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作 者:刘文芳[1] 杨克旭[1] 荆珊[1] 杜海燕[1] 林阳[1] Meihua Rose FENG LIU Wen-fang;YANG Ke-xu;JING Shan;DU Hai-yan;LIN Yang;Meihua Rose FENG(Institute of Clinical Pharmacology,Anzhen Hospital of Capital Medical University,Beijing 100029,China;College of Pharmacy,University of Michigan,Ann Arbor 48109,MI,American)
机构地区:[1]首都医科大学附属北京安贞医院临床药理中心,北京100029 [2]美国密歇根大学药学院,美国密歇根州安娜堡48109
出 处:《中国临床药理学杂志》2020年第10期1353-1356,共4页The Chinese Journal of Clinical Pharmacology
基 金:“十三五”新药创制重大专项基金资助项目(2017ZX09304017)。
摘 要:目的建立中国健康受试者单剂量口服阿雷地平的群体药代动力学模型,探索剂量比例性,为临床合理用药提供依据。方法将47例健康中国受试者分为3个剂量组,分别单剂量口服阿雷地平肠溶胶囊5 mg (n=12)、10 mg (n=23)和20 mg(n=12),用非线性混合效应模型(NONMEM)建立群体药代动力学模型,并探讨剂量比例性。结果血浆中阿雷地平血药浓度时间曲线符合二室模型,吸收速率常数、表观清除率、中央室和外周室的分布容积群体典型值分别为0.608/h,748 L·h^-1,211 L和740 L。5,10和20 mg剂量下,阿雷地平体内暴露随着剂量增加成比例增加。结论本研究的阿雷地平群体药代动力学模型稳定、可靠,可以作为阿雷地平个体化治疗的依据。Objective To characterize aranidipine population pharmacokinetics and dose proportionality in Chinese subjects, to support the proper dosing in Chinese patients. Methods Forty-seven Chinese healthy subjects were enrolled and assigned to take a single oral dose of 5 mg(n=12), 10 mg(n=23), and 20 mg(n=12) aranidipine capsules. Population pharmacokinetic(POPPK) modeling was performed using nonlinear mixed effects modeling(NONMEM), and dose proportionality was investigated. Results Plasma aranidipine concentration-time profiles under fasted state were best described by a two-compartment PK model with first-order absorption. The pharmacokinetic parameters in Chinese healthy subjects were well estimated. Aranidipine absorption rate constant(Ka), apparent clearance(CL/F), volume of distribution in the central compartments(V2/F) and peripheral compartments(V3/F) were 0.608/h, 748 L·h^-1, 211 L and 740 L respectively. AR exposure, expressed in AUC0-t and Cmax, was proportionally increased with dose over the dose range of 5, 10 and 20 mg. Conclusion The POPPK model developed in the present study could provide very useful information for dose optimization and individualization in Chinese patients.
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