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引用本文:秦斌,谭志欣,殷果,周远波,闫研.富马酸酮替芬片溶出度的测定[J].中国现代应用药学,2015,32(1):72-75.
QIN Bin,TAN Zhixin,YIN Guo,ZHOU Yuanbo,YAN Yan.Dissolution Determination of Ketotifen Fumarate Tablets[J].Chin J Mod Appl Pharm(中国现代应用药学),2015,32(1):72-75.
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富马酸酮替芬片溶出度的测定
秦斌1,2, 谭志欣3, 殷果1,2, 周远波4, 闫研1,2
1.深圳药品质量标准研究重点实验室,广东 深圳 518057;2.深圳市药品检验所,广东 深圳 518029;3.广州市胸科医院,广州 510095;4.广东药学院,广东 东莞 523808
摘要:
目的 建立富马酸酮替芬片溶出度测定方法。方法 采用浆法,以水900 mL为溶出介质,转速50 r·min-1,Inertsil ODS-SP色谱柱(4.6 mm×250 mm,5 μm),以甲醇-水-三乙胺(950∶50∶0.02)为流动相,检测波长:300 nm。结果 富马酸酮替芬的浓度在0.1~25 μg·mL-1内与峰面积线性关系良好,回收率为99.9%,RSD为0.1%。结论 该溶出度实验条件可以较客观地反映产品的内在品质,对不同来源的同一制剂具有显著的区分力。
关键词:  富马酸酮替芬片  溶出度  浆法  高效液相色谱法
DOI:
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基金项目:
Dissolution Determination of Ketotifen Fumarate Tablets
QIN Bin1,2, TAN Zhixin3, YIN Guo1,2, ZHOU Yuanbo4, YAN Yan1,2
1.Shenzhen Key Laboratory of Drug Quality Standard Research, Shenzhen 518057, China;2.Shenzhen Institute for Drug Control, Shenzhen 518029, China;3.Guangzhou Chest Hospital, Guangzhou 510095, China;4.Guangdong Medical College, Dongguan 523808, China
Abstract:
OBJECTIVE To establish an HPLC method for the determination of the dissolution of Ketotifen Fumarate tablets. METHODS The paddle method was used with 900 mL water as dissolution medium at the rotate speed of 50 r·min-1. Inertsil ODS-SP column(4.6 mm×250 mm, 5 μm) was used with the mobile phase of methanol-water-triehylamine(950∶50∶ 0.02) at the detection wavelength of 300 nm. RESULTS The calibration curve of ketotifen fumarate was linear in the ange of 0.1-25 μg·mL-1. The average recovery was 99.9% with RSD of 0.1%. CONCLUSION The inherent quality of the product can be objectively reflected in the above conditions. Furthermore, it has a significant distinction of the same agents from different sources.
Key words:  Ketotifen Fumarate tablets  dissolution  paddle method  HPLC
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