http://jcps.bjmu.edu.cn

中国药学(英文版) ›› 2017, Vol. 26 ›› Issue (8): 589-594.DOI: 10.5246/jcps.2017.08.066

• 【研究论文】 • 上一篇    下一篇

高效液相色谱法测定beagle犬血浆中达比加群浓度及达比加群酯纳米混悬剂药物动力学研究

从双晨, 张媛媛, 雷冏茜, 宋茂远, 张文茜, 彭光华, 殷梦雅, 李佳佳, 王佳星, 李馨儒*   

  1. 北京大学医学部 药学院 分子药剂学与新释药系统北京市重点实验室, 北京 100191
  • 收稿日期:2017-04-18 修回日期:2017-05-20 出版日期:2017-08-31 发布日期:2017-06-15
  • 通讯作者: Tel.: +86-010-82801508, E-mail: ll@bjmu.edu.cn
  • 基金资助:
    The National Basic Research Program of China (Grant No. 2015CB932100).

Determination of dabigatran in dog plasma by LC-MS/MS and its application to a pharmacokinetic study of dabigatran etexilate nanosuspension

Shuangchen Cong, Yuanyuan Zhang, Jiongxi Lei, Maoyuan Song, Wenxi Zhang, Guanghua Peng, Mengya Yin, Jiajia Li, Jiaxing Wang, Xinru Li*   

  1. Beijing Key Laboratory of Molecular Pharmaceutics and New Drug System; School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China

  • Received:2017-04-18 Revised:2017-05-20 Online:2017-08-31 Published:2017-06-15
  • Contact: Tel.: +86-010-82801508, E-mail: ll@bjmu.edu.cn
  • Supported by:
    The National Basic Research Program of China (Grant No. 2015CB932100).

摘要:

本研究建立了一种快速、灵敏的定量方法, 检测beagle犬口服达比加群酯纳米混悬剂后血浆中达比加群的浓度采用液-质谱/质谱方法, 使用反相C18, 以甲醇甲酸缓冲液为流动相进行梯度洗脱, 以盐酸舍曲林为内标, 流速为0.4 mL/min。达比加群[M+H]+m/z 472.17→289.07, 舍曲林[M+H]+m/z 305.98→275.00, 正离子模式, 质谱多反应监测扫描方式检测样品中达比加群的浓度。研究结果表明, 达比加群在1.0–500 ng/mL浓度范围内具有良好线性(r = 0.9995), 准确度在94.8%–107.1%之间, 精密度偏差在±6%之内。该方法可成功应用于达比加群酯纳米混悬剂beagle犬的药代动力学研究。纳米混悬剂的达峰浓度和曲线下面积均显著高于对照制剂, 表明该制剂可显著提高口服吸收。

关键词: 达比加群, 达比加群酯, 液相-质谱/质谱, 纳米混悬剂, 药物动力学

Abstract:

In this study, a sensitive and rapid LC-MS/MS method was developed and validated to determine dabigatran in plasma of beagle dogs after oral administration of dabigatran etexilate nanosuspension (DABE-NS). The analytes (dabigatran) and sertraline hydrochloride (internal standard, IS) were separated on a Kromasil C18 column using gradient elution consisting of methanol and formate buffer at a flow rate of 0.4 mL/min in 20 min. Detection and quantitation were carried out by multiple reaction monitoring following the transitions: m/z 472.17→289.07 and 305.98→275.00 for dabigatran and IS at positive ion mode, respectively. The calibration curves were linear from 1.0 to 500.0  ng/mL for dabigatran with r  = 0.9995. The accuracy of each analyte ranged from 94.8% to 107.1%, and the precision was within 6%. Besides, this method was successfully applied in the investigation of the pharmacokinetic profile of dabigatran in beagle dogs after oral administration ofDABE-NS. The maximum concentration and the areas under curves of dabigatranfor DABE-NS were significantly higher than those of control formulation, indicating improved oral absorption.

Key words: Dabigatran, Dabigatran etexilate, LC-MS/MS, Nanosuspension, Pharmacokinetics

中图分类号: 

Supporting: