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利巴韦林缓释片的制备及其释放度测定
引用本文:杨伟俊,罗玉琴,邢建国,于富生,戴秀勇.利巴韦林缓释片的制备及其释放度测定[J].中国医院药学杂志,2005,25(7):628-631.
作者姓名:杨伟俊  罗玉琴  邢建国  于富生  戴秀勇
作者单位:1. 新疆药物研究所,新疆,乌鲁木齐,830002
2. 新疆华世丹药物研究有限公司,新疆,乌鲁木齐,830011
摘    要:目的:制备利巴韦林缓释片,对其释放机制进行考察.方法:建立高效液相色谱(HPLC)体外释放度测定法,以羟丙基甲基纤维素(HPMC)为主要辅料,制备亲水凝胶型骨架片,采用单因素试验筛选辅料种类,通过均匀设计优化出缓释片的处方.结果:所制备的缓释片在8 h内呈良好的零级释药特征.结论:以均匀设计优选的利巴韦林缓释片处方合理,体外释放性能良好.

关 键 词:利巴韦林  缓释片  释放度  均匀设计
文章编号:1001-5213(2005)07-0628-04
收稿时间:2004-07-27
修稿时间:2004年7月27日

Preparation of ribavrin sustained release tablets and its drug release
YANG Wei-jun,LUO Yu-qin,XING Jian-guo,YU Fu-sheng,DAI Xiu-yong.Preparation of ribavrin sustained release tablets and its drug release[J].Chinese Journal of Hospital Pharmacy,2005,25(7):628-631.
Authors:YANG Wei-jun  LUO Yu-qin  XING Jian-guo  YU Fu-sheng  DAI Xiu-yong
Abstract:OBJECTIVE To prepare ribavirin sustained release tablets and investigate its release mechanism in vitro. METHODS To establish a HPLC method for determing the content of ribavirin. The water-soluble matrix tablet was preparaed by use of HPMC.The optimal formulation was obtained by uniform design. RESULTS The release profile of the tablets in vitro was fitted well by zeros-order release within 8 hours. CONCLUSION The formulation and the release mechanism in vitro is reasonable.
Keywords:ribavirin  sustained release tablet  drug release  uniform design
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