首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Quantitative determination of pimozide in human plasma by liquid chromatography-mass spectrometry and its application in a bioequivalence study.
【24h】

Quantitative determination of pimozide in human plasma by liquid chromatography-mass spectrometry and its application in a bioequivalence study.

机译:液相色谱-质谱联用法定量测定人血浆中的匹莫嗪及其在生物等效性研究中的应用。

获取原文
获取原文并翻译 | 示例
           

摘要

A simple, sensitive and specific LC-ESI/MS method was developed for the determination of pimozide in human plasma. Pimozide and cinnarizine (internal standard) were isolated from plasma samples by liquid-liquid extraction. The chromatographic separation was accomplished on a Thermo Hypersil-HyPURITY C18 reversed-phase column (150mmx2.1mm, i.d., 5microm) with the mobile phase consisting of 5mM ammonium acetate (pH 3.5, adjusted with acetic acid)-methanol-acetonitrile (39:5:56, v/v/v). The lower limit of quantification was 0.02ng/mL, and the assay exhibited a linear range of 0.025-12.800ng/mL. The established method has been successfully applied to a bioequivalence study of 2 pimozide formulations in 32 healthy male Chinese volunteers.
机译:开发了一种简单,灵敏且特异的LC-ESI / MS方法,用于测定人血浆中的匹莫嗪。通过液-液萃取从血浆样品中分离出吡莫嗪和肉桂利嗪(内标)。色谱分离是在Thermo Hypersil-HyPURITY C18反相柱(150mmx2.1mm,内径,5微米)上完成的,流动相由5mM乙酸铵(pH 3.5,用乙酸调节)-甲醇-乙腈(39: 5:56,v / v / v)。定量下限为0.02ng / mL,测定线性范围为0.025-12.800ng / mL。所建立的方法已成功地应用于32名健康的中国男性志愿者中2种匹莫嗪制剂的生物等效性研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号