三七总皂苷肠溶微囊的制备及体外释放度  

Preparation and in vitro Release of Panax notoginseng Saponins Enteric Microcapsules

作　　者：陆仕华[1] 刘华钢[1] 赖玲[1] 秦艳娥[1] 文丽[2] 陈明 刘冠萍 

机构地区：[1]广西医科大学药学院,南宁530021 [2]广西中医学院,南宁530001 [3]广西梧州制药(集团)股份有限公司,广西梧州543000

出　　处：《中国实验方剂学杂志》2011年第14期11-14,共4页Chinese Journal of Experimental Traditional Medical Formulae

基　　金：广西企业科技特派员专项(桂科攻09321049);广西自然科学基金项目(2010GXNSFB013068)

摘　　要：目的:探讨三七总皂苷(PNS)肠溶微囊的制备方法,并对其进行体外释放度研究。方法:以聚丙烯酸树脂Ⅱ为囊材,采用溶剂-非溶剂法制备PNS肠溶微囊,并考察其包封率、载药量及其体外释放性能。结果:3批PNS肠溶微囊的包封率分别为90.85%,90.15%,89.06%;载药量分别为26.05%,25.04%,25.16%;R1,Rg1,Rb1在人工胃液中释放量<10%,人工肠液中45 min累积释放率分别达到86.08%,88.76%,84.98%。结论:溶剂-非溶剂法制备PNS肠溶微囊方法简单,体外释放符合药典对肠溶制剂的要求。Objective：To study the preparation method of PNS enteric microcapsules and to investigate the release properties in vitro.Method： The solvent-non-solvent extraction was used to prepare enteric microcapsule of PNS with the polyacrylic acid resin II as the pouch material.The encapsulation efficacy and loading efficiency as well as the properties in vitro release of PNS enteric microcapsules were investigated.Result： Encapsulation efficiency was 90.85%,90.15%,and 89.06%,loading efficiency was 26.05%,25.04%,and 25.16% respectively.The release of R1,Rg1 and Rb1 was less than 10% in the artificial gastric juices,and up to 86.08%,88.76%,and 84.98% in the artificial intestinal juices after 45 min.Conclusion： The microcapsules meet the requirements of pharmacopoeia in vitro release.

关 键 词：三七总皂苷 肠溶微囊 溶剂-非溶剂法 释放度 

分 类 号：R283.6[医药卫生—中药学]