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A thermodynamic discourse on the dissolution behavior of bioactive glasses 生物活性玻璃溶解行为的热力学论述
Q1 Materials Science Pub Date : 2016-01-14 DOI: 10.1515/bglass-2016-0010
Barbara Pföss, R. Conradt
Abstract The interaction between bioactive glass and body fluid is crucial for the special properties of this material, therefore a large number of experimental data is available in literature. However, a frame for systematic interpretation of these results in terms of understanding the mechanisms at the interface between glass and body medium and the relation between glass composition and dissolution behavior is still missing. For two multicomponent bioactive glasses, 45S5 and 13-93, the Gibbs energies of the glassy material on one side and their aqueous system on the other side were calculated individually. The difference between solid material and aqueous system further constitutes the pH dependent Gibbs energy of hydration, ∆Ghydr. The impact of glass compositions and glassy or crystalline state on ∆Ghydr is demonstrated referring to chemical durability. Along considerations regarding the aqueous system, the thermodynamic calculations proof the precipitation of hydroxyapatite inwater and simulated body fluid for a systemcontaining P2O5 and Ca2+. In the course of deriving the Gibbs energies for bioactive glass compositions via constitutional compounds, bioactive behavior is discussed from the point of coexisting equilibrium phases in the system of Na2O-CaO-SiO2.
生物活性玻璃与体液的相互作用是这种材料特殊性能的关键,因此文献中有大量的实验数据。然而,从了解玻璃与体介质界面的机制以及玻璃成分与溶解行为之间的关系方面,仍然缺乏一个系统解释这些结果的框架。对于45S5和13-93两种多组分生物活性玻璃,分别计算了一侧玻璃材料和另一侧水体系的吉布斯能。固体物质与水体系之间的差异进一步构成了依赖pH的水化吉布斯能∆Ghydr。玻璃成分和玻璃态或结晶态对∆Ghydr的影响参照化学耐久性进行论证。考虑到水系统,热力学计算证明了羟基磷灰石在水中的沉淀和模拟体液中含有P2O5和Ca2+的系统。在通过组成化合物推导生物活性玻璃组合物的吉布斯能的过程中,从na20 - cao - sio2体系中共存平衡相的角度讨论了生物活性行为。
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引用次数: 0
Acellular Bioactivity of Sol-Gel Derived Borate Glass-Polycaprolactone Electrospun Scaffolds 溶胶-凝胶硼酸盐玻璃-聚己内酯电纺丝支架的脱细胞生物活性
Q1 Materials Science Pub Date : 2016-01-14 DOI: 10.1515/bglass-2016-0011
William C. Lepry, Sophia Smith, L. Liverani, A. Boccaccini, S. Nazhat
Abstract Recently, sol-gel derived borate glasses (BGs) have shown unprecedented conversion rates to bone-like mineral (hydroxycarbonated apatite). In an effort to explore their potential applications in bone tissue engineering, this study reports on the fabrication and characterization of BG particle incorporated electrospun "- polycaprolactone (PCL) fibrous composites. The electrospinning technique successfully incorporated PCL fibres with BG particles at 2.5 and 5 w/v%, with the higher BG loading creating a three-dimensional cotton-wool like morphology. Dynamic vapour sorption showed greater extents of mass change with BG content attributable to water sorption, and indicating greater reactivity in the composite systems. In vitro bioactivity was investigated in simulated body fluid for up to 7 days. Scanning electron microscopy, Fourier-transform infrared spectroscopy and xray diffraction indicated apatite formation in the 5 w/v% incorporated composite scaffold, which initiated as early as day 3. In summary, sol-gel derived BGs incorporatedfibrous electrospun PCL composites indicate rapid reactivity and bioactivity with potential applications in mineralized tissue engineering.
最近,溶胶-凝胶衍生的硼酸盐玻璃(BGs)显示出前所未有的骨样矿物(羟基碳酸盐磷灰石)的转化率。为了探索其在骨组织工程中的潜在应用,本研究报道了BG颗粒掺杂“-聚己内酯”(PCL)纤维复合材料的制备和表征。静电纺丝技术成功地将含有BG颗粒的PCL纤维以2.5和5 w/v%的速度掺入,具有较高的BG负载,形成了类似于棉絮的三维形态。动态水蒸气吸附表现出更大程度的质量变化与BG含量归因于水的吸附,表明复合体系的反应性更强。在模拟体液中研究其体外生物活性长达7天。扫描电镜、傅里叶变换红外光谱和x射线衍射表明,掺入率为5 w/v%的复合支架中磷灰石的形成早在第3天就开始了。综上所述,溶胶凝胶衍生的BGs结合纤维静电纺PCL复合材料具有快速反应性和生物活性,在矿化组织工程中具有潜在的应用前景。
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引用次数: 23
Sodium-free mixed alkali bioactive glasses 无钠混合碱生物活性玻璃
Q1 Materials Science Pub Date : 2016-01-14 DOI: 10.1515/bglass-2016-0012
D. Brauer, R. Brückner, M. Tylkowski, L. Hupa
Abstract Two sodium-free mixed alkali series of bioactive glasses based on compositions Bioglass 45S5 and ICIE1, containing lithium and/or potassium as alkali ions, were prepared by a melt-quench route. Thermal properties showed the well-known mixed alkali effect, with glass transition and crystallisation temperatures and the coefficient of thermal expansion going either through a minimum or a maximum for the mixed alkali composition, resulting in a wider processing window. Ion release, by contrast, was controlled by the modifier ionic radius, with ion release rates in dynamic and static dissolution studies increasing for potassium-substituted glasses compared to the composition containing lithium as the only alkali ion. This was caused by pronounced changes in oxygen packing density and molar volume of the glasses owing to the differences in ionic radii (76 pm for Li+ and 138 pm for K+). Partially substituting one alkali for another therefore helps to improve high temperature processing of bioactive glasses and can also be used to control or tailor ion release.
摘要:以Bioglass 45S5和ICIE1为原料,以锂和/或钾为碱离子,采用熔淬法制备了两种无钠混合碱系列生物活性玻璃。热性能表现出众所周知的混合碱效应,对于混合碱成分,玻璃化转变和结晶温度以及热膨胀系数要么最小要么最大,从而导致更宽的加工窗口。相比之下,离子释放受离子半径调节剂的控制,在动态和静态溶解研究中,与含锂作为唯一碱离子的组合物相比,钾取代玻璃的离子释放率增加。这是由于离子半径(Li+为76 pm, K+为138 pm)的差异导致玻璃的氧堆积密度和摩尔体积的显著变化造成的。因此,用一种碱代替另一种碱有助于改善生物活性玻璃的高温处理,也可用于控制或调整离子释放。
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引用次数: 17
Monodispersed strontium containing bioactive glass nanoparticles and MC3T3-E1 cellular response 单分散含锶生物活性玻璃纳米颗粒与MC3T3-E1细胞反应
Q1 Materials Science Pub Date : 2016-01-05 DOI: 10.1515/bglass-2016-0009
Parichart Naruphontjirakul, Sarah L. Greasley, Shu Chen, A. Porter, Julian R. Jones
Abstract Non-porous monodispersed strontium containing bioactive glass (Si2O-CaO-SrO) nanoparticles (Sr- BGNPs), were synthesised using a modified Stöber process. Silica nanoparticles (Si-NPs) with diameters 90 ± 10 nm were produced through hydrolysis and polycondensation reactions of the silicon alkoxide precursor, tetraethyl orthosilicate (TEOS), prior to the incorporation of cations; calcium (Ca) and strontium (Sr), into the silica networks through heat treatment (calcination). Sr was substituted for Ca on a mole basis from non- (0SrBGNPs) to fullsubstitution (100SrBGNPs) in order to increase the amount of network modifiers in the Si-NPs. The different ratios of Si: Ca; 1:1.3 and 1:8.0, presented various elemental compositions (i.e. 77–92 mol% of SiO2). The effect of Si: Ca/Sr ratio on particle size, morphology and dispersitywas evaluated, as well as the in vitro cell viability effect of Sr- BGNPs and their dissolution products on pre-osteoblast cell line, MC3T3-E1. Sr incorporation did not affect particle size or dispersity. For 1:1.3 ratio, SrBGNPs caused no toxic effects on the cells and dissolution products of 75- and 100- SrBGNPs showed great potential to promote MC3T3-E1 activity.
摘要:采用改进的Stöber工艺合成了无孔单分散含生物活性玻璃(si20 - cao - sro)纳米粒子(Sr- BGNPs)。在阳离子掺入之前,通过硅烷氧化物前驱体正硅酸四乙酯(TEOS)的水解缩聚反应制备了直径为90±10 nm的二氧化硅纳米颗粒(Si-NPs);钙(Ca)和锶(Sr),通过热处理(煅烧)进入二氧化硅网络。为了增加Si-NPs中网络改性剂的数量,以摩尔为单位将Ca从非(0SrBGNPs)取代为全取代(100SrBGNPs)。不同比例的Si: Ca;1:13 .3和1:8.0,呈现出不同的元素组成(即77 ~ 92 mol%的SiO2)。研究了Si: Ca/Sr配比对成骨前细胞株MC3T3-E1的颗粒大小、形态和分散性的影响,以及Sr- BGNPs及其溶出产物对成骨前细胞株MC3T3-E1体外细胞活力的影响。锶掺入不影响颗粒的大小和分散性。在1:1.3的比例下,SrBGNPs对细胞没有毒性作用,75-和100- SrBGNPs的溶出产物对MC3T3-E1活性有很大的促进作用。
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引用次数: 28
Surface functionalization of phosphate-based bioactive glasses with 3-aminopropyltriethoxysilane (APTS) 3-氨基丙基三乙氧基硅烷(APTS)表面功能化磷酸酯基生物活性玻璃
Q1 Materials Science Pub Date : 2016-01-05 DOI: 10.1515/bglass-2016-0007
J. Massera, A. Mishra, S. Guastella, S. Ferraris, E. Verné
Abstract The effect of SrO substitution for CaO, in the 50P2O5-10Na2O-(40-x)CaO-xSrO glass system, on the ability to graft 3-aminopropyltriethoxysilane (APTS) at the glass surface has been investigated and is partially compared to changes occurring further from the surface. The step used for the APTS grafting led to Na leaching and successively to Ca and/or Sr leaching. This gave rise to a P2O5- rich glass surface, especially on sample containing both Ca and Sr ions. The hydration of the phosphate chainswas found to be the most pronounced for the glasses containing large quantity of SrO as evidenced by contact angle and X-ray photoelectron spectroscopy (XPS). The increase in phosphate chain hydration was attributed to the expansion of the glass network when Sr ions are introduced. Finally, based on the N1s XPS peak, N species were found at the surface of the glasses in two configurations: NH2 and – NH2-OH as proof of APTS grafting. APTS grafting on phosphate glass is of importance for the grafting of proteins.
摘要研究了50P2O5-10Na2O-(40-x)CaO- xsro玻璃体系中SrO取代CaO对玻璃表面接枝3-氨基丙基三乙氧基硅烷(APTS)能力的影响,并将其与表面以外发生的变化进行了部分比较。APTS接枝的步骤导致Na浸出,然后是Ca和/或Sr浸出。这就产生了富含P2O5的玻璃表面,特别是在同时含有Ca和Sr离子的样品上。接触角和x射线光电子能谱(XPS)证明,磷酸盐链的水化作用在含有大量SrO的玻璃中最为明显。磷酸链水化的增加是由于锶离子的引入使玻璃网膨胀。最后,根据N1s的XPS峰,在玻璃表面发现了NH2和- NH2- oh两种构型的N种,证明了APTS接枝的存在。磷酸玻璃上的APTS接枝对于蛋白质的接枝具有重要意义。
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引用次数: 9
Structuring of bioactive glass surfaces at the micrometer scale by direct casting intended to influence cell response 通过直接铸造在微米尺度上构建生物活性玻璃表面,旨在影响细胞反应
Q1 Materials Science Pub Date : 2016-01-05 DOI: 10.1515/bglass-2016-0008
Barbara Pföss, M. Höner, Monika Wirth, A. Bührig-Polaczek, H. Fischer, R. Conradt
Abstract Defect-free bioactive glass surfaces with a grooved microstructure at the low micrometer scale were achieved by a mold casting process. The process was applied to the well-known glass compositions 45S5 and 13–93. Such microstructured surfaces may exhibit especially favorable conditions for bone cell orientation and growth. The aim of the study was to assess the parameter range for a successful casting process and thus to produce samples suitable to investigate the interaction between structured surfaces and relevant cells. Viscous flow in its temperature dependence and thermal analysis were analyzed to identify a suitable process window and to design a manageable time-temperature process scheme. Counteracting effects such as formation of chill ripples, mold sticking and build-up of permanent thermal stress in the glass had to be overcome. A platinum gold alloy was chosen as mold material with the mold surface bearing the mother shape of the microstructure to be imprinted on the glass surface. First experiments studying the behavior of osteoblast-like cells, seeded on these microstructured glass surfaces revealed excellent viability and an orientation of the cells along the microgrooves. The presented results show that direct casting is a suitable process to produce defined microstructures on bioactive glass surfaces.
摘要采用模具铸造工艺,在低微米尺度上获得了具有沟槽微结构的无缺陷生物活性玻璃表面。该工艺应用于著名的玻璃组合物45S5和13-93。这种微结构表面可能对骨细胞的定向和生长表现出特别有利的条件。该研究的目的是评估成功铸造工艺的参数范围,从而产生适合研究结构表面和相关细胞之间相互作用的样品。对粘性流动的温度依赖性和热分析进行了分析,确定了合适的过程窗口,设计了可管理的时间-温度过程方案。必须克服诸如冷波纹的形成、模具粘着和玻璃中永久热应力的积累等抵消效应。选用铂金合金作为模具材料,模具表面承载着待压印在玻璃表面的微观结构的母形。第一次实验研究了在这些微结构的玻璃表面上播种的成骨细胞样细胞的行为,结果显示了良好的活力和细胞沿着微槽的方向。结果表明,直接铸造是在生物活性玻璃表面产生明确微观结构的合适工艺。
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引用次数: 1
After bleaching enamel remineralization using a bioactive glass-ceramic (BioSilicate®) 用生物活性玻璃陶瓷(bio硅酸盐®)漂白牙釉质再矿化
Q1 Materials Science Pub Date : 2016-01-01 DOI: 10.1515/bglass-2016-0001
A. Rastelli, G. Nicolodelli, R. A. Romano, D. Milori, I. L. O. Perazzoli, E. J. Ferreira, A. Pedroso, M. T. Souza, O. Peitl, Edgar Dutra Zanotto
Abstract Tooth bleaching agents may weaken the tooth structure, therefore, it is important to minimize any risks of enamel and dentine damage caused by them. In this way, different materials have been used to avoid or minimize the tooth damage during bleaching. Recently, bioactive glasses have been demonstrated to be effective in mineralization of dental structures. Therefore, this study evaluated the effect of BioSilicate® (a polycrystalline bioactive glass-ceramic) after bleaching by Laser-induced breakdown spectroscopy (LIBS) technique. Bovine dental blocks with 4 × 4 × 3 mm were obtained (n = 20), sequentially embedded in epoxy resin and then polished. Bleaching was performed using 35% hydrogen peroxide (Whiteness HP). Calcium (Ca) and phosphate (P) intensity values by LIBSwere obtained before the treatment (T0, baseline – control Group), after bleaching (T1), and after BioSilicate® application (T2). The use of BioSilicate® after bleaching showed to be an optimal way to remineralize enamel surface making BioSilicate® application a promising adjunct step to avoid or minimize the mineral loss on enamel surface after bleaching.
牙齿漂白剂可能会削弱牙齿的结构,因此,尽量减少它们对牙釉质和牙本质的损害是很重要的。因此,不同的材料被用来避免或减少牙齿在漂白过程中的损伤。近年来,生物活性玻璃已被证明是有效的矿化牙齿结构。因此,本研究利用激光诱导击穿光谱(LIBS)技术评估了生物硅酸盐(一种多晶生物活性玻璃陶瓷)漂白后的效果。获得4 × 4 × 3 mm的牛牙块(n = 20),依次包埋在环氧树脂中,然后抛光。使用35%过氧化氢(白度HP)进行漂白。在处理前(T0,基线-对照组)、漂白后(T1)和应用BioSilicate®后(T2),通过libs4测定钙(Ca)和磷酸盐(P)强度值。漂白后使用生物硅酸盐®是牙釉质表面再矿化的最佳方法,使生物硅酸盐®应用成为避免或尽量减少漂白后牙釉质表面矿物损失的有希望的辅助步骤。
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引用次数: 11
Angiogenic Effect of Bioactive Borate Glass Microfibers and Beads in the Hairless Mouse 生物活性硼酸玻璃微纤维和微珠对无毛小鼠血管生成的影响
Q1 Materials Science Pub Date : 2015-12-24 DOI: 10.1515/bglass-2015-0017
R. J. Watters, Roger F. R. Brown, D. Day
Abstract The purpose of this project was to investigate the angiogenic mechanism of bioactive borate glass for soft tissue repair in a ‘hairless’ SKH1 mouse model. Subcutaneous microvascular responses to bioactive glass microfibers (45S5, 13-93B3, and 13-93B3Cu) and bioactive glass beads (13-93, 13-93B3, and 13-93B3Cu) were assessed via: noninvasive imaging of skin microvasculature; histomorphometry of microvascular densities; and quantitative PCR measurements of mRNA expression of VEGF and FGF-2 cytokines. Live imaging via dorsal skin windows showed the formation at twoweeks of a halo-like structure infused with microvessels surrounding implanted boratebased 13-93B3 and 13-93B3Cu glass beads, a response not observed with silicate-based 13-93 glass beads. Quantitative histomorphometry of tissues implanted with plugs of 45S5, 13-93B3, and 13-93B3Cu glass microfibers revealed microvascular densities that were 1.6-, 2.3-, and 2.7-times higher, respectively, than the sham control valueswhereas 13-93, 13-93B3, and 13-93B3Cu glass beads caused the microvascular density to increase 1.3-, 1.6-, and 2.5-fold, respectively, relative to sham controls. Quantitative PCR measurements indicate a marginally significant increased expression of VEGF mRNA in tissues with 13-93B3Cu glass beads, an outcome that supported the hypothesis that copper-doped borate glass could promote VEGF expression followed by angiogenesis for enhanced wound healing.
本项目旨在研究生物活性硼酸盐玻璃在“无毛”SKH1小鼠模型中用于软组织修复的血管生成机制。皮下微血管对生物活性玻璃微纤维(45S5、13-93B3和13-93B3Cu)和生物活性玻璃微珠(13-93、13-93B3和13-93B3Cu)的反应通过以下方式评估:皮肤微血管无创成像;微血管密度组织形态学;定量PCR检测VEGF和FGF-2细胞因子mRNA表达。通过背部皮肤窗口的实时成像显示,两周后,植入的硼酸盐基13-93B3和13-93B3Cu玻璃珠周围形成了一个充满微血管的晕状结构,而硅酸盐基13-93玻璃珠则没有观察到这种反应。对植入45S5、13-93B3和13-93B3Cu玻璃微纤维的组织进行定量组织形态学分析,结果显示,微血管密度分别比假手术对照组高1.6倍、2.3倍和2.7倍,而13-93、13-93B3和13-93B3Cu玻璃微珠的组织微血管密度分别比假手术对照组高1.3倍、1.6倍和2.5倍。定量PCR检测结果显示,在13-93B3Cu玻璃微珠的组织中,VEGF mRNA的表达略有显著增加,这一结果支持了铜掺杂硼酸盐玻璃可以促进VEGF表达和血管生成,从而促进伤口愈合的假设。
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引用次数: 6
Dissolution behavior and cell compatibility of alkali-free MgO-CaO-SrO-TiO2-P2O5 glasses for biomedical applications 生物医学用无碱MgO-CaO-SrO-TiO2-P2O5玻璃的溶解行为和细胞相容性
Q1 Materials Science Pub Date : 2015-12-18 DOI: 10.1515/bglass-2015-0015
Sungho Lee, A. Obata, D. Brauer, T. Kasuga
Abstract Owing to their controlled solubility, phosphate invert glasses are of interest for use as temporary implant materials or tissue engineering scaffolds for controlled ion release.MgO-CaO-SrO-TiO2-P2O5 invert glasses were prepared and their dissolution behavior and cell response were examined.MgO addition to the phosphate invert glass system improved glass formation, owing to the relatively large field strength of Mg2+ ions. In osteoblastlike MC3T3-E1 cell culture tests, cell numbers on the invert glasses were significantly larger compared with the control, possibly caused by the release of Mg2+ ions promoting enhanced cell adhesion and proliferation. Alkaline phosphatase (ALP) activity varied with glass composition, with higher strontium for calcium substitution (33 to 100%) showing highest ALP activity. This effect may be caused by the release of strontium ions from the glasses.
由于其可控制的溶解度,磷酸盐倒置玻璃被用作控制离子释放的临时植入材料或组织工程支架。制备了MgO-CaO-SrO-TiO2-P2O5倒置玻璃,并对其溶解行为和细胞反应进行了研究。由于Mg2+离子相对较大的场强,在磷酸盐转化玻璃体系中加入MgO可以改善玻璃的形成。在MC3T3-E1类成骨细胞培养试验中,倒置玻璃上的细胞数量明显大于对照,这可能是由于Mg2+离子的释放促进了细胞的粘附和增殖。碱性磷酸酶(ALP)活性随玻璃成分的不同而变化,高钙取代锶(33 ~ 100%)显示出最高的ALP活性。这种效应可能是由锶离子从玻璃中释放出来引起的。
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引用次数: 9
Preparation of hollow bioactive glass nanofibers by a facile electrospinning method 静电纺丝法制备中空生物活性玻璃纳米纤维
Q1 Materials Science Pub Date : 2015-11-03 DOI: 10.1515/bglass-2015-0013
Botao Song, Liang Wu, Chengtie Wu, Jiang Chang
Abstract In this communication, hollow bioactive glass (BG) nanofibers were fabricated via a single-nozzle electrospinning method. The morphology of the prepared hollow BG nanofibers was observed by SEM and TEM, and the results showed that BG nanofibers had a continuous hollow interior. The hollow BG nanofibers were incubated in simulated body fluid (SBF) to investigate their apatitemineralization ability, and the result showed that after incubation for 6 h a flower-like apatite was observed on the surface of hollowBGnanofibers, and the Fourier transform infrared (FTIR) result further confirmed the formation of apatite. The results suggested that hollow BG nanofibers could be used for drug delivery and bone regeneration applications due to their unique hollow structure and bioactivity.
本文采用单喷嘴静电纺丝法制备了中空生物活性玻璃(BG)纳米纤维。通过SEM和TEM对制备的空心BG纳米纤维的形貌进行了观察,结果表明BG纳米纤维具有连续中空的内部结构。将中空BG纳米纤维置于模拟体液(SBF)中孵育,考察其磷灰石矿化能力,结果表明,孵育6 h后,中空BG纳米纤维表面出现花状磷灰石,傅里叶变换红外(FTIR)结果进一步证实了磷灰石的形成。结果表明,由于其独特的中空结构和生物活性,空心BG纳米纤维可用于药物输送和骨再生。
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引用次数: 10
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Biomedical Glasses
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