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机构地区:[1]上海恒瑞医药有限公司,上海200245 [2]上海食品药品监督管理局科技情报研究所,上海200233
出 处:《中国中药杂志》2009年第20期2590-2593,共4页China Journal of Chinese Materia Medica
摘 要:目的:制备冬凌草甲素亚微乳,并对其理化性质进行表征。方法:采用高压均质法制备冬凌草甲素亚微乳,并对其粒径、Zeta电位、黏度等性质进行表征。结果:冬凌草甲素亚微乳为白色不透明乳状液体,载药量1g·L-1,平均粒径(138.87±0.60)nm,Zeta电位(47.27±2.31)mV,pH(6.02±0.03),黏度(1.78±0.015)MPa.s。结论:本实验所制得的冬凌草甲素亚微乳理化性质较稳定,工艺简单,可为冬凌草甲素亚微乳制剂的制备提供研究依据。Objective:To prepare the oridonin submicron emulsion and characterize their properties. Method:High pressure homogenization method was employed to prepare the oridonin submicron emulsion and such properties as size,Zeta potential and viscosity were characterized. Result:The results showed that the submicron emulsions was formed with the drug loading 1 g·L^-1,particle size of (138.87±0.60) nm,zeta potential of (47.27±2.31) mV,pH value of (6.02±0.03) and viscosity of (1.78±0.015) MPa·s,respectively. Conclusion:The method is feasible and the submicron emulsions has stable properties. Experiments offer a new formulation of oridonin for clinical application.
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