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引用本文:梁键谋,傅聪,陈悦.LC-MS/MS测定草酸右旋西酞普兰中对甲苯磺酸酯类基因毒性杂质的含量[J].中国现代应用药学,2016,33(11):1436-1440.
LIANG Jianmou,FU Cong,CHEN Yue.Determination of Genotoxic Impurities in Escitalopram Oxalate by LC-MS/MS[J].Chin J Mod Appl Pharm(中国现代应用药学),2016,33(11):1436-1440.
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LC-MS/MS测定草酸右旋西酞普兰中对甲苯磺酸酯类基因毒性杂质的含量
梁键谋1, 傅聪2, 陈悦1
1.浙江省食品药品检验研究院, 杭州 310052;2.宁波医药高等专科学校, 宁波 317503
摘要:
目的 建立LC-MS/MS测定草酸右旋西酞普兰中对甲苯磺酸酯类基因毒性杂质的含量。方法 采用Zorbax Eclipse XDB C18(250 mm×4.6 mm,5 μm);流动相为20 mmol·L-1乙酸铵水溶液-乙腈,梯度洗脱,流速为0.8 mL·min-1;柱温为35℃;采用Ultimate 3000 HPLC-AB Science 4000 QTrap三重四极杆串联离子阱液质联用仪和多反应离子监测模式二级质谱MS/MS(ESI源)检测,正离子模式采集数据。结果 基因毒性杂质对甲苯磺酸乙酯和对甲苯磺酸异丙酯均在5~100 ng内与峰面积呈良好的线性关系,线性方程分别为y=1.19×104x-140(r=0.999 5)和y=1.27×103x-156(r=0.999 4),检测限分别为1 ng和2 ng,定量限分别为2 ng和4 ng,平均回收率分别为99.0%和101.0%;RSD分别为3.5%和4.7%(n=9)。结论 方法简便准确,可用于草酸右旋西酞普兰中对甲苯磺酸酯类基因毒性杂质的检测。
关键词:  草酸右旋西酞普兰  对甲苯磺酸乙酯  对甲苯磺酸异丙酯  基因毒性  液质联用
DOI:10.13748/j.cnki.issn1007-7693.2016.11.019
分类号:
基金项目:
Determination of Genotoxic Impurities in Escitalopram Oxalate by LC-MS/MS
LIANG Jianmou,FU Cong,CHEN Yue
Zhejiang Pharmaceutical College, Ningbo 317503, China
Abstract:
OBJECTIVE To establish an LC-MS/MS analytical method for the determination of genotoxic impurities in escitalopram oxalate. METHODS The method was achieved on a Zorbax Eclipse XDB C18 column(250 mm×4.6 mm, 5 μm) utilizing a mobile phase of 20 mmol·L-1 ammonium acetate(A)-acetonitrile(B) with gradient elution at the flow rate of 0.8 mL·min-1. The temperature of column was set at 35℃. The Ultimate 3000 HPLC-AB Science 4000 QTrap Tripling Four bar LC-MS was used to detect ethyl p-toluenesulfonate and isopropyl p-toluenesulfonate(ESI source, in Multiple Reaction Monitoring positive mode). RESULTS Standard curve was linear in the range of 5-100 ng(r=0.999 9). The limit of quantification of ethyl p-toluenesulfonate and isopropyl p-toluenesulfonate were separately 1 ng and 2 ng. The limit of detection were 2 ng and 4 ng, respectively. The average recovery of ethyl p-toluenesulfonate and isopropyl p-toluenesulfonate were 99.0% and 101.0%, RSD were 3.5% and 4.7%(n=9). CONCLUSION The method is convenient and sensitive for the determination of genotoxic impurities in escitalopram oxalate.
Key words:  escitalopram oxalate  ethyl p-toluenesulfonate  isopropyl p-toluenesulfonate  genotoxic impurities  LC-MS
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