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银杏叶片对大鼠美托洛尔药代动力学的影响:基于液相色谱-串联质谱法的研究

Effect of Ginkgo tablets on the pharmacokinetics of metoprolol in rats: liquid chromatography-tandem mass spectrometry-based study.

作者信息

Zhao Bai-Yun, Zhang Jing, Zhao Kai-Yue, Song Yu, Shi Ya-Juan, Zeng Ling, Zeng Xin, Sheng Ying-Gen, Luo Yan

机构信息

Drug Clinical Trial Institution, Hangzhou Normal University Affiliated Hospital Hangzhou, Zhejiang, China.

Department of Gastroenterology, Affiliated Hospital of Jining Medical University Jining, Shandong, China.

出版信息

Am J Transl Res. 2024 Sep 15;16(9):5114-5121. doi: 10.62347/WUSG1450. eCollection 2024.

Abstract

OBJECTIVES

This study aimed to assess the interaction between metoprolol and Ginkgo tablets during their co-administration to provide a reference for clinical prescribing.

METHODS

The co-administration of metoprolol (20 mg/kg) and Ginkgo tablets (2.4 mg/kg) was conducted in adult Sprague Dawley (SD) rats (n = 8). An optimized liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the analysis of plasma metoprolol to evaluate its pharmacokinetics. , the rat liver microsomes were employed to assess the effect of Ginkgo tablets on the metabolic stability of metoprolol and the activity of Cytochrome P450 2D6 (CYP2D6).

RESULTS

The developed LC-MS/MS method was demonstrated of high sensitivity, accuracy, and precision. When co-administered with Ginkgo tablets, it increased the area under the curve (AUC, 59.01 ± 10.11 39.19 ± 10.21 μg/mL × min), the maximum plasma concentration (C, 461.72 ± 44.64 276.35 ± 118.09 ng/mL), and the half-life (t, 302.83 ± 91.52 262.34 ± 111.12 min) of metoprolol in rats and reduced the clearance rate (0.346 ± 0.057 0.539 ± 0.145 L/min/kg). , Ginkgo tablets improved the metabolic stability of metoprolol and suppressed the activity of CYP2D6 in a concentration-dependent manner with the IC value of 11.17 μM.

CONCLUSION

Co-administration of metoprolol with Ginkgo tablets resulted in increasing its systemic exposure through inhibiting CYP2D6 activity.

摘要

目的

本研究旨在评估美托洛尔与银杏片合用时的相互作用,为临床用药提供参考。

方法

将美托洛尔(20 mg/kg)与银杏片(2.4 mg/kg)联合给予成年Sprague Dawley(SD)大鼠(n = 8)。建立了一种优化的液相色谱-串联质谱(LC-MS/MS)方法用于分析血浆中美托洛尔,以评估其药代动力学。此外,采用大鼠肝微粒体评估银杏片对美托洛尔代谢稳定性及细胞色素P450 2D6(CYP2D6)活性的影响。

结果

所建立的LC-MS/MS方法具有高灵敏度、准确性和精密度。与银杏片合用时,美托洛尔在大鼠体内的曲线下面积(AUC,59.01±10.11比39.19±10.21μg/mL×min)、最大血浆浓度(Cmax,461.72±44.64比276.35±118.09 ng/mL)和半衰期(t1/2,302.83±91.52比262.34±111.12 min)增加,清除率降低(0.346±0.057比0.539±0.145 L/min/kg)。此外,银杏片以浓度依赖性方式提高了美托洛尔的代谢稳定性并抑制了CYP2D6的活性,IC50值为11.17μM。

结论

美托洛尔与银杏片合用通过抑制CYP2D6活性导致其全身暴露增加。

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