Zhao Bai-Yun, Zhang Jing, Zhao Kai-Yue, Song Yu, Shi Ya-Juan, Zeng Ling, Zeng Xin, Sheng Ying-Gen, Luo Yan
Drug Clinical Trial Institution, Hangzhou Normal University Affiliated Hospital Hangzhou, Zhejiang, China.
Department of Gastroenterology, Affiliated Hospital of Jining Medical University Jining, Shandong, China.
Am J Transl Res. 2024 Sep 15;16(9):5114-5121. doi: 10.62347/WUSG1450. eCollection 2024.
This study aimed to assess the interaction between metoprolol and Ginkgo tablets during their co-administration to provide a reference for clinical prescribing.
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).
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.
Co-administration of metoprolol with Ginkgo tablets resulted in increasing its systemic exposure through inhibiting CYP2D6 activity.
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。
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。
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。
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。