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苯磺酸白芍总苷对大鼠体内来氟米特药代动力学、排泄及组织分布的影响。

Effects of paeoniflorin-6'-O-benzene sulfonate on the pharmacokinetics, excretion and tissue distribution of leflunomide in rats.

机构信息

Institute of Clinical Pharmacology, Key Laboratory of Anti-inflammatory and Immune Medicine, Ministry of Education, Anti-inflammatory Immune Drugs Collaborative Innovation Center, Anhui Medical University, Hefei, China.

出版信息

Basic Clin Pharmacol Toxicol. 2022 Mar;130(3):364-374. doi: 10.1111/bcpt.13685. Epub 2021 Dec 27.

Abstract

Paeoniflorin-6'-O-benzene sulfonate (CP-25) is a novel ester derivative of paeoniflorin, which has been shown to have synergistic pharmacodynamic effects with leflunomide (LEF). To determine the effects of CP-25 on the pharmacokinetics of LEF in rats, we developed a ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)-based method for the determination of levels of teriflunomide (TER, an active metabolite of LEF). This method was used to determine TER concentrations in the plasma, urine, faeces and bile; heart, liver, spleen, lung, kidney, intestinal, brain and synovial tissues; and peripheral blood mononuclear cells (PBMCs) of rats in the control (LEF [10 mg/kg]) and combined (CP-25 [50 mg/kg × 7d] plus LEF [10 mg/kg]) groups. TER area under the curve [AUC], T , mean residence time (MRT), t and t were significantly lower, and clearance (CL) was significantly higher in the combined group than in the control group. Oral CP-25 administration in combination with LEF was found to promote TER excretion in urine, faeces and bile and to reduce its contents in most tissues and organs, especially in the liver, which may reduce LEF-induced liver injury. CP-25 also increased TER exposure in the synovium and its absorption by PBMCs, and this could explain the synergistic effects of CP-25 and LEF.

摘要

苯磺酸白芍苷(CP-25)是白芍苷的一种新型酯衍生物,已显示与来氟米特(LEF)具有协同药效作用。为了确定 CP-25 对大鼠 LEF 药代动力学的影响,我们开发了一种基于超高效液相色谱-串联质谱(UPLC-MS/MS)的方法来测定来氟米特(LEF 的活性代谢物)的浓度。该方法用于测定对照组(LEF[10mg/kg])和联合组(CP-25[50mg/kg×7d]加 LEF[10mg/kg])大鼠血浆、尿液、粪便、胆汁、心脏、肝脏、脾脏、肺脏、肾脏、肠、脑和滑膜组织以及外周血单核细胞(PBMCs)中 TER 的浓度。与对照组相比,联合组 TER 的曲线下面积(AUC)、T 、平均驻留时间(MRT)、t 和 t 显著降低,清除率(CL)显著升高。口服 CP-25 联合 LEF 可促进 TER 在尿液、粪便和胆汁中的排泄,并降低其在大多数组织和器官中的含量,尤其是在肝脏中,这可能降低 LEF 引起的肝损伤。CP-25 还增加了 TER 在滑膜中的暴露和 PBMCs 的吸收,这可以解释 CP-25 和 LEF 的协同作用。

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