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引用本文:袁抢云,陈程,李继超,何达仁,刘宗丽,任钢.HPLC测定奥美沙坦酯中的基因毒性杂质[J].中国现代应用药学,2017,34(3):407-409.
Yuan Qiangyun,Chen Cheng,Li Jichao,He Daren,Liu Zongli,Ren Gang.Determination of Genotoxic Impurity in Olmesartan Medoxomil by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2017,34(3):407-409.
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HPLC测定奥美沙坦酯中的基因毒性杂质
袁抢云1,2, 陈程2, 李继超2, 何达仁2, 刘宗丽2, 任钢2
1.浙江工业大学, 杭州 310014;2.浙江新赛科药业有限公司, 浙江 绍兴 312369
摘要:
目的 建立HPLC测定奥美沙坦酯中潜在的基因毒性杂质[杂质1N-(三苯基甲基)-5-(4'-溴甲基联苯-2-基)四氮唑,杂质2N-三苯甲基-5-(4',4'-二溴甲基联苯-2-基)四氮唑]的含量和限度。方法 采用Phenomenex C18柱(250 mm×4.6 mm,5 μm);流动相:0.1%冰乙酸水溶液-0.1%冰乙酸乙腈溶液(15:85);检测波长:254 nm;流速:1.5 mL·min-1;柱温:25℃。结果 杂质1 和杂质2 均在0.030 97~0.247 7 μg·mL-1内线性良好(r分别为0.999 6和0.998 7),平均回收率分别为94.37%和94.43%,RSD分别为2.38%和2.72%(n=9)。结论 该方法专属性强,准确、灵敏,可以作为奥美沙坦酯中基因毒性杂质1 和杂质2 的液相分析方法。
关键词:  奥美沙坦酯  基因毒性杂质  高效液相色谱法
DOI:10.13748/j.cnki.issn1007-7693.2017.03.023
分类号:R921.2
基金项目:
Determination of Genotoxic Impurity in Olmesartan Medoxomil by HPLC
Yuan Qiangyun1,2, Chen Cheng2, Li Jichao2, He Daren2, Liu Zongli2, Ren Gang2
1.Zhejiang University of Technology, Hangzhou 310014, China;2.Zhejiang Second Pharma Co., Ltd., shaoxing 312369, China
Abstract:
OBJECTIVE To establish a method of HPLC to determine the limit and content of potential genotoxic impurities:N-(triphenylmethyl)-5-(4'-bromomethylbiphenyl-2-yl-) tetrazole (impurity 1), and N-(triphenylmethyl)-5-[4',4'-(dibromomethylbiphenyl)-2-yl]tetrazole (impurity 2) in active pharmaceutical substance Olmesartan Medoxomil qualitatively and quantitatively. METHODS The method was performed on Phenomenex C18 column (250 mm×4.6mm, 5 μm). And 0.1% glacial acetic acid in water (A):0.1% glacial acetic acid dissolved in acetonitrile (B) as the mobile phase which was 15:85 with a flow rate at 1.5 mL·min-1. The detection wavelength was 254 nm, and the temperature of column was 25℃. RESULTS The calibration curve for impurity 1 and impurity 2 was well linear in the range of 0.030 97-0.247 7 μg·mL-1(rwas 0.999 6 and 0.998 7, respectively). Average recovery for impurity 1 and impurity 2 was 94.37% and 94.43%, and RSD was 2.38% and 2.72%(n=9), separately. CONCLUSION The method is highly specific, accurate and sensitive, it can be used for the quality control of the genotoxic impurities 1 and impurities 2 of Olmesartan Medoxomil.
Key words:  Olmesartan Medoxomil  genotoxic impurity  HPLC
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