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格列齐特缓释片的研制及体外释放度考察
引用本文:赵丽华,胡容峰,李华,李嘉煜,李师,梅康康.格列齐特缓释片的研制及体外释放度考察[J].中国药房,2006,17(18):1382-1384.
作者姓名:赵丽华  胡容峰  李华  李嘉煜  李师  梅康康
作者单位:1. 安徽省现代中药研究中心,合肥市,230038;安徽中医学院药剂教研室,合肥市,230038;武警安徽总队医院药械科,合肥市,230041
2. 安徽省现代中药研究中心,合肥市,230038;安徽中医学院药剂教研室,合肥市,230038
3. 安徽省现代中药研究中心,合肥市,230038
摘    要:目的;制备格列齐特缓释片并考察其体外释放度。方法采用混合骨架材料制备格列齐特缓释片;参照进口格列齐特缓释片标准,采用紫外分光光度法,以pH7.4磷酸盐缓冲液900ml为溶剂,桨法测定本品释放度,并与参比制剂进行比较。结果所得缓释片体外释放度符合一级动力学规律,释放曲线经相似因子(f2)判断,与参比制剂相似。结论本品处方工艺稳定、重现性好,体外累积释放度符合要求。

关 键 词:格列齐特缓释片  制备  混合骨架材料  释放度
文章编号:1001-0408(2006)18-1382-03
修稿时间:2006年1月1日

Preparation and Dissolution of Gliclazide Sustained Release Tablets in Vitro
ZHAO Lihua,HU Rongfeng,LI Hua,LI Jiayu,LI Shi,Mei Kangkang.Preparation and Dissolution of Gliclazide Sustained Release Tablets in Vitro[J].China Pharmacy,2006,17(18):1382-1384.
Authors:ZHAO Lihua  HU Rongfeng  LI Hua  LI Jiayu  LI Shi  Mei Kangkang
Abstract:OBJECTIVE:To prepare gliclazide sustained release tablets,and to evaluate its dissolution in vitro.METHODS:Mixed matrix materials was used to prepare the tablet.According to the standard of imported Gliclazide sustained release tablets,the dissolution was determined by UV-absorption spectrometry in release medium of900ml of phosphate buffer with pH value of7.4(paddle method).The results were compared with those of the reference preparation.RESULTS:The dissolution of the prepared tablet in vitro accorded with the first order kinetics law.The release curve was similar to that of reference preparation judging from similar agent(f 2 ).CONCLUSION:The formula of this preparation is stable in technology,good in reproduction quality,and presents a standard cumulative dissolution in vitro.
Keywords:Gliclazide sustained release tablet  Preparation  Mixed matrix materials  Dissolution
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