期刊文献+

阿托伐他汀钙分散片溶出度的测定 被引量:4

Dissolution Determination of Atorvastatin Calcium Dispersible Tablets
下载PDF
导出
摘要 目的建立阿托伐他汀钙分散片溶出度的测定方法。方法以水为溶出介质,采用浆法(50r/min)30min取样,运用紫外-可见分光光度法测定溶出度,并考察了溶出曲线。结果样品溶出均一性良好,溶出度均>90%。结论本法可用于测定阿托伐他汀钙分散片的溶出度。 Objective To establish a method to determine the dissolution of Atorvastatin Calcium Dispersible Tablets. Methods The oar method (50 r/min) was adopted with the dissolution medium of water and sampling after 30 minutes. The dissolution was determined by UV. The dissolution curve was investigated. Results The dissolution homogeneity of three batches of samples was good and dissolution was all above 90 percent. Conclusion This method can be used to investigate and control the quality of Atorvastatin Calcium Dispersible Tablets.
出处 《食品与药品》 CAS 2006年第11A期49-51,共3页 Food and Drug
关键词 阿托伐他汀钙分散片 溶出度 测定 Atorvastatin Calcium Dispersible Tablets dissolution determination
  • 相关文献

参考文献4

二级参考文献4

  • 1李健斋.降胆固醇防治冠心病:新认识与新动向[J].中华老年医学杂志,1996,15(6):325-327. 被引量:14
  • 2Bullen WW,Miller RA,Hayes RN, et al. Development and validation of a high-performance liquid chromatography tandem mass spectrometry assay for atorvastatin, ortho-hydroxy atorvastatin,and para-hydroxy atorvastatin in human,dog,and rat plasma[J].J Am Soc Mass Spectrom, 1999,10(1 ) : 55.
  • 3Jemal M,Ouyang Z,Chen BC, et al. Quantitation of the acid and lactone forms of atorvastatin and its biotransformation products in human serum by high-performance liquid chromatography with electrospray tandem mass spectrometry [ J ]. Rapid Commun Mass Spectrom, 1999,13(11) : 1003.
  • 4李健斋,傅得兴.高效他汀类降血脂新药阿托他汀[J].中国新药杂志,1999,8(5):294-298. 被引量:30

共引文献56

同被引文献29

引证文献4

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部