyglycolic/polylactic acid (PLGA) fibres. METHODS: Schwann cells/ECM gel solution and PLA nonspinning fibre cloth and PLGA fibres pretreated by collagen, polylysine and ECM were co-cultured. Then the migration and three-dimensional growth of Schwann cells on the fibres were observed under phase contrast microscope and laser scanning confocal microscope. RESULTS: Schwann cell/ECM solution was compounded with PLA nonspinning fibre cloth. With formation of gel, most Schwann cells resided in the fibre net holes, and adhered to the fibres to form a multiplayer-arranged Schwann cell column like Bungner band. Schwann cells could adhere to PLGA fibres and grew and migrated along the fibres. ECM gel could significantly increase the adhering and migrating cell number. CONCLUSIONS: ECM gel can facilitate the adhesion, growth and migration of Schwann cells on the seteroframe. It is a good integrating material for tissue engineering bioartificial nerve.

Electrochemical behaviour and cytocompatibility of nano-fluoridated apatite coating on biodegradable magnesium alloy by simple chemical conversion

Magnesium and its alloys have attracted great attention as biocompatible and degradable biomaterials recent years.But their corrosion rate has been proved to be too high,which limits their biomedical application greatly.In order to improve the corrosion resistance,nano-fluoridated apatite(FA) coating was prepared on ZK60 magnesium alloy by a simple chemical conversion method.The FA coating showed a needle-like morphology.The polarization curves and EIS plots indicated that the FA coating improved the corrosion potential by 125 mV and doubled the polarization resistance of the magnesium alloy,meanwhile decreasing the corrosion current by two orders of magnitude of the substrate in simulated body fluid.The MTT assay indicated good cytocompatibility of L-929 cells with the fluoridated apatite coated magnesium alloy.

In vitro and in vivo cytocompatibility evaluation of biodegradable magnesium-based stents: a review

Biodegradable magnesium（Mg）-based vascular stents have been designed as temporary scaffolds to treat angiostenotic lesions for the maintenance of normal blood flow.Numerous studies have presented in vitro and in vivo tests for the evaluation of the safety and feasibility of Mg-based vascular stents and the related materials. Therein the cytocompatibility is a basic and important parameter in the evaluation system. In this review, we summarize the applications and limitations of in vitro evaluation methods including basic characterization methods and direct and indirect cytotoxicity tests. We discuss the influencing factors on cytotoxicity, such as surface roughness, preconditioning of sample surface, cell type for the biocompatibility evaluation in direct contact as well as conditions for the formation of extracts/degradation products for indirect assays. Besides, we highlight the recent in vivo animal tests and clinical trials about Mgbased stents along with some associated results. The aim of this review is to provide a meaningful reference in the further developments and related evaluation methods of Mg-based stents.

Biocompatibility of nano-hydroxyapatite/Mg-Zn-Ca alloy composite scaffolds to human umbilical cord mesenchymal stem cells from Wharton's jelly in vitro

Seeding cells and scaffolds play pivotal roles in bone tissue engineering and regenerative medicine.Wharton’s jelly-derived mesenchymal stem cells(WJCs)from human umbilical cord represent attractive and promising seeding cells in tissue regeneration and engineering for treatment applications.This study was carried out to explore the biocompatibility of scaffolds to seeding cells in vitro.Rod-like nano-hydroxyapatite(RN-HA)and flake-like micro-hydroxyapatite(FM-HA)coatings were prepared on Mg-Zn-Ca alloy substrates using micro-arc oxidation and electrochemical deposition.WJCs were utilized to investigate the cellular biocompatibility of Mg-Zn-Ca alloys after different surface modifications by observing the cell adhesion,morphology,proliferation,and osteoblastic differentiation.The in vitro results indicated that the RN-HA coating group was more suitable for cell proliferation and cell osteoblastic differentiation than the FM-HA group,demonstrating better biocompatibility.Our results suggested that the RN-HA coating on Mg-Zn-Ca alloy substrates might be of great potential in bone tissue engineering.