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作 者:孙丹丹[1] 闫雪生[1] 徐新刚[1] 于蓓蓓[1] 生立嵩[1]
出 处:《辽宁中医药大学学报》2016年第1期56-59,共4页Journal of Liaoning University of Traditional Chinese Medicine
基 金:山东省科技发展计划项目(2011GSF11902)
摘 要:目的:制备熊果酸自微乳冻干制剂并进行体外评价。方法:制备熊果酸自微乳冻干制剂,考察其形态、粒径分布、Zeta电位、p H值、电导率、折光率、黏度、稳定性及体外释放度等。结果:熊果酸自微乳冻干制剂在透射电镜下成球状或类球状,平均粒径为34.5 nm,Zeta电位为-9.72,p H值为5.72,电导率为16.2μs·cm^(-1),折光率为1.3354,黏度为2.4 m Pa·s,冻干制剂在6个月内稳定性良好,与药物溶液相比,熊果酸自微乳制剂在体外具有一定缓释效果。结论:熊果酸自微乳冻干制剂物理和化学稳定性良好,体外释药表明熊果酸自微乳制剂呈现一定的缓释效果。Objective:To investigate the preparation and in vitro evaluation of Ursolicacid(UA)self-microemulsion after freeze-drying. Methods:The quality of the UA self-microemulsion was evaluated after freeze-drying. Including partical size and its distribution,configuration,Zeta potential,p H,viscosity,refractive,conductivity,releasing characteristic in vitro and stability. Results:The selfmicroemulsion was spheroidal shape through observing by transmission electron microscopy,the mean partical size was 34.5 nm,the Zeta potential was-9.72,the p H value was 5.72,the conductivity was 16.2 μs·cm^(-1),the refractive was 1.3354,the viscosity was 2.4 m Pa·s,the stability test showed that the properties of the preparation were stable in six mounths after freeze-drying,and releasing characteristic in vitro showed prolonged release characteristic. Conclusion:The stability experiments indicate that the physical and chemical stability of the UA self-microemulsion is favorable after freezedrying. Comparing with UA solution,UA self-microemulsion exhibited a certain delayed release profile.
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