摘要: |
[目的]确定脑康通泰分散片的处方工艺,并建立其溶出度测定方法。并与自制普通剂型进行溶出度比较。[方法]以休止角、硬度、崩解时限、颗粒流动性等为指标考察处方,优化后确定终处方。采用2010年版中国药典二部附录溶出度测定法,以900 mL水为溶出介质,转速为100 r/min,并于270 nm波长处测定吸收度。[结果]优选出最佳处方:24%磷酸氢钙和20%微晶纤维素为填充剂,10%交联聚维酮与2%二氧化硅为混合崩解剂,1%硬脂酸镁为润滑剂,分散片的崩解时限小于3 min。30 min内溶出度不低于75%。[结论]湿法制粒压片制备脑康通泰分散片处方合理,工艺简单,溶出度测定方法结果准确,质量可控,开发脑康通泰分散片具有临床意义。 |
关键词: 脑康通泰分散片 制备工艺 溶出度 |
DOI:10.11656/j.issn.1672-1519.2011.05.27 |
分类号: |
基金项目:国家重点基础研究发展计划项目(2010CB735602) |
|
Determination of preparation and dissolution with Naokangtongtai dispersible tablet |
WANG Wei1, LI Hong-qi2, ZOU Jun-zhong3
|
1.Tianjin University of TCM, Tianjin 300193, China;2.State Key Laboratory of Drug Delivery Technology and Pharmacokinetics, Tianjin 300193, China;3.Tianjin Institute of Pharmaceutical Research, Tianjin 300193, China;4.TIPR Pharmaceutical Responsible Co.,Ltd, Tianjin 300193, China
|
Abstract: |
[Objective] To prepare Naokangtongtai dispersible tablets and establish the dissolution method.To compare with the dissolution of other common products.[Methods] The formulation of the tablets was optimized through the indices: slope of repose,hardness,disintegration time and corpuscular liquidity.Dissolution was determined by the solvent according to the method in Chinese Pharmacopoeia(2010,Appendix Ⅱ) with 900 mL water as the solvent at a rotation speed of 100 r/min.And the detection wavelength was 270 nm.[Results] The proportion of each adjuvant in the optimal formulation consisted of 20% microcrystalline cellulose and 24% brushite as a filler,and 10% crospovidone mixed with 2% silicon dioxide as disintegrating agent,1% magnesium stearate as lubricants.The dispersible tablets could disintegrate completely within 3 minutes and its dissolution rate could reach beyond 75% in 30 min.[Conclusion] The preparative method of Naokangtongtai dispersible tablets by wet granulation is simple.The method is accurate and suitable for the dissolution determination of Naokangtongtai dispersible tables. |
Key words: Naokangtongtai dispersible tablets preparation technology dissolution |