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西沙必利在新型键合手性柱上的拆分及其在血浆中的含量测定
引用本文:周婕,郑旭霞,孙芳,赵素珍,李欣雨,张振中.西沙必利在新型键合手性柱上的拆分及其在血浆中的含量测定[J].郑州大学学报(自然科学版),2014(2):93-98.
作者姓名:周婕  郑旭霞  孙芳  赵素珍  李欣雨  张振中
作者单位:[1]郑州大学药学院,河南郑州450001 [2]药物关键制备技术省部共建重点实验室,河南郑州450001
摘    要:建立一种用新型键合纤维素手性固定相拆分西沙必利对映体的高效液相色谱方法,并利用此方法测定血浆中西沙必利的含量.使用Chiralpak IC色谱柱(250 mm×4.6 mm,5μm),流动相为正己烷-异丙醇-二乙胺(体积比80∶ 20∶0.1),流速0.8 mL/min,检测波长273 nm,柱温25℃.取血浆200 μL,加入西沙必利标准溶液10 μL,碱化后用正庚烷-异戊醇(体积比95∶5)提取,40℃氮气吹干.结果表明:西沙必利对映体在新型键合直链纤维素衍生化合物手性固定相上能够完全分离,分离度为1.65;其血浆提取回收率达87%,线性范围为10~ 160 μg/mL,最低检测限为5 μg/mL,RSD<4.0%.本方法可方便地实现西沙必利对映体的分离及其在血浆中的含量测定,为临床上西沙必利的血药浓度监测及药代动力学研究提供了便捷、灵敏的分析手段.

关 键 词:高效液相色谱法  Chiralpak  IC手性柱  对映体分离  西沙必利  含量测定  血浆

Separation and Quantitative Determination of Cisapride Enantiomers on a New Cellulose Bonded Chiral Stationary Phase
ZHOU Jie,ZHENG Xu-xia,SUN Fang,ZHAO Su-zhen,LI Xin-yu,ZHANG Zhen-zhong.Separation and Quantitative Determination of Cisapride Enantiomers on a New Cellulose Bonded Chiral Stationary Phase[J].Journal of Zhengzhou University (Natural Science),2014(2):93-98.
Authors:ZHOU Jie  ZHENG Xu-xia  SUN Fang  ZHAO Su-zhen  LI Xin-yu  ZHANG Zhen-zhong
Institution:1.School of Pharmacy,Zhengzhou University,Zhengzhou 450001,China;Key Laboratory of State Ministry of Education for Pharmaceutical Technology,Zhengzhou 450001,China)
Abstract:A liquid chromatographic method for the chiral separating enantiomers of cisapride in plasma was developed.Cisapride enantiomers were separated and determinated by a Chiralpak IC chiral column (250 mm ×4.6 mm,5 μm) at 25 ℃ and detected at 273 nm,the mobile phase used was n-hexane-isopropanol (80∶ 20,0.1% DEA) at a flow rate of 0.8 mL/min.Alkalinized samples of plasma (200 μL) were extracted with n-heptane-isopentanol (95∶ 5).The organic phase was evaporated to dryness under nitrogen at 40 ℃.The results showed that cisapride enantiomers were separated on a new cellulose bonded chiral stationary phase and the resolution was 1.65.The mean extraction efficiency was 87%.Calibration plots in rat plasma were linear from 10 to 160 μg/mL.The limit of detection was 5 μg/mL and RSD <4.0%.The present method could be easily used for separating the enantiomers of cisapride and determination of cisapride enantiomers in plasma.It provided a new approach for the determination of plasma concentration and its pharmacokinetic studies.
Keywords:HPLC  Chiralpak IC chiral column  enantiomeric separation  cisapride  quantitative determination  plasma
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