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Effect of mucosa thicknesses on stress distribution of implant-supported overdentures under unilateral loading: Photoelastic analysis 单侧载荷下粘膜厚度对种植覆盖义齿应力分布的影响:光弹性分析
Pub Date : 2019-10-01 DOI: 10.1177/2280800019882645
O. Ozyilmaz, F. Aykent, Gulsum Sayin Ozel
Introduction: The aim of this study was to evaluate the effect of different heights of attachment and mucosa thicknesses on the stress distribution of two implant-retained mandibular overdenture designs under loading using the photoelastic stress analysis method. Materials and methods: Six photoelastic models of an edentulous mandibula were fabricated with two solitary implants that were placed in the canine regions. The attachment systems studied were ball and locator stud attachments. Both the ball and locator groups included three models that had different residual ridge heights so as to provide different mucosa thicknesses (1 mm–1 mm, 1 mm–2 mm, 1 mm–4 mm). A static vertical force of 135 N was applied unilaterally (each on the right then the left side) to the central fossa of the first molars. Models were positioned in the field of a circular polariscope to observe the distribution of isochromatic fringes around the implants and the interimplant areas under loading. The photoelastic stress fringes were monitored and recorded photographically. Results: The ball attachment groups showed higher stress values than did the locator groups under loading. Both attachment systems produced the lowest stress values in stimulated 1 mm–1 mm mucosa thickness models. The models with 1 mm–2 mm mucosa thicknesses showed higher stress values than did other models for both attachment systems. The highest stress value observed around both attachment systems was the moderate level in all test models. Conclusion: In different height mucosa thicknesses, locator attachment models distributed the load to the other side of the implant and its surrounding tissue, whereas the ball attachment did not. Regardless of mucosal thickness and attachment type, the implant on the loading side was subjected to the highest stress concentration.
摘要:本研究采用光弹性应力分析方法,评价不同附着体高度和黏膜厚度对两种种植体下颌覆盖义齿在载荷作用下应力分布的影响。材料与方法:采用两颗单体种植体植入犬齿区,制作了6个无牙下颌光弹性模型。所研究的附件系统为滚珠和定位螺柱附件。球组和定位器组均包括三种模型,这些模型具有不同的残余脊高,从而提供不同的粘膜厚度(1 mm - 1 mm, 1 mm - 2 mm, 1 mm - 4 mm)。在第一磨牙中央窝单侧施加135牛的静态垂直力(分别在右侧和左侧)。将模型放置在圆形偏光镜视野中,观察载荷作用下植入体周围和植入体间等色条纹的分布。光弹性应力条纹的监测和照相记录。结果:在载荷作用下,球附着组的应力值高于定位器组。在受刺激的1 mm - 1 mm粘膜厚度模型中,两种附着系统产生的应力值最低。两种附着系统中,厚度为1 mm ~ 2 mm的模型均表现出较高的应力值。在所有测试模型中,两种依恋系统的最高应力值均为中等水平。结论:在不同高度粘膜厚度下,定位器附着体模型将载荷分配到种植体的另一侧及其周围组织,而球附着体则没有。无论粘膜厚度和附着类型如何,加载侧种植体承受的应力浓度最高。
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引用次数: 4
Enhanced antibacterial activity of titanium by surface modification with polydopamine and silver for dental implant application 聚多巴胺和银表面修饰增强钛在种植牙中的抗菌活性
Pub Date : 2019-07-01 DOI: 10.1177/2280800019847067
S. Choi, Y. Jang, Jong-Hwa Jang, T. Bae, Sook-Jeong Lee, Min-Ho Lee
Background: Biofilm formation and microbial colonization on the surface of implant devices may cause dental caries and peri-implantitis. Therefore, various surface treatments have been developed to improve the antibacterial activity of titanium implant. Methods: Silver-loaded polydopamine coating was formed by immersing pure titanium in dopamine hydrochloride/HCl buffer solution for 24 h in 50 mL silver nitrate solutions with different concentrations for 30 min. Microbial growth inhibition and microbial growth curve analyses for bacterial solutions of Streptococcus mutans and Porphyromonas gingivalis incubated with the specimens were respectively conducted by counting the numbers of colonies on agar solid medium and by measuring absorbance using enzyme-linked immunosorbent assay reader. Results: Silver nanoparticles were uniformly distributed over the whole surface of the polydopamine and silver-coated titanium specimens. The numbers of microbial colonies for both bacteria cultured with surface-modified titanium were significantly lower than those cultured with uncoated titanium. When Streptococcus mutans and Porphyromonas gingivalis were cultured with surface-modified titanium, the lag phase of the growth curves for both bacteria was continually maintained, whereas the lag phase for Streptococcus mutans and Porphyromonas gingivalis changed to exponential phase after 9 and 15 h, respectively, when both bacteria were cultured with uncoated titanium. Conclusion: It was confirmed that the coating of polydopamine and silver on the surface of titanium effectively retards the microbial growth, which can cause the formation of biofilm and pathogenesis of gum disease in the mouth.
背景:种植体表面的生物膜形成和微生物定植可能导致龋齿和种植体周围炎。因此,人们开发了各种表面处理方法来提高钛植入物的抗菌活性。方法:将纯钛浸泡在盐酸多巴胺/盐酸缓冲液中,在50 mL不同浓度的硝酸银溶液30分钟。通过计数琼脂固体培养基上的菌落数和使用酶联免疫吸附测定仪测量吸光度,分别对与样品一起孵育的变形链球菌和牙龈卟啉单胞菌的细菌溶液进行微生物生长抑制和微生物生长曲线分析。结果:银纳米粒子均匀分布在聚多巴胺和镀银钛样品的整个表面。用表面修饰的钛培养的两种细菌的微生物菌落数均显著低于用未涂覆的钛培养。当用表面修饰的钛培养变形链球菌和牙龈卟啉单胞菌时,两种细菌的生长曲线的滞后期持续保持,而当用未涂覆的钛培养这两种细菌时,变形链球菌和齿龈卟啉单胞杆菌的滞后期分别在9和15小时后变为指数期。结论:钛表面的聚多巴胺和银涂层有效地延缓了微生物的生长,从而导致口腔中生物膜的形成和牙龈疾病的发病机制。
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引用次数: 41
Antimicrobial activity of endodontic sealers and medications containing chitosan and silver nanoparticles against Enterococcus faecalis 含壳聚糖和银纳米颗粒的根管封闭剂和药物对粪肠球菌的抗菌活性
Pub Date : 2019-07-01 DOI: 10.1177/2280800019851771
J. Loyola-Rodríguez, Fernando Torres-Méndez, L. F. Espinosa-Cristóbal, J. García-Cortés, Alejandra Loyola-Leyva, F. J. González, Uriel Soto-Barreras, R. Nieto-Aguilar, G. Contreras-Palma
Background: The main microorganism associated with the failure of endodontic treatments is Enterococcus faecalis. Although several endodontic therapeutics have demonstrated antimicrobial activity against E. faecalis, the antimicrobial effectiveness of chitosan (CsNPs) and silver nanoparticles (AgNPs) included into conventional endodontic sealers for endodontic therapies is still unclear. Aim: The objective of this study was to evaluate the antibacterial activity increment (AAI) of endodontic sealers containing CsNPs and AgNPs as well as some chemical components against E. faecalis by direct contact assays. Methods: CsNPs and AgNPs were synthesized by reduction and ionic gelation methods, respectively. Nanoparticles were characterized by dynamic light scattering and energy dispersive X-ray analysis. The bactericidal activity was tested on monolayers on agar plates and collagen membrane surface assays against E. faecalis. Results: The size of CsNPs was 70.6±14.8 nm and zeta potential was 52.0±5.4 mV; the size of AgNPs was 54.2±8.5 nm, and zeta potential was –48.4±6.9 mV. All materials, single or combined, showed an AAI, especially when CsNPs, chlorhexidine (Chx), and the combination of CsNPs-Chx were added. However, the combination of CsNPs-Chx showed the highest (55%) AAI, followed by Chx (35.5%) and CsNPs (11.1%), respectively. There was a significant statistical difference in all comparisons (p < 0.05). Tubliseal (40%) and AH Plus (32%) sealants showed a higher AAI on E. faecalis in the monolayer test and collagen membrane assay analyzed by scanning electron microscopy. Conclusions: Tubliseal and AH plus sealers combined with nanoparticles, especially CsNPs-Chx, could be used for conventional endodontic treatments in the control of E. faecalis bacteria.
背景:与牙髓治疗失败相关的主要微生物是粪肠球菌。尽管几种根管治疗方法已证明对粪肠球菌具有抗菌活性,但用于根管治疗的传统根管封闭剂中包含的壳聚糖(CsNPs)和银纳米颗粒(AgNPs)的抗菌效果仍不清楚。目的:本研究的目的是通过直接接触法评估含有CsNPs和AgNPs以及一些化学成分的根管封闭剂对粪肠球菌的抗菌活性增量(AAI)。方法:分别采用还原法和离子凝胶法合成CsNPs和AgNPs。通过动态光散射和能量色散X射线分析对纳米颗粒进行了表征。在琼脂平板上的单层上测试杀菌活性,并对粪大肠杆菌进行胶原膜表面测定。结果:CsNPs的尺寸为70.6±14.8nm,ζ电位为52.0±5.4mV;AgNPs的尺寸为54.2±8.5 nm,ζ电位为–48.4±6.9 mV。所有材料,无论是单一材料还是组合材料,都显示出AAI,尤其是当添加CsNPs、氯己定(Chx)和CsNPs-Chx的组合时。然而,CsNPs-Chx的组合显示出最高的AAI(55%),其次是Chx(35.5%)和CsNPs(11.1%)。在所有比较中都存在显著的统计学差异(p<0.05)。在单层测试和扫描电子显微镜分析的胶原膜分析中,Tublisal(40%)和AH-Plus(32%)密封剂对粪便大肠杆菌显示出更高的AAI。结论:管状和AH+封闭剂与纳米颗粒,特别是CsNPs-Chx相结合,可用于常规牙髓治疗,以控制粪便大肠杆菌。
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引用次数: 37
HA-based dermal filler: downstream process comparison, impurity quantitation by validated HPLC-MS analysis, and in vivo residence time study 基于ha的真皮填充剂:下游工艺比较,通过有效的HPLC-MS分析进行杂质定量,以及体内停留时间研究
Pub Date : 2019-07-01 DOI: 10.1177/2280800019867075
C. Guarise, Carlo Barbera, M. Pavan, S. Panfilo, R. Beninatto, D. Galesso
The success of hyaluronic acid (HA)-based dermal fillers, with more than 2 million minimally invasive procedures conducted in 2016 in the US alone, is due to their hygroscopic properties of biocompatibility and reversibility. The type and density of HA cross-linkage, as well as the manufacturing technology, may influence not only the in vivo persistence but also the safety profile of dermal fillers. 1,4-Butanediol diglycidyl ether (BDDE) is the cross-linker used in most market-leading HA fillers; 1,4-butanediol di-(propan-2,3-diolyl) ether (BDPE) is the major impurity obtained from the HA–BDDE cross-linking (HBC) process. In this work, a new process to obtain high purity HBC fillers was developed. A new HPLC-MS method was validated for the quantification of BDPE content in HBC dermal fillers. In vitro cytotoxicity of BDPE was evaluated in fibroblasts (IC50 = 0.48 mg/mL). The viscoelasticity was monitored during the shelf-life of the HBC-10% hydrogel and was correlated with in vitro hyaluronidase resistance and in vivo residence time in a rabbit model. This analysis showed that elasticity is the best parameter to predict the in vivo residence time. Finally, a series of parameters were investigated in certain marketed dermal fillers and were compared with the results of the HBC-10% hydrogel.
基于透明质酸(HA)的真皮填充物的成功,仅2016年在美国就进行了200多万次微创手术,这是由于它们具有生物相容性和可逆性的吸湿特性。HA交联的类型和密度,以及制造技术,不仅可能影响真皮填充物的体内持久性,还可能影响其安全性。1,4-丁二醇二缩水甘油醚(BDDE)是大多数市场领先的HA填料中使用的交联剂;1,4-丁二醇二(丙-2,3-二醇)醚(BDPE)是HA–BDDE交联(HBC)过程中获得的主要杂质。本工作开发了一种获得高纯度HBC填料的新工艺。验证了一种新的HPLC-MS方法用于HBC真皮填充物中BDPE含量的定量。在成纤维细胞中评估BDPE的体外细胞毒性(IC50=0.48mg/mL)。在HBC-10%水凝胶的保质期内监测粘弹性,并在兔模型中与体外透明质酸酶耐药性和体内停留时间相关。该分析表明,弹性是预测体内停留时间的最佳参数。最后,在某些市场上销售的真皮填充物中研究了一系列参数,并与HBC-10%水凝胶的结果进行了比较。
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引用次数: 14
Facile preparation of UV-cured polymer sealants encapsulated graphene nanofillers and evaluation of their water vapor permeability 紫外线固化聚合物密封剂封装石墨烯纳米填料的简易制备及其水蒸气渗透性评价
Pub Date : 2019-04-01 DOI: 10.1177/2280800019833561
K. Uma, Yi‐Ru Lee, Gung-Tin Pan, T. C. Yang
Background: Due to the outstanding properties of graphene, researchers are considering it a good candidate for thin film encapsulation on polymer substrates. In this work, we produce a UV-cured resin prepared by an inexpensive solution technique for the encapsulation of graphene oxide (GO), mechanical exfoliation graphene (mG), reduced graphene oxide (rGO), graphite, and SiO2 nanofillers on the surface of a PET film for employment as an impermeable film. Methods: The water vapor transmission rate (WVTR) is measured for the UV-cured encapsulated nanofillers on PET films. Results: The WVTR was reduced to <10−2 g m−2/day for GO and rGO nanofillers with a thickness of 1 mm. Pencil scratch hardness tests performed on the encapsulated nanofillers deposited on the PET film showed them to be stable up to 5H–8H and the glass transition temperature results for the GO, mG, and rGO nanofillers on PET remained steady up to 180°C. Conclusions: The prepared UV-cured resin encapsulated graphene nanofillers coated on the polymer substrate by a simple solution method was shown to have good impermeability to water vapor.
背景:由于石墨烯的优异性能,研究人员认为它是在聚合物基底上进行薄膜封装的良好候选者。在这项工作中,我们生产了一种紫外线固化树脂,该树脂通过一种廉价的溶液技术制备,用于在PET膜表面封装氧化石墨烯(GO)、机械剥离石墨烯(mG)、还原石墨烯(rGO)、石墨和SiO2纳米填料,用作不渗透膜。方法:测定紫外光固化PET薄膜上包封纳米填料的水蒸气透过率。结果:厚度为1 mm的GO和rGO纳米填料的WVTR降低至<10−2 g m−2/天。对沉积在PET膜上的封装纳米填料进行的铅笔划痕硬度测试表明,它们在5H–8H下保持稳定,PET上GO、mG和rGO纳米填料的玻璃化转变温度结果在180°C下保持稳定。结论:采用简单溶液法在聚合物基体上制备的紫外光固化树脂包封石墨烯纳米填料具有良好的抗水蒸气性能。
{"title":"Facile preparation of UV-cured polymer sealants encapsulated graphene nanofillers and evaluation of their water vapor permeability","authors":"K. Uma, Yi‐Ru Lee, Gung-Tin Pan, T. C. Yang","doi":"10.1177/2280800019833561","DOIUrl":"https://doi.org/10.1177/2280800019833561","url":null,"abstract":"Background: Due to the outstanding properties of graphene, researchers are considering it a good candidate for thin film encapsulation on polymer substrates. In this work, we produce a UV-cured resin prepared by an inexpensive solution technique for the encapsulation of graphene oxide (GO), mechanical exfoliation graphene (mG), reduced graphene oxide (rGO), graphite, and SiO2 nanofillers on the surface of a PET film for employment as an impermeable film. Methods: The water vapor transmission rate (WVTR) is measured for the UV-cured encapsulated nanofillers on PET films. Results: The WVTR was reduced to <10−2 g m−2/day for GO and rGO nanofillers with a thickness of 1 mm. Pencil scratch hardness tests performed on the encapsulated nanofillers deposited on the PET film showed them to be stable up to 5H–8H and the glass transition temperature results for the GO, mG, and rGO nanofillers on PET remained steady up to 180°C. Conclusions: The prepared UV-cured resin encapsulated graphene nanofillers coated on the polymer substrate by a simple solution method was shown to have good impermeability to water vapor.","PeriodicalId":51074,"journal":{"name":"Journal of Applied Biomaterials & Biomechanics","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46696398","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Research on corrosion behavior and biocompatibility of a porous Mg–3%Zn/5%β-Ca3(PO4)2 composite scaffold for bone tissue engineering Mg-3%Zn /5%β-Ca3(PO4)2多孔骨组织工程复合支架的腐蚀行为及生物相容性研究
Pub Date : 2019-04-01 DOI: 10.1177/2280800019857064
Mingying Tang, Yangjun Yan, Jianan Ouyang, Kun Yu, Congcong Liu, Xiaohua Zhou, Zhenting Wang, Youwen Deng, C. Shuai
Background: Rapid corrosion rates are a major impediment to the use of magnesium alloys in bone tissue engineering despite their good mechanical properties and biodegradability. Zinc is a promising alloy element, and it is an effective grain refiner for magnesium. β-Ca3(PO4)2 (β-TCP) is widely used for bone regeneration because of its good biocompatibility, and it also has a similar chemical and crystal structure to human bone. Methods: In this research, the magnesium alloy was reinforced by adding 3%Zn (wt.%) and 5%β-TCP (wt.%) particles in order to improve the corrosion resistance and biocompatibility. Furthermore, the biomaterial was prepared through powder metallurgy technology using NH4HCO3 as space-holding particles to construct porous Mg–3%Zn/5%β-TCP scaffolds. Results: The results revealed that the magnesium-zinc phase and calcium phosphate phase were uniformly distributed in the α-magnesium matrix. Mechanical and corrosion tests indicated that the scaffolds had mechanical strengths similar to that of human bone, and their corrosion resistance decreased with an increase in the porosity. The scaffolds had cytotoxicity grades of 0–1 against MG63 cells, SaoS2 cells, and HK-2 cells, which suggested that they were appropriate for cellular applications. In addition, the scaffolds demonstrated excellent biocompatibility when tested in rabbits. Conclusions: These results indicate that porous Mg–3%Zn/5%β-TCP scaffolds are promising biodegradable implants for bone tissue engineering.
背景:尽管镁合金具有良好的机械性能和生物降解性,但快速腐蚀速率是阻碍其在骨组织工程中使用的主要障碍。锌是一种很有前途的合金元素,是镁的有效晶粒细化剂。β-Ca3(PO4)2(β-TCP)因其良好的生物相容性而被广泛用于骨再生,并且具有与人骨相似的化学结构和晶体结构。方法:在镁合金中加入3%的Zn(wt.%)和5%的β-TCP(wt.%%)颗粒进行增强,以提高镁合金的耐腐蚀性和生物相容性。此外,通过粉末冶金技术制备了该生物材料,使用NH4HCO3作为空间保持颗粒来构建多孔Mg–3%Zn/5%β-TCP支架。结果:镁-锌相和磷酸钙相在α-镁基体中分布均匀。力学和腐蚀测试表明,支架具有与人骨相似的机械强度,并且其耐腐蚀性随着孔隙率的增加而降低。支架对MG63细胞、SaoS2细胞和HK-2细胞的细胞毒性等级为0–1,这表明它们适合细胞应用。此外,在兔子身上测试时,支架显示出良好的生物相容性。结论:这些结果表明,多孔Mg-3%Zn/5%β-TCP支架是骨组织工程中有前途的可生物降解植入物。
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引用次数: 2
Minocycline-loaded calcium polyphosphate glass microspheres as a potential drug-delivery agent for the treatment of periodontitis 二甲胺四环素负载的聚磷酸钙玻璃微球作为治疗牙周炎的潜在药物递送剂
Pub Date : 2019-04-01 DOI: 10.1177/2280800019863637
I. Gibson, A. Momeni, M. Filiaggi
Background: Periodontitis is an inflammatory disease with a bacterial etiology that affects the supporting structures of the teeth and is a major cause of tooth loss. The objective of this study was to investigate the drug loading and in vitro release of minocycline from novel calcium polyphosphate microspheres intended for use in treating periodontitis. Methods: Calcium polyphosphate coacervate, produced by a precipitation reaction of calcium chloride and sodium polyphosphate solutions, was loaded with minocycline and subsequently used to produce microspheres by an emulsion/solvent extraction technique. Microspheres classified by size were subjected to a 7-day elution in a Tris-buffer solution under dynamic conditions. The physicochemical characteristics of the drug-loaded microspheres were investigated using scanning electron microscopy, particle size analysis, Phosphorus-31 Nuclear Magnetic Resonance spectroscopy, and Inductively Coupled Plasma Optical Emission Spectroscopy. Drug loading and release were determined using ultraviolet -visible (UV/VIS) spectrophotometry. Results: Minocycline-loaded calcium polyphosphate microspheres of varying size were successfully produced, with small and large microspheres having volume mean diameters of 22 ± 1 µm and 193 ± 5 µm, respectively. Polyphosphate chain length and calcium to phosphorus mole ratio remained stable throughout microsphere production. Drug loading was 1.64 ± 0.16, 1.35 ± 0.55, and 0.84 ± 0.14 weight% for the coacervate and large and small microspheres, respectively, corresponding to mean encapsulation efficiencies of 81.7 ± 12.2 % and 50.9 ± 3.9 % for the large and small microspheres. Sustained drug release was observed in vitro over a clinically relevant 7-day period, with small and large microspheres exhibiting similar elution profiles. Antibiotic release generally followed microsphere degradation as measured by Ca and P ion release. Conclusions: This study demonstrated successful drug loading of calcium polyphosphate microspheres with minocycline. Furthermore, in vitro sustained release of minocycline over a 7-day period was observed, suggesting potential utility of this approach for treating periodontitis.
背景:牙周炎是一种细菌性病因的炎症性疾病,影响牙齿的支撑结构,是导致牙齿脱落的主要原因。本研究的目的是研究用于治疗牙周炎的新型聚磷酸钙微球中米诺环素的载药量和体外释放。方法:将氯化钙和聚磷酸钠溶液沉淀反应制备的聚磷酸钙凝聚层与米诺环素负载,然后通过乳液/溶剂萃取技术制备微球。在动态条件下,在Tris缓冲溶液中对按大小分类的微球进行7天洗脱。利用扫描电子显微镜、粒度分析、磷-31核磁共振光谱和电感耦合等离子体发射光谱对载药微球的物理化学特性进行了研究。采用紫外-可见分光光度法测定药物的载药量和释放度。结果:成功制备了不同大小的米诺环素负载聚磷酸钙微球,其中小微球和大微球的体积平均直径分别为22±1µm和193±5µm。聚磷酸盐链长和钙磷摩尔比在整个微球生产过程中保持稳定。凝聚层和大小微球的载药量分别为1.64±0.16、1.35±0.55和0.84±0.14重量%,对应于大小微球的平均包封率分别为81.7±12.2%和50.9±3.9%。在体外观察到药物在临床相关的7天内持续释放,大小微球表现出相似的洗脱特征。通过Ca和P离子释放测定,抗生素释放通常遵循微球降解。结论:本研究证明了米诺环素复合聚磷酸钙微球的载药成功。此外,观察到米诺环素在7天内的体外持续释放,这表明这种方法在治疗牙周炎方面具有潜在的实用性。
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引用次数: 14
Comparison of the microstructure and properties of a series of Mg-Zn metallic devices on biomedical applications 生物医学应用中一系列镁锌金属器件的微观结构和性能比较
Pub Date : 2019-04-01 DOI: 10.1177/2280800019842150
Taozhou Zhang, Yilong Dai, Yangjun Yan, Yu Zhang, Kun Yu, Hui Liu, Hong-jie Fang, Xier Luo, Li Li
Magnesium alloys have been investigated as biodegradable metallic materials because of their good biocompatibility with natural bone, while zinc has basic safety properties for biomedical applications and is one of the nutritionally essential elements for the human body. The microstructures and properties of some novel designs of bio-Mg-Zn alloys are studied to provide implantations which have an improvement in mechanical properties and corrosion resistance.
镁合金因其与天然骨具有良好的生物相容性而被研究为可生物降解的金属材料,而锌在生物医学应用中具有基本的安全性能,是人体的营养必需元素之一。研究了一些新设计的生物镁锌合金的微观结构和性能,以提供在机械性能和耐腐蚀性方面有所改善的植入物。
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引用次数: 0
Preparation and bioactivity of biodegradable β-tricalcium phosphate / calcium carbonate / phosphate bioactive glass composite porous ceramic 可生物降解β-磷酸三钙/碳酸钙/磷酸盐生物活性玻璃复合多孔陶瓷的制备及生物活性研究
Pub Date : 2019-04-01 DOI: 10.1177/2280800019847071
Wei Chen, Yan Liu, Jixiang Zhu, Miao Zhou, Xiaoming Chen
Background: At present, scaffold biomaterials with great biodegradation and biocompatibility are attracting more and more attention. Phosphate bioactive glass (PBG) without Si has been prepared successfully, with a glass transition temperature below 600°C. Calcium carbonate (CC)-based bioceramics with PBG as binder were sintered rapidly at a lower temperature. β-Tricalcium phosphate (β-TCP) has always been used to synthesize clinical ceramics due to its wonderful biocompatibility. Here, we combined the advantages of these raw materials to obtain a novel β-TCP/CC/PBG composite porous ceramic. Method: The preparation process of β-TCP/CC/PBG was optimized by controlling PBG content, NaCl ratio, sintering temperature, and holding time. Ceramic biodegradability was evaluated by soaking in a Tris-HCl buffer in vitro, and biocompatibility of the new material was indicated using CCK-8 tests and a live/dead fluorescence assay. Results: The best mechanical properties of β-TCP/CC/PBG composite porous ceramics were obtained with a PBG content of 60%, at which point the proportion of NaCl exerted the most significant influence on the density, porosity, and mechanical properties of the materials. The weight loss rate of the composite ceramics was 11.30%, which was much higher than that of β-TCP (1.41%) and hydroxyapatite (0.83%) ceramics. CCK-8 test and live/dead fluorescence assay indicated that the composite porous ceramics showed a biocompatibility similar to that of β-TCP ceramics. Conclusion: β-TCP/CC/PBG composite porous ceramics have potential applications in bone regeneration. It is hoped that the novel biomaterial developed in this study will prove useful for the repair of bone defects.
背景:目前,具有良好生物降解性和生物相容性的支架生物材料越来越受到人们的关注。成功制备了无硅磷酸盐生物活性玻璃(PBG),玻璃化转变温度低于600°C。以PBG为粘结剂的碳酸钙基生物陶瓷在较低的温度下快速烧结。β-磷酸三钙(β-TCP)具有良好的生物相容性,一直被用于合成临床陶瓷。在此,我们结合这些原料的优点,制备了一种新型的β-TCP/CC/PBG复合多孔陶瓷。方法:通过控制PBG含量、NaCl配比、烧结温度和保温时间,优化β-TCP/CC/PBG的制备工艺。通过在体外浸泡在Tris-HCl缓冲液中来评估陶瓷的生物降解性,并通过CCK-8测试和活/死荧光测定来表明新材料的生物相容性。结果:当PBG含量为60%时,β-TCP/CC/PBG复合多孔陶瓷的力学性能最佳,此时NaCl的比例对材料的密度、孔隙率和力学性能影响最大。复合陶瓷的失重率为11.30%,远高于β-TCP(1.41%)和羟基磷灰石(0.83%)陶瓷。CCK-8试验和活/死荧光分析表明,复合多孔陶瓷具有与β-TCP陶瓷相似的生物相容性。结论:β-TCP/CC/PBG复合多孔陶瓷在骨再生中具有潜在的应用前景。希望本研究中开发的新型生物材料将被证明对骨缺损的修复有用。
{"title":"Preparation and bioactivity of biodegradable β-tricalcium phosphate / calcium carbonate / phosphate bioactive glass composite porous ceramic","authors":"Wei Chen, Yan Liu, Jixiang Zhu, Miao Zhou, Xiaoming Chen","doi":"10.1177/2280800019847071","DOIUrl":"https://doi.org/10.1177/2280800019847071","url":null,"abstract":"Background: At present, scaffold biomaterials with great biodegradation and biocompatibility are attracting more and more attention. Phosphate bioactive glass (PBG) without Si has been prepared successfully, with a glass transition temperature below 600°C. Calcium carbonate (CC)-based bioceramics with PBG as binder were sintered rapidly at a lower temperature. β-Tricalcium phosphate (β-TCP) has always been used to synthesize clinical ceramics due to its wonderful biocompatibility. Here, we combined the advantages of these raw materials to obtain a novel β-TCP/CC/PBG composite porous ceramic. Method: The preparation process of β-TCP/CC/PBG was optimized by controlling PBG content, NaCl ratio, sintering temperature, and holding time. Ceramic biodegradability was evaluated by soaking in a Tris-HCl buffer in vitro, and biocompatibility of the new material was indicated using CCK-8 tests and a live/dead fluorescence assay. Results: The best mechanical properties of β-TCP/CC/PBG composite porous ceramics were obtained with a PBG content of 60%, at which point the proportion of NaCl exerted the most significant influence on the density, porosity, and mechanical properties of the materials. The weight loss rate of the composite ceramics was 11.30%, which was much higher than that of β-TCP (1.41%) and hydroxyapatite (0.83%) ceramics. CCK-8 test and live/dead fluorescence assay indicated that the composite porous ceramics showed a biocompatibility similar to that of β-TCP ceramics. Conclusion: β-TCP/CC/PBG composite porous ceramics have potential applications in bone regeneration. It is hoped that the novel biomaterial developed in this study will prove useful for the repair of bone defects.","PeriodicalId":51074,"journal":{"name":"Journal of Applied Biomaterials & Biomechanics","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45581405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Raman Imaging of Layered Soft Contact Lenses 层状软性隐形眼镜的拉曼成像
Pub Date : 2017-04-01 DOI: 10.5301/jabfm.5000329
K. Krysztofiak, Kamila Ciężar, M. Kościński
Background Daily disposable contact lenses are gaining in popularity among practitioners and wearers for the improved ocular health and subjective outcomes they offer. Recently a novel daily disposable contact lens material with water gradient technology was introduced. Delefilcon A lenses consist of a 33% water content silicone hydrogel core and an outer hydrogel layer which is totally free of silicone and contains 80% water. Methods The aim of the present study was to confirm the layered structure of delefilcon A contact lenses. Thickness of hydrogel coating on the silicone hydrogel core was assessed using Raman spectroscopy. To investigate the layered structure of the material, depth spectra of the lenses were recorded. Results The results obtained suggest that at about 6 μm a boundary between the hydrogel layer and silicone hydrogel core exists, which is in good agreement with the manufacturer's data. Conclusions Data collected in this experiment confirm a water gradient at the delefilcon A lens surface.
背景:日常使用的一次性隐形眼镜因其改善眼部健康和主观效果而在从业人员和佩戴者中越来越受欢迎。介绍了一种采用水梯度技术的新型日用一次性隐形眼镜材料。Delefilcon A镜片由含水量33%的硅酮水凝胶芯和完全不含硅酮且含有80%水的外水凝胶层组成。方法对delefilcon A隐形眼镜的层状结构进行研究。采用拉曼光谱法对硅酮水凝胶芯上的水凝胶涂层厚度进行了评价。为了研究材料的层状结构,记录了透镜的深度光谱。结果所得结果表明,水凝胶层与硅酮水凝胶芯之间存在约6 μ a的边界,这与厂家的数据吻合较好。结论本实验数据证实在delefilcon a透镜表面存在水梯度。
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引用次数: 5
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Journal of Applied Biomaterials & Biomechanics
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