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建立一种用于测定绵羊血浆中醋酸氟孕酮的高效液相色谱-串联质谱法。

Development of a high-performance liquid chromatography-tandem mass spectrometry method for the determination of flurogestone acetate in ovine plasma.

作者信息

Monnoyer S, Capancioni S, Richard M, Pacaud M, Guyonnet J

机构信息

CEVA Santé Animale, Pre-clinical Development, La Ballastière, B.P. 126, 33501 Libourne Cedex, France.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 May 25;819(2):245-51. doi: 10.1016/j.jchromb.2005.01.028.

Abstract

Flurogestone (FGA) is a synthetic progesterone, with a progestational action higher than that of progesterone itself. It is intended for vaginal use in large animals to induce oestrus synchronization. A quantitative method for the analysis of flurogestone acetate (FGA) in ovine plasma by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) has been developed. After the incorporation of megestrol acetate (MGA) as internal standard (IS) and followed by a liquid-liquid extraction from plasma, FGA and MGA were chromatographed using a reverse-phase HPLC column and detected by tandem mass spectrometry with a TurboIonSpray source. Multiple reaction-monitoring (MRM) mode was used for the quantitative determination of FGA in ovine plasma. The precursor ions M+H at m/z 407.2 and 385.1 for FGA and MGA, respectively, produced product ions at m/z 267.1/285.1 for FGA and m/z 267.1/224.0 for MGA. The validated concentration range was 0.2-5.0 ng/ml based on 500 microl plasma aliquots. The lower limit of quantitation was 0.2 ng/ml. Fully validated selectivity, accuracy, precision and reproducibility criteria for routine use in pharmacokinetic studies were demonstrated.

摘要

氟孕酮(FGA)是一种合成孕激素,其孕激素作用高于孕酮本身。它用于大型动物的阴道给药以诱导发情同步。已开发出一种通过高效液相色谱 - 串联质谱法(HPLC-MS/MS)分析绵羊血浆中醋酸氟孕酮(FGA)的定量方法。加入醋酸甲地孕酮(MGA)作为内标(IS)后,接着从血浆中进行液 - 液萃取,FGA和MGA使用反相HPLC柱进行色谱分离,并通过带有TurboIonSpray源的串联质谱进行检测。采用多反应监测(MRM)模式对绵羊血浆中的FGA进行定量测定。FGA和MGA的前体离子M + H分别在m/z 407.2和385.1,FGA产生的产物离子为m/z 267.1/285.1,MGA产生的产物离子为m/z 267.1/224.0。基于500微升血浆等分试样,验证的浓度范围为0.2 - 5.0 ng/ml。定量下限为0.2 ng/ml。证明了该方法在药代动力学研究中常规使用的完全验证的选择性、准确性、精密度和重现性标准。

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