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中国药学(英文版) ›› 2017, Vol. 26 ›› Issue (10): 747-753.DOI: 10.5246/jcps.2017.10.084

• 【研究论文】 • 上一篇    下一篇

UPLC-MS-MS法测定大鼠血浆中8,2′-二异戊烯基槲皮素-3-甲醚的浓度及其药物动力学研究

刘焕, 范珊珊, 张雯, 张驿帆, 李腾, 尚明英*, 刘广学, 徐风, 蔡少青   

  1. 北京大学医学部 药学院 天然药物学系, 北京 100191
  • 收稿日期:2017-08-27 修回日期:2017-09-25 出版日期:2017-10-31 发布日期:2017-10-12
  • 通讯作者: Tel.: +86-010-82802534, E-mail: myshang@bjmu.edu.cn
  • 基金资助:

    National Natural Science Foundation of China (Grant No. 81673590) and National Key Technology R&D Program “New Drug Innovation” of China (Grant No. 2013ZX09103002-006).

Determination of 8,2′-diprenylquercetin 3-methyl ether in plasma by UPLC-MS-MS and its pharmacokinetic application in rats

Huan Liu, Shanshan Fan, Wen Zhang, Yifan Zhang, Teng Li, Mingying Shang*, Guangxue Liu, Feng Xu, Shaoqing Cai   

  1. Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
  • Received:2017-08-27 Revised:2017-09-25 Online:2017-10-31 Published:2017-10-12
  • Contact: Tel.: +86-010-82802534, E-mail: myshang@bjmu.edu.cn
  • Supported by:

    National Natural Science Foundation of China (Grant No. 81673590) and National Key Technology R&D Program “New Drug Innovation” of China (Grant No. 2013ZX09103002-006).

摘要:

8,2′-二异戊烯基槲皮素-3-甲醚是藏药小叶莲中的主要成分,具有较好的抗乳腺癌活性。本文首次建立了快速、灵敏的测定大鼠血浆中8,2′-二异戊烯基槲皮素-3-甲醚浓度的UPLC-MS/MS方法。以8-异戊烯基山柰酚为内标,采用waters ACQUITY UPLC BEH C18色谱柱(2.1 mm×100 mm, 1.7μm),0.1%甲酸水乙腈为流动相梯度洗脱,流速为0.4 mL·min1, 柱温30 ºC。通过电喷雾离子化四极杆串联质谱,负离子多反应监测(MRM)模式,用于定量分析的离子反应分别为m/z 451.30→177.25 (8,2′-二异戊烯基槲皮素-3-甲醚)m/z 353.25→298.15 (8-异戊烯基山柰酚)8,2′-二异戊烯基槲皮素-3-甲醚浓度为0.1–2000 ng/mL时线性关系良好(r = 0.9954), 高、中、低三个浓度的提取回收率在103%–115%范围内,日内、日间精密度均小于15%,准确度在–6%~15%之间。该方法简单快速灵敏,适用于检测8,2′-二异戊烯基槲皮素-3-甲醚的血药浓度并进行大鼠体内的药动力学研究。药物动力学试验结果表明,雌性大鼠口服灌胃给药100 mg/kg8,2′-二异戊烯基槲皮-3-甲醚, 2小时达到血浆峰浓度,生物半衰期为6.79小时, 20小时内能维持一定量的血药浓度,有利于药物在生物体内产生作用。

关键词: 8,2'-二异戊烯基槲皮素-3-甲醚, 超高效液相串联质谱, 血药浓度, 抗乳腺癌, 药物动力学

Abstract:

8,2′-Diprenylquercetin 3-methyl ether with significant anti-breast cancer activityis the main constituent of Tibetan medicine Sinopodophylli Fructus. In the present study, we developed and validated a rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of 8,2′-diprenylquercetin 3-methyl etherin rat plasma. 8-Prenylkaempferol was used as the internal standard. The separation was carried out using Waters ACQUITY UPLC BEH C18 column (2.1 mm×100 mm, 1.7 µm) with a mobile phase consisting of acetonitrile and 0.1% formic acid in water on a gradient program at a flow rate of 0.4 mL·min–1 and temperature of 30 ºC. Triple quadrupole mass spectrometric detection in negative ion mode was used for multiple-reaction monitoring of the transitions at m/z 451.30→177.25 and m/z 353.25→298.15 for 8,2′-diprenylquercetin 3-methyl ether and 8-prenylkaempferol, respectively. The calibration curves were linear within the concentration range 0.1–2000 ng/mL (r = 0.9954). The recoveries were 103%–115%, and the results were consistent across low, middle and high concentration levels. The intra- and inter-day precisions were within 15%, and the bias was between –6%~15%. This method was simple, rapid and sensitive, which could be applied to the determination of 8,2′-diprenylquercetin 3-methyl ether in plasma and pharmacokinetic study in rats. Pharmacokinetic test indicated that the peak plasma concentration occurred in 2 h after the female rats were intragastrically administered with 8,2′-diprenylquercetin 3-methyl ether at the dose of 100 mg/kg, and the biological half-life was 6.79 h. The blood drug concentration maintained equal amount for 20 h, which was conducive to the in vivo effects of drugs.

Key words: 8,2'-Diprenylquercetin 3-methyl ether, UPLC-MS/MS, Blood concentration, Anti-breast cancer, Pharmacokinetic

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