McKenney J M, Swearingen D, Di Spirito M, Doyle R, Pantaleon C, Kling D, Shalwitz R A
National Clinical Reseach Inc, Richmond, Virginia, USA.
J Clin Pharmacol. 2006 Jul;46(7):785-91. doi: 10.1177/0091270006289849.
The coadministration of prescription omega-3-acid ethyl esters (P-OM3) with a statin may present a treatment option for patients with mixed hyperlipidemia. This open-label, randomized, 2-way crossover, drug-drug interaction study evaluated the impact of P-OM3 capsules on plasma simvastatin pharmacokinetics in 24 healthy volunteers. Under fasted conditions, 80 mg simvastatin was administered with or without 4 g P-OM3 for two 14-day periods. After 14 days of dosing to achieve steady state, no significant differences were found in either the extent (AUC(tau)) or rate (Cmax) of exposure to simvastatin or its major beta-hydroxy metabolite after coadministration of P-OM3 with simvastatin compared with administration of simvastatin alone. At steady state, the coadministration of P-OM3 capsules did not appear to affect the pharmacokinetics of simvastatin tablets. The combination of P-OM3 capsules and simvastatin appeared to be well tolerated.
处方用ω-3酸乙酯(P-OM3)与他汀类药物联合使用可能为混合性高脂血症患者提供一种治疗选择。这项开放标签、随机、双向交叉、药物相互作用研究评估了P-OM3胶囊对24名健康志愿者血浆辛伐他汀药代动力学的影响。在禁食条件下,80毫克辛伐他汀在两个14天周期内分别与或不与4克P-OM3一起给药。给药14天达到稳态后,与单独服用辛伐他汀相比,P-OM3与辛伐他汀联合给药后,辛伐他汀及其主要β-羟基代谢产物的暴露程度(AUC(tau))或速率(Cmax)均未发现显著差异。在稳态时,P-OM3胶囊的联合使用似乎不影响辛伐他汀片的药代动力学。P-OM3胶囊与辛伐他汀的组合似乎耐受性良好。