Park Jungsin, Kim Choon Ok, Jin Byung Hak, Yang Seoungwon, Park Min Soo, Hong Taegon
Department of Pharmaceutical Medicine and Regulatory Sciences, Colleges of Medicine and Pharmacy, Yonsei University, Incheon 21983, Republic of Korea.
Departmenrt of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Transl Clin Pharmacol. 2017 Dec;25(4):202-208. doi: 10.12793/tcp.2017.25.4.202. Epub 2017 Dec 20.
Atorvastatin and ezetimibe are frequently co-administered to treat patients with dyslipidemia for the purpose of low-density lipoprotein cholesterol control. However, pharmacokinetic (PK) drug interaction between atorvastatin and ezetimibe has not been evaluated in Korean population. The aim of this study was to investigate PK drug interaction between two drugs in healthy Korean volunteers. An open-label, randomized, multiple-dose, three-treatment, three-period, Williams design crossover study was conducted in 36 healthy male subjects. During each period, the subjects received one of the following three treatments for seven days: atorvastatin 40 mg, ezetimibe 10 mg, or a combination of both. Blood samples were collected up to 96 h after dosing, and PK parameters of atorvastatin, 2-hydroxyatorvastatin, total ezetimibe (free ezetimibe + ezetimibe-glucuronide), and free ezetimibe were estimated by non-compartmental analysis in 32 subjects who completed the study. Geometric mean ratios (GMRs) with 90% confidence intervals (CIs) of the maximum plasma concentration (C) and the area under the curve within a dosing interval at steady state (AUC) of atorvastatin when administered with and without ezetimibe were 1.1087 (0.9799-1.2544) and 1.1154 (1.0079-1.2344), respectively. The corresponding values for total ezetimibe were 1.0005 (0.9227-1.0849) and 1.0176 (0.9465-1.0941). There was no clinically significant change in safety assessment related to either atorvastatin or ezetimibe. Co-administration of atorvastatin and ezetimibe showed similar PK and safety profile compared with each drug alone. The PK interaction between two drugs was not clinically significant in healthy Korean volunteers.
阿托伐他汀和依折麦布经常联合使用,以治疗血脂异常患者,目的是控制低密度脂蛋白胆固醇。然而,阿托伐他汀和依折麦布之间的药代动力学(PK)药物相互作用尚未在韩国人群中进行评估。本研究的目的是调查这两种药物在健康韩国志愿者中的PK药物相互作用。对36名健康男性受试者进行了一项开放标签、随机、多剂量、三治疗、三周期、威廉姆斯设计的交叉研究。在每个周期中,受试者接受以下三种治疗之一,为期7天:阿托伐他汀40毫克、依折麦布10毫克或两者联合使用。给药后长达96小时采集血样,并通过非房室分析对32名完成研究的受试者估计阿托伐他汀、2-羟基阿托伐他汀、总依折麦布(游离依折麦布+依折麦布-葡萄糖醛酸苷)和游离依折麦布的PK参数。阿托伐他汀在联合使用和不使用依折麦布时,最大血浆浓度(C)和稳态给药间隔内曲线下面积(AUC)的几何平均比值(GMRs)及其90%置信区间(CIs)分别为1.1087(0.9799-1.2544)和1.1154(1.0079-1.2344)。总依折麦布的相应值为1.0005(0.9227-1.0849)和1.0176(0.9465-1.0941)。与阿托伐他汀或依折麦布相关的安全性评估没有临床显著变化。与单独使用每种药物相比,阿托伐他汀和依折麦布联合使用显示出相似的PK和安全性特征。在健康韩国志愿者中,两种药物之间的PK相互作用没有临床意义。