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Bioactivity and Cell Compatibility of β-Wollastonite Derived from Rice Husk Ash and Limestone

机译:稻壳灰和石灰石衍生的β-硅灰石的生物活性和细胞相容性

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The aim of this study was to prepare β-wollastonite using a green synthesis method (autoclaving technique) without organic solvents and to study its bioactivity. To prepare β-wollastonite, the precursor ratio of CaO:SiO2 was set at 55:45. This mixture was autoclaved for 8 h and later sintered at 950 °C for 2 h. The chemical composition of the precursors was studied using X-ray fluorescence (XRF), in which rice husk ash consists of 89.5 wt % of SiO2 in a cristobalite phase and calcined limestone contains 97.2 wt % of CaO. The X-ray diffraction (XRD) patterns after sintering showed that only β-wollastonite was detected as the single phase. To study its bioactivity and degradation properties, β-wollastonite samples were immersed in simulated body fluid (SBF) for various periods of time. Throughout the soaking period, the molar ratio of Ca/P obtained was in the range of 1.19 to 2.24, and the phase detected was amorphous calcium phosphate, which was confirmed by scanning electron microscope with energy dispersive X-ray analysis (SEM/EDX) and XRD. Fourier-transform infrared spectroscopy (FTIR) analysis indicated that the peaks of the calcium and phosphate ions increased when an amorphous calcium phosphate layer was formed on the surface of the β-wollastonite sample. A cell viability and proliferation assay test was performed on the rice husk ash, calcined limestone, and β-wollastonite samples by scanning electron microscope. For heavy metal element evaluation, a metal panel that included As, Cd, Pb, and Hg was selected, and both precursor and β-wollastonite fulfilled the requirement of an American Society for Testing and Materials (ASTM F1538-03) standard specification. Apart from that, a degradation test showed that the loss of mass increased incrementally as a function of soaking period. These results showed that the β-wollastonite materials produced from rice husk ash and limestone possessed good bioactivity, offering potential for biomedical applications.
机译:这项研究的目的是使用绿色合成方法(高压灭菌技术)在没有有机溶剂的情况下制备β-硅灰石,并研究其生物活性。为了制备β-硅灰石,将CaO∶SiO 2的前体比率设定为55∶45。将该混合物高压灭菌8小时,然后在950℃下烧结2小时。使用X射线荧光(XRF)研究了前体的化学组成,其中稻壳灰分在方石英相中包含89.5 wt%的SiO2,煅烧石灰石包含97.2 wt%的CaO。烧结后的X射线衍射(XRD)图谱表明仅检测到β-硅灰石为单相。为了研究其生物活性和降解性能,将β-硅灰石样品浸入模拟体液(SBF)中不同时间。在整个浸泡过程中,所获得的Ca / P摩尔比在1.19至2.24的范围内,并且检测到的相为无定形磷酸钙,这通过扫描电子显微镜通过能量色散X射线分析(SEM / EDX)得以确认。和XRD。傅里叶变换红外光谱(FTIR)分析表明,当在β-硅灰石样品表面形成无定形磷酸钙层时,钙和磷酸根离子的峰增加。通过扫描电子显微镜对稻壳灰,煅烧石灰石和β-硅灰石样品进行了细胞活力和增殖测定测试。为了评估重金属元素,选择了包含As,Cd,Pb和Hg的金属板,并且前驱体和β-硅灰石均满足美国材料试验学会(ASTM F1538-03)标准规范的要求。除此之外,降解测试表明质量损失随浸泡时间的增加而逐渐增加。这些结果表明,由稻壳灰和石灰石生产的β-硅灰石材料具有良好的生物活性,为生物医学应用提供了潜力。

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