• 首页期刊简介编委会刊物订阅专栏专刊电子刊广告合作联系我们English
引用本文:郑一美,苗飞,周福富,王平.柱前衍生化GC测定佐芬普利钙中间体光学杂质[J].中国现代应用药学,2016,33(3):335-338.
ZHENG Yimei,MIAO Fei,ZHOU Fufu,WANG Ping.Determination of Optical Isomer Impurity in the Intermediate of Zofenopril Calcium by GC with Pre-column Derivatization[J].Chin J Mod Appl Pharm(中国现代应用药学),2016,33(3):335-338.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 2300次   下载 2010 本文二维码信息
码上扫一扫!
分享到: 微信 更多
柱前衍生化GC测定佐芬普利钙中间体光学杂质
郑一美1, 苗飞2, 周福富1, 王平3
1.金华职业技术学院,浙江 金华 321000;2.浙江华海药业有限公司,浙江 台州 317000;3.浙江工业大学药学系,杭州 310014
摘要:
目的 建立测定佐芬普利钙中间体(S)-(-)-3-苯甲酰巯基-2-甲基丙酸的光学异构体杂质(R)-(+)-3-苯甲酰巯基-2-甲基丙酸含量的柱前衍生化GC。方法 以高纯试剂D-(+)-2-辛醇对(S)-(-)-3-苯甲酰巯基-2-甲基丙酸样品进行衍生化处理,衍生产物以Agilent DB-1701(30 m×0.53 mm,1.0 μm)柱为分析柱,以氮气为载气,流速为2.0 mL·min-1,检测器温度为250 ℃,进样口温度为200 ℃,柱温为程序升温,进样量为1.0 μL。结果 光学杂质(R)-(+)-3-苯甲酰巯基-2-甲基丙酸在3.22~121.44 μg·mL-1内线性关系良好(r=0.995 2),定量限为3.22 μg·mL-1,加样回收率为99.6%~102.4%,日内和日间精密度RSD均<2.0%。结论 该方法操作简便、专属性强,试剂成本低廉、易得,结果准确性高、重复性好,可用于佐芬普利钙中间体(S)-(-)-3-苯甲酰巯基-2-甲基丙酸光学杂质的含量测定。
关键词:  佐芬普利钙  中间体  光学杂质  气相色谱法  柱前衍生化
DOI:
分类号:
基金项目:
Determination of Optical Isomer Impurity in the Intermediate of Zofenopril Calcium by GC with Pre-column Derivatization
ZHENG Yimei1, MIAO Fei2, ZHOU Fufu1, WANG Ping3
1.Jinhua Polytechnic, Jinhua 321000, China;2.Zhejiang Huahai Pharmaceutical Co., Ltd., Taizhou 317000, China;3.College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China
Abstract:
OBJECTIVE To establish a method for the quantitative determination of optical isomer impurity in the intermediate of zofenopril calcium by GC with pre-column derivatization. METHODS Using D-(+)-2-Octanol as pre-column derivatization reagent, the optimal chromatographic separation was performed on Agilent DB-1701(30 m×0.53 mm, 1.0 μm) column with nitrogen as the carrier gas at a flow rate of 2.0 mL·min-1, the detector temperature was at 250 ℃, the inlet temperature was at 200 ℃. The temperature program was used. The injection volume was 1.0 μL. RESULTS The calibration curve was good linear relationship in the range of 3.22-121.44 μg·mL-1 for the optical isomer impurity (R)-(+)-3-benzoyl thiol-2-methyl propionate(r=0.995 2). The limit of quantification was 3.22 μg·mL-1. The average recovery was 99.6%-102.4%. The RSD of intra and inter day were <2.0%. CONCLUSION The method is simple, specific and accurate with good repeatability, which can be used for the determination of optical isomer impurity in the intermediate of zofenopril calcium.
Key words:  zofenopril calcium  intermediate  optical impurity  GC  pre-column derivatization
扫一扫关注本刊微信