水热辅助常规溶胶-凝胶法合成生物活性玻璃70s30cmo

T. A. Tuan, E. Guseva, N. A. Tien, H. T. Anh, B. X. Vuong, L. Phuc, N. Q. Hien, B. T. Hoa, Nguyen Viet Long
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引用次数: 1

摘要

生物活性玻璃(bioglass)广泛采用传统的溶胶-凝胶法合成,包括两个主要步骤:溶胶和凝胶的形成。然而,从溶胶到凝胶的转化需要很长时间(5-7天)。本研究采用水热体系快速合成生物活性玻璃,缩短了溶胶到凝胶的转化时间。采用水热辅助常规溶胶-凝胶法合成了生物活性玻璃70SiO2-30CaO (mol%)(记为70S30C)。采用物理化学方法对合成玻璃进行了研究。体外模拟体液实验也对合成材料的生物活性进行了评价。结果表明,采用水热辅助的常规溶胶-凝胶法制备了70S30C生物活性玻璃。与传统方法相比,缩短了耗时。物理化学表征证实了合成玻璃是由相互连接的颗粒组成的非晶介孔结构材料。合成玻璃的比表面积为142.8 m2/g,孔体积为0.52 cm3/g,平均孔径为19.1 nm。此外,合成生物活性玻璃在模拟体液(SBF)溶液中浸泡1天后表现出有趣的生物活性,在细胞培养基中培养时表现出良好的生物相容性。
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Hydrothermal assisted conventional sol-gel method for synthesis of bioactive glass 70S30Cы
Bioactive glasses (Bioglasses) are widely synthesized by the conventional sol-gel method consisting of two main steps for sol and gel formation. However, the conversion from sol to gel requires a long time (5–7 days). In this study, the hydrothermal system was used to quickly synthesize the bioactive glass by reducing the conversion time from sol to gel. The hydrothermal assisted conventional sol-gel method was applied for synthesis of the bioactive glass 70SiO2–30CaO (mol%) (noted as 70S30C). The synthetic glass was investigated by the physical-chemical techniques. The ‘‘in vitro’’ experiments in SBF (Simulated Body Fluid) solution was also performed to evaluate the bioactivity of synthetic material. The obtained results show that the bioactive glass 70S30C was successfully elaborated by using the hydrothermal assisted conventional sol-gelmethod. The consuming time was reduced compared to the conventional method. The physical-chemical characterization confirmed that the synthetic glass is amorphous material with mesoporous structure consisting of interconnected particles.The specific surface area, pore volume and average pore diameter of synthetic glass were 142.8 m2/g, 0.52 cm3/g, and 19.1 nm, respectively. Furthermore, synthetic bioactive glass exhibited interesting bioactivity when immersed in simulated body fluid (SBF) solution for 1 days and good biocompatibility when cultured in cellular media.
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