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Bioactive magnetic glass-ceramics for cancer treatment 用于癌症治疗的生物活性磁性玻璃陶瓷
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0013
M. Velasco, M. T. Souza, M. Crovace, A. J. Aparecido de Oliveira, Edgar Dutra Zanotto
Abstract After five decades of research on bioactive glasses and glass-ceramics, these materials became of considerable interest due to their revolutionary potential for numerous health applications, including cancer treatment. One advantage of glass-ceramics compared with other materials – such as metallic alloys and polymers – is their capability of being highly bioactive and, if desired, containing magnetic phases. Hyperthermia (HT) is an alternative for treating cancer; the strategy is to increase the temperature of the tumor using an external magnetic field that increases the temperature of an implanted magnetic material, which works as an internal heat source. This local increase of temperature, ideally to ~43°C, could kill cancer cells in situ without damaging the healthy surrounding tissue. To achieve such goal, a material that presents a balance between proper magnetic properties and bioactivity is necessary for the safe applicability and successful performance of the HT treatment. Certainly, achieving this ideal balance is the main challenge. In this article we review the state-of-the-art on glass-ceramics intended for HT, and explore the current difficulties in their use for cancer treatment, starting with basic concepts and moving onto recent developments and challenges.
摘要经过50年对生物活性玻璃和微晶玻璃的研究,这些材料因其在许多健康应用(包括癌症治疗)中的革命性潜力而引起了人们的极大兴趣。与金属合金和聚合物等其他材料相比,玻璃陶瓷的一个优点是具有高度的生物活性,如果需要,还可以包含磁相。热疗(HT)是治疗癌症的一种替代方法;该策略是使用外部磁场来提高肿瘤的温度,该磁场可以提高植入的磁性材料的温度,这种材料起到内部热源的作用。这种局部温度升高,理想情况下为43°C,可以原位杀死癌症细胞,而不会损害健康的周围组织。为了实现这一目标,在适当的磁性和生物活性之间保持平衡的材料对于HT处理的安全适用性和成功性能是必要的。当然,实现这种理想的平衡是主要的挑战。在这篇文章中,我们回顾了用于HT的玻璃陶瓷的最新技术,并探讨了目前在癌症治疗中使用玻璃陶瓷的困难,从基本概念开始,转向最新的发展和挑战。
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引用次数: 23
Bioactivity and dissolution behavior of boron-containing bioactive glasses under static and dynamic conditions in different media 含硼生物活性玻璃在静态和动态条件下在不同介质中的生物活性和溶解行为
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0011
M. Arango-Ospina, L. Hupa, A. Boccaccini
Abstract The present study reports the dissolution studies of a family of boron-doped bioactive glasses based on the composition ICIE16. Simulated body fluid (SBF), Tris-buffered solution and lactic acid were used as dissolution media for studies under static and dynamic conditions. The leaching of ions from the glasses under the evaluated conditions and media was compared and the bioactive behaviour of the glasses was evaluated. Influence of the incorporation of boron in the thermal properties of the glass was also analysed. Glasses exhibited faster bioactivity under dynamic dissolution configuration compared to static conditions. Moreover, the glass dissolution rate was faster in acidic conditions than in SBF or Tris solutions. It was found that at increasing boron content the dissolution of the glass is faster.
摘要本研究报道了一类基于组合物ICIE16的硼掺杂生物活性玻璃的溶解研究。在静态和动态条件下,使用模拟体液(SBF)、Tris缓冲溶液和乳酸作为溶解介质进行研究。比较了在所评估的条件和介质下从玻璃中浸出离子的情况,并评估了玻璃的生物活性行为。还分析了硼的掺入对玻璃热性能的影响。与静态条件相比,玻璃在动态溶解配置下表现出更快的生物活性。此外,玻璃在酸性条件下的溶解速率比在SBF或Tris溶液中更快。研究发现,随着硼含量的增加,玻璃的溶解速度更快。
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引用次数: 33
Bioglass at 50 – A look at Larry Hench’s legacy and bioactive materials 50岁的生物玻璃——Larry Hench的遗产和生物活性材料
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0014
D. Greenspan
Abstract In 1969, fifty years ago, a young professor of ceramic engineering created a 4-component glass to be used as a bone replacement material. That material became known as “Bioglass” and more generally as a class of materials known as bioactive glass. Those first experiments conducted by Dr. Larry Hench completely shifted the paradigm of how the biomaterials and medical communities look at the interactions between inorganic materials and tissues in the body. This article will touch on just a few highlights of the development of bioactive glasses and relate those to the concepts of bioactivity and tissue bonding.
摘要在50年前的1969年,一位年轻的陶瓷工程教授创造了一种四组分玻璃,用作骨替代材料。这种材料后来被称为“生物玻璃”,更广泛地说是一类被称为生物活性玻璃的材料。拉里·亨奇博士进行的第一批实验彻底改变了生物材料和医学界如何看待无机材料和体内组织之间的相互作用的范式。这篇文章将只涉及生物活性玻璃发展的几个亮点,并将其与生物活性和组织结合的概念联系起来。
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引用次数: 12
Mechanical characterization of pore-graded bioactive glass scaffolds produced by robocasting 机器人浇铸制备的孔分级生物活性玻璃支架的力学性能
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0012
J. Barberi, A. Nommeots-Nomm, E. Fiume, E. Verné, J. Massera, F. Baino
Abstract Since the discovery of 45S5 Bioglass® by Larry Hench, bioactive glasses have been widely studied as bone substitute materials and, in more recent years, have also shown great promise for producing three-dimensional scaffolds. The development of additive manufacturing techniques and their application in bone tissue engineering allows the design and fabrication of complex structures with controlled porosity. However, achieving strong and mechanically-reliable bioactive glass scaffolds is still a great challenge. Furthermore, there is a relative paucity of studies reporting an exhaustive assessment of other mechanical properties than compressive strength of glass-derived scaffolds. This research work aimed at determining key mechanical properties of silicate SiO2-Na2O-K2OMgO-CaO-P2O5 glass scaffolds fabricated by robocasting and exhibiting a porosity gradient. When tested in compression, these scaffolds had a strength of 6 MPa, a Young’s modulus around 340 MPa, a fracture energy of 93 kJ/m3 and a Weibull modulus of 3, which provides a quantification of the scaffold reliability and reproducibility. Robocasting was a suitable manufacturing method to obtain structures with favorable porosity and mechanical properties comparable to those of the human cancellous bone, which is fundamental regarding osteointegration of bone implants.
摘要自从Larry Hench发现45S5 Bioglass®以来,生物活性玻璃作为骨替代材料得到了广泛的研究,近年来,在生产三维支架方面也显示出了巨大的前景。增材制造技术的发展及其在骨组织工程中的应用允许设计和制造具有可控孔隙率的复杂结构。然而,实现坚固且机械可靠的生物活性玻璃支架仍然是一个巨大的挑战。此外,报告对玻璃衍生支架抗压强度以外的其他机械性能进行详尽评估的研究相对较少。本研究工作旨在确定通过自动铸造制造并呈现孔隙率梯度的硅酸盐SiO2-Na2O-K2OMgO-CaO-P2O5玻璃支架的关键力学性能。当在压缩中测试时,这些支架具有6MPa的强度、约340MPa的杨氏模量、93kJ/m3的断裂能和3的威布尔模量,这提供了支架可靠性和再现性的量化。机器人定位是一种合适的制造方法,可以获得具有与人类松质骨相当的良好孔隙率和机械性能的结构,这是骨植入物骨整合的基础。
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引用次数: 17
Synthesis and physico-chemical characterization of fluoride (F)- and silver (Ag)-substituted sol-gel mesoporous bioactive glasses 氟和银取代的溶胶-凝胶介孔生物活性玻璃的合成及理化性质
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0015
S. Kargozar, F. Baino, S. Banijamali, M. Mozafari
Abstract Synthesis and use of novel compositions of bioactive glasses (BGs) for hard tissue engineering are of important significance in the biomedical field. In this study, we successfully synthesized a series of 58S-based BGs containing fluoride (F−) and silver (Ag+) ions through a sol-gel method for possible use in bone/dental regeneration and antibacterial strategies. Characterizations of samples were performed by using thermal analyses (thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC)), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), textural analysis (N2 adsorption-desorption), and morphological observations by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The obtained data revealed that the fabricated BGs are in a glassy state before incubation in the Kokubo’s simulated body fluid (SBF), and an apatite-like layer is formed on their surface after 7 days of immersion in SBF. The size of the glass particles was in the nano-range (about 100 nm or below), and their pore size was in the mesoporous range (15-25 nm). These early results suggest that the F- and Ag-doped glasses show promise as multifunctional bioactive materials for bone/dental tissue engineering.
摘要用于硬组织工程的新型生物活性玻璃的合成和应用在生物医学领域具有重要意义。在本研究中,我们通过溶胶凝胶法成功合成了一系列含有氟(F-)和银(Ag+)离子的58S基BGs,用于骨/牙再生和抗菌策略。通过使用热分析(热重分析(TGA)和差示扫描量热法(DSC))、X射线衍射(XRD)、傅立叶变换红外光谱(FTIR)、结构分析(N2吸附-解吸)以及通过透射电子显微镜(TEM)和扫描电子显微镜(SEM)的形态观察来对样品进行表征。所获得的数据显示,在Kokubo模拟体液(SBF)中孵育之前,所制备的BGs处于玻璃态,并且在SBF中浸泡7天后,在其表面形成磷灰石样层。玻璃颗粒的尺寸在纳米范围内(约100nm或以下),并且它们的孔径在介孔范围内(15-25nm)。这些早期结果表明,F和Ag掺杂玻璃有望成为骨/牙组织工程的多功能生物活性材料。
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引用次数: 16
Effect of dissolution rate and subsequent ion release on cytocompatibility properties of borophosphate glasses 溶解速率和随后的离子释放对硼磷酸盐玻璃细胞相容性的影响
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0008
N. Sharmin, M. S. Hasan, M. Islam, C. Pang, Fu Gu, A. Parsons, I. Ahmed
Abstract Present work explores the relationship between the composition, dissolution rate, ion release and cytocompatibility of a series of borophosphate glasses. While, the base glass was selected to be 40mol%P2O5-16mol%CaO-24mol%MgO-20mol%Na2O, three B2O3 modified glass compositions were formulated by replacing Na2O with 1, 5 and 10 mol% B2O3. Ion release study was conducted using inductively coupled plasma atomic emission spectroscopy (ICP-AES). The thermal scans of the glasses as determined by differential scanning calorimetry (DSC) revealed an increment in the thermal properties with increasing B2O3 content in the glasses. On the other hand, the dissolution rate of the glasses decreased with increasing B2O3 content. To identify the effect of boron ion release on the cytocompatibility properties of the glasses, MG63 cells were cultured on the surface of the glass discs. The in vitro cell culture study suggested that glasses with 5 mol% B2O3 (P40B5) showed better cell proliferation and metabolic activity as compares to the glasses with 10 mol% (P40B10) or with no B2O3 (P40B0). The confocal laser scanning microscopy (CLSM) images of live/dead stained MG63 cells attached to the surface of the glasses also revealed that the number of dead cells attached to P40B5 glasses were significantly lower than both P40B0 and P40B10 glasses.
摘要本文研究了一系列硼磷酸盐玻璃的组成、溶解速率、离子释放与细胞相容性之间的关系。选择40mol%P2O5-16mol%CaO-24mol%MgO-20mol%Na2O为基料玻璃,用1、5、10 mol% B2O3代替Na2O,配制出3种B2O3改性玻璃。利用电感耦合等离子体原子发射光谱(ICP-AES)研究离子释放。差示扫描量热法(DSC)对玻璃的热扫描结果表明,随着B2O3含量的增加,玻璃的热性能有所增加。另一方面,随着B2O3含量的增加,玻璃的溶解速率降低。为了确定硼离子释放对玻璃细胞相容性的影响,我们在玻璃盘表面培养MG63细胞。体外细胞培养研究表明,添加5 mol% B2O3 (P40B5)的玻璃比添加10 mol% (P40B10)或不添加B2O3 (P40B0)的玻璃具有更好的细胞增殖和代谢活性。通过共聚焦激光扫描显微镜(CLSM)对附着在P40B5和P40B10玻璃表面的MG63细胞进行观察,发现附着在P40B5玻璃表面的MG63细胞死亡数量明显低于P40B0和P40B10玻璃表面。
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引用次数: 7
Dissolution and bioactivity of a sol-gel derived borate glass in six different solution media 溶胶-凝胶衍生硼酸盐玻璃在六种不同溶液介质中的溶解性和生物活性
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0009
William C. Lepry, E. Rezabeigi, Sophia Smith, S. Nazhat
Abstract Sol-gel derived bioactive borate glasses (SGBGs) rapidly convert to hydroxycarbonated apatite (HCA) in simulated body fluid (SBF), in vitro. While previous studies have examined the influence of processing and composition on bioactivity, the effect of the in vitro dissolution media has not been well examined for these glasses. In this study, the mineral conversion of a SGBG substituted 45S5 Bioglass® formulation (“B46”, (46.1)B2O3-(26.9)CaO-(24.4)Na2O-(2.6)P2O5, mol%), was examined in six different dissolution media: SBF, tris(hydroxymethyl)aminomethane (TRIS, pH 7.4) buffer, Dulbecco’s phosphate buffered saline (PBS, 1X), Dulbecco’s Modified Eagle Medium (DMEM, 1X), 0.9% Saline (SAL), and deionized water (DIW) at 1.5 mg/mL for 10 min, 2h, and 1d. All media underwent a rapid increase in pH as a result of glass dissolution and ion release. B46 in SBF, TRIS, and PBS converted to HCA while B46 in DMEM, SAL, and DIW converted to calcite according to attenuated total reflectance-Fourier-transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. The ratio of B46 to SBF was also examined at 3, 6, 12, and 24 mg/mL for 1d. These results help elucidate the dissolution and mineral conversion of borate glasses and help provide insights into optimizing pre-conditioning treatments for both in vitro and in vivo analyses.
摘要溶胶-凝胶衍生的生物活性硼酸盐玻璃(SGBG)在体外模拟体液(SBF)中快速转化为羟基碳酸磷灰石(HCA)。虽然先前的研究已经检验了加工和组成对生物活性的影响,但体外溶解介质对这些玻璃的影响还没有得到很好的检验。在本研究中,SGBG取代的45S5 Bioglass®制剂(“B46”,(46.1)B2O3-(26.9)CaO-(24.4)Na2O-(2.6)P2O5,mol%)的矿物转化率在六种不同的溶解介质中进行了检测:SBF、三(羟甲基)氨基甲烷(tris,pH 7.4)缓冲液、Dulbecco磷酸盐缓冲盐水(PBS,1X)、Dulbecko改良鹰培养基(DMEM,1X)和0.9%盐水(SAL),和1.5mg/mL的去离子水(DIW),持续10分钟、2小时和1天。由于玻璃溶解和离子释放,所有介质的pH值都迅速增加。根据衰减全反射傅立叶变换红外光谱、X射线衍射和扫描电子显微镜,SBF、TRIS和PBS中的B46转化为HCA,而DMEM、SAL和DIW中的B46。B46与SBF的比例也在3、6、12和24mg/mL下检测1d。这些结果有助于阐明硼酸盐玻璃的溶解和矿物转化,并有助于为优化体外和体内分析的预处理提供见解。
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引用次数: 11
Insight into the atomic scale structure of CaF2-CaO-SiO2 glasses using a combination of neutron diffraction, 29Si solid state NMR, high energy X-ray diffraction, FTIR, and XPS 利用中子衍射、29Si固体核磁共振、高能x射线衍射、FTIR和XPS等手段对CaF2-CaO-SiO2玻璃的原子尺度结构进行了深入研究
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0010
L. F. Chungong, M. Isaacs, A. Morrell, Laura A Swansbury, A. Hannon, A. Lee, G. Mountjoy, Richard A. Martin
Abstract Bioactive glasses are important for biomedical and dental applications. The controlled release of key ions, which elicit favourable biological responses, is known to be the first key step in the bioactivity of these materials. Properties such as bioactivity and solubility can be tailored for specific applications. The addition of fluoride ions is particularly interesting for dental applications as it promotes the formation of fluoro-apatite. To date there have been mixed reports in the literature on how fluorine is structurally incorporated into bioactive glasses. To optimize the design and subsequent bioactivity of these glasses, it is important to understand the connections between the glass composition, structure and relevant macroscopic properties such as apatite formation and glass degradation in aqueous media. Using neutron diffraction, high energy X-ray diffraction, 29Si NMR, FTIR and XPS we have investigated the atomic scale structure of mixed calcium oxide / calcium fluoride silicate based bioactive glasses. No evidence of direct Si-F bonding was observed, instead fluorine was found to bond directly to calcium resulting in mixed oxygen/fluoride polyhedra. It was therefore concluded that the addition of fluorine does not depolymerise the silicate network and that the widely used network connectivity models are valid in these oxyfluoride systems.
摘要生物活性玻璃在生物医学和牙科应用中具有重要意义。众所周知,关键离子的控制释放是这些材料生物活性的第一个关键步骤,它会引发有利的生物反应。生物活性和溶解度等特性可以针对特定应用进行定制。氟离子的添加对于牙科应用尤其令人感兴趣,因为它促进了氟磷灰石的形成。到目前为止,关于氟如何在结构上被掺入生物活性玻璃的文献报道不一。为了优化这些玻璃的设计和随后的生物活性,重要的是了解玻璃的组成、结构和相关宏观性质之间的联系,如磷灰石的形成和玻璃在水介质中的降解。利用中子衍射、高能X射线衍射、29SiNMR、FTIR和XPS研究了混合氧化钙/氟化钙-硅酸盐基生物活性玻璃的原子尺度结构。没有观察到Si-F直接键合的证据,相反,发现氟直接键合到钙上,产生混合的氧/氟多面体。因此得出结论,氟的添加不会使硅酸盐网络解聚,并且广泛使用的网络连接模型在这些含氟氧体系中是有效的。
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引用次数: 4
Special Issue: 50 Years of Bioactive Glasses: celebratory special issue in “Biomedical Glasses” 特辑:生物活性眼镜50周年纪念特辑《生物医学眼镜》
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0017
Julian R. Jones, F. Baino, A. Boccaccini
Even if the first paper of Prof. Larry Hench that introduced bioactive glass and its properties was published in 1971 (the seminal paper in J. Biomed. Mater. Res. [1]), the actual discovery of bioactive glass and its bone bonding properties dates back to 1969, in the laboratory of Prof. Hench at University of Florida, USA. Over the last 50 years, bioactive glasses, originally intended for applications as bone substitutingmaterials and small orthopedic implants, have expanded in their functionalities and applications, based on innovative chemical compositions and novel processing techniques, to areas such as biomedical coatings, dental care, scaffolds for tissue engineering, and as components of advanced devices for drug delivery, wound healing, soft tissue repair and potential uses in cancer treatment. The present special issue in "Biomedical Glasses" marks the 50th Anniversary of bioactive glass, including a collection of papers written by members of the bioactive glass research community, on a great variety of topics related to the development, properties and applications of bioactive glasses. The collection includes a review paper by David Greenspan, who was the main driving force behind the commercialization of Bioglass (the original bioactive glass composition) and subsequent products that evolved from it, from bone grafts to toothpaste. David summarizes the early development of bioactive glasses and highlights the legacy of Prof. Hench in the broad biomaterials field [2]. Another review paper, by the group of Edgar Zanotto, covers the emerging field of bioactive magnetic glass-ceramics for cancer treatment [3]. Application of bioactive glasses in bone cements is discussed in the papers of Wetzel et al. [4] andMokhtari et al. [5], while applications of different bioactive glasses in bone tissue engineering scaffolds are covered by the papers of Brokmann et al. [6], and Barberi et al. [7] and the field of wound healing and antibacterial effects of bioactive glasses is the subject of the paper of Jung et al. [8]. The special volume includes also several papers featuring the growing field of bioactive glasses incorporating biologically active ions, in this case: Cu [5], Mg [9], Zn [10], B [8, 11–13], F [14–16], Ag [15], Gd [17]. These studies cover fundamental investigations on the structure, crystallization behavior, thermal properties, biocompatibility, bioactivity, dissolution kinetics and biodegradability of a series of bioactive glasses of silicate, phosphate and borate composition, obtained by melting or sol-gel methods. We hope that the present volume will represent a valuable source of information for bioactive glass researchers and that it will be seen as a fitting collection to commemorate the 50th Anniversary of bioactive glass and the legacy of Prof. Larry Hench.
即使Larry Hench教授在1971年发表了第一篇介绍生物活性玻璃及其特性的论文(《J. Biomed》上的开创性论文)。板牙。Res. b[1]),生物活性玻璃及其骨粘合性能的实际发现可以追溯到1969年,在美国佛罗里达大学Hench教授的实验室。在过去的50年里,生物活性玻璃最初用于骨替代材料和小型骨科植入物,基于创新的化学成分和新的加工技术,其功能和应用范围已经扩展到生物医学涂层、牙科保健、组织工程支架等领域,以及作为药物输送、伤口愈合、软组织修复和癌症治疗等先进设备的组成部分。本期《生物医学眼镜》特刊纪念生物活性玻璃问世50周年,收录了由生物活性玻璃研究团体成员撰写的一系列论文,内容涉及生物活性玻璃的发展、特性和应用等诸多主题。该系列包括大卫·格林斯潘(David Greenspan)的一篇评论论文,他是生物玻璃(最初的生物活性玻璃成分)商业化的主要推动者,并由此衍生出从骨移植物到牙膏等后续产品。David总结了生物活性玻璃的早期发展,并强调了Hench教授在广泛的生物材料领域的遗产。另一篇由Edgar Zanotto小组撰写的综述文章,涵盖了用于癌症治疗的生物活性磁性微晶玻璃这一新兴领域。Wetzel et al.[4]和mokhtari et al.[5]的论文讨论了生物活性玻璃在骨水泥中的应用,而Brokmann et al.[6]和Barberi et al.[7]的论文涵盖了不同生物活性玻璃在骨组织工程支架中的应用,生物活性玻璃的伤口愈合和抗菌作用领域是Jung et al.[8]的论文的主题。该特刊还包括几篇介绍生物活性玻璃领域的论文,这些生物活性玻璃含有生物活性离子,在这种情况下:Cu [5], Mg [9], Zn [10], B [8,11 - 13], F [14-16], Ag [15], Gd[17]。这些研究涵盖了对硅酸盐、磷酸盐和硼酸盐组成的一系列生物活性玻璃的结构、结晶行为、热性能、生物相容性、生物活性、溶解动力学和生物降解性的基础研究,这些玻璃是通过熔融或溶胶-凝胶方法获得的。我们希望本卷将为生物活性玻璃研究人员提供有价值的信息来源,并将被视为纪念生物活性玻璃50周年和拉里·亨奇教授遗产的合适收藏。
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引用次数: 1
Crystallization behavior of SiO2–P2O5–CaO–MgO–Na2O–K2O bioactive glass powder SiO2–P2O5–CaO–MgO–Na2O–K2O生物活性玻璃粉末的结晶行为
Q1 Materials Science Pub Date : 2019-01-01 DOI: 10.1515/bglass-2019-0004
E. Fiume, E. Verné, F. Baino
Abstract The crystallization process of a bioactive silicate glass with 47.5SiO2-10Na2O-10K2O-10MgO-20CaO-2.5P2O5 molar composition was investigated by using nonisothermal differential t hermal a nalysis (DTA). T he DTA plots recorded at different heating rates exhibited a single crystallization peak. The activation energy for crystallization was estimated by applying the equations proposed by Kissinger and Matusita-Sakka. The Johnson-Mehl-Avrami exponent (n) was assessed by using the Ozawa and Augis-Bennett methods. The analyses suggest that a surface crystallization mechanism with one-dimensional crystal growth is predominant. The activation energy for viscous flow was also assessed (176 kJ/mol) and was found lower than the activation energy for crystallization (271 kJ/mol). This confirms the stability of 47.5B against crystallization and its good sinterability, which is a highly attractive feature for producing glass products of biomedical interest, such as bioactive porous scaffolds for bone repair.
摘要采用非等温差热分析(DTA)研究了47.5SiO2-10Na2O-10K2O-10MgO-20CaO-2.5P2O5摩尔比组成的生物活性硅酸盐玻璃的结晶过程。在不同加热速率下记录的DTA图显示出单一结晶峰。应用Kissinger和Matusita Sakka提出的方程估算了结晶的活化能。Johnson—Mehl—Avrami指数(n)采用Ozawa和Augis—Bennett方法进行评估。分析表明,一维晶体生长的表面结晶机制占主导地位。还评估了粘性流的活化能(176kJ/mol),发现其低于结晶的活化能。这证实了47.5B对结晶的稳定性及其良好的可烧结性,这对于生产生物医学感兴趣的玻璃产品(如用于骨修复的生物活性多孔支架)是非常有吸引力的特征。
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引用次数: 16
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Biomedical Glasses
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