中成药2017，Vol.39Issue(11)：2284-2288,5.DOI:10.3969/j.issn.1001-1528.2017.11.012
甘草酸二铵二元脂质体温敏凝胶的制备及其体外释药行为
Preparation of thermo-sensitive diammonium glycyrrhizinate binary liposome gel and the in vitro drug-release behaviors
薛晶 1高苑 1王新蕾 1刘芳 1郝保华1
作者信息
- 1. 西北大学生命科学学院,陕西西安710069
- 折叠
摘要
Abstract
AIM To prepare thermo-sensitive diammonium glycyrrhizinate binary liposome gel and to evaluate the in vitro drug-release behaviors.METHODS Cold dissolution method was adopted in the preparation of gel.With gel transition temperature as an evaluation index,amounts of Poloxamer 407 (P407),Poloxamer 188 (P188) and polysaccharides from Bletillae Rhizoma as influencing factors,central composite design-response surface method was applied to optimizing the formulation.Then the in vitro drug-release behaviors were evaluated by HPLC and Franz vertical diffusion cell method.RESULTS The optimal formulation was determined to be 18％ for P407 amount,4％ for P188 amount,and 0.6％ for polysaccharides' amount,the gel transition temperature was (37.5 ± 0.3) ℃.The accumulative release rate of obtained thermo-sensitive binary liposome gel was (65.52 ± 0.63) ％ within 48 h,which showed more obvious sustained-release effect as compared with liposome and thermosensitive gel.CONCLUSION Thermo-sensitive diammonium glycyrrhizinate binary liposome gel can reduce drug-release rate and increase its retention time in the rectum.关键词
甘草酸二铵/二元脂质体/温敏凝胶/体外释药行为/冷溶法/星点设计-效应面法/HPLC/Franz立式扩散池法Key words
diammonium glycyrrhizinate/binary liposome/thermo-sensitive gel/in vitro drug-release behaviors/cold dissolution method/central composite design-response surface method/HPLC/Franz vertical diffusion cell method分类
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薛晶,高苑,王新蕾,刘芳,郝保华..甘草酸二铵二元脂质体温敏凝胶的制备及其体外释药行为[J].中成药,2017,39(11):2284-2288,5.
