正交设计优化甲磺酸地拉韦啶分散片处方
投稿时间:2008-04-28    点此下载全文
引用本文:管清香,林天慕,王恩思.正交设计优化甲磺酸地拉韦啶分散片处方[J].药学实践杂志,2008,(4):261~263,277
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作者单位E-mail
管清香 吉林大学药学院,吉林,长春130021
吉林大学生命科学学院,吉林,长春130013 
wangss@jlu.edu.cn 
林天慕 吉林大学生命科学学院,吉林,长春130013  
王恩思 吉林大学药学院,吉林,长春130021
吉林大学生命科学学院,吉林,长春130013 
 
基金项目:吉林省卫生厅重点实验室项目(2005055)
中文摘要:目的:筛选甲磺酸地拉韦啶薄膜衣分散片的处方并进行制备。方法:以崩解时限为指标,采用正交设计实验,对分散片处方进行筛选,并进行体外溶出度考察。结果:按优选处方制备的3批分散片外观光洁,均在3 min内完全崩解并通过710μm筛。结论:研制的甲磺酸地拉韦啶分散片处方合理、工艺可行,符合分散片的质量要求。
中文关键词:甲磺酸地拉韦啶  分散片  体外溶出度
 
The formula optimization of delavirdine mesylate dispersible tablets by orthogonal design test
Abstract:Objective:To optimize the formula and prepare delavirdine mesylate dispersible tablets.Methods:The formula of delavirdine mesylate dispersible tablet was optimized in term of disintegrating time by orthogonal design test.The dissolution rates of the principal agent in dispersible tablets were determined.Results:The optimized dispersible tablets had fine appearance and disintegrated in 3 min,and the suspension screened through the 710μm mesh.The dissolution rates of the dispersible tablets were similar in 3 bat- ches formulation.Conclusion::The prepared delavirdine mesylate dispersible tablet was reasonable in formula,feasible in technology and was accorded with the quality standards.
keywords:delavirdine mesylate  dispersible tablet  dissolution rate in vitro
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