van Agtmael M A, Gupta V, van der Wösten T H, Rutten J P, van Boxtel C J
Department of Clinical Pharmacology and Pharmacotherapy, Amsterdam, The Netherlands.
Eur J Clin Pharmacol. 1999 Jul;55(5):405-10. doi: 10.1007/s002280050648.
To evaluate the effect of grapefruit juice on the pharmacokinetics of artemether in plasma and saliva after a single oral dose and to detect concentration-dependent electrocardiographic changes (bradycardia and QTc prolongation).
Six healthy male subjects were given a standard breakfast followed by two tablets of 50-mg artemether administered with water; 1 week later, the tablets were administered with 350 ml double-strength fresh frozen grapefruit juice. For 8 h, 17 blood- and saliva samples were collected, and 17 electrocardiograms were recorded. Drug and metabolite concentrations were measured by means of high-performance liquid chromatography with electrochemical detection. The pharmacokinetic parameters were determined using a one-compartment model.
Grapefruit juice significantly (P = 0.001) increased the mean peak concentration (Cmax) of artemether more then twofold from 42 (SD 17) ng/ml to 107 (28) ng/ml. The time to reach Cmax (tmax) with grapefruit juice was 2.1 (0.6) h compared with 3.6 (17) h with water (P = 0.02). The area under the concentration time curve (AUC) almost doubled with grapefruit juice from 177 ng x h/ml to 336 ng x h/ml (P = 0.003). The elimination half-life remained unchanged (1.0 h vs 1.3 h). No major changes in the kinetics of the metabolite dihydroartemisinin were detected. Low artemether levels and zero dihydroartemisinin levels were found in saliva. No influences of artemether were observed on 17 electrocardiograms during the 8 h after drug intake in particular there were no signs of bradycardia or QTc prolongation.
Grapefruit juice significantly increases the oral bioavailability of artemether without an effect on the elimination half-life. It suggests a role for intestinal CYP3A4 in the presystemic metabolism of artemether.
评估单次口服剂量后葡萄柚汁对蒿甲醚血浆和唾液药代动力学的影响,并检测浓度依赖性心电图变化(心动过缓和QTc延长)。
6名健康男性受试者先食用标准早餐,然后用水送服两片50毫克的蒿甲醚片剂;1周后,用350毫升双倍浓度的新鲜冷冻葡萄柚汁送服片剂。在8小时内,采集17份血液和唾液样本,并记录17份心电图。采用高效液相色谱电化学检测法测定药物和代谢物浓度。使用单室模型确定药代动力学参数。
葡萄柚汁显著(P = 0.001)提高了蒿甲醚的平均峰浓度(Cmax),使其从42(标准差17)纳克/毫升增加到107(28)纳克/毫升,增幅超过两倍。饮用葡萄柚汁时达到Cmax的时间(tmax)为2.1(0.6)小时,而用水送服时为3.6(1.7)小时(P = 0.02)。饮用葡萄柚汁后,浓度-时间曲线下面积(AUC)几乎翻倍,从177纳克·小时/毫升增至336纳克·小时/毫升(P = 0.003)。消除半衰期保持不变(1.0小时对1.3小时)。未检测到代谢物双氢青蒿素动力学的重大变化。唾液中蒿甲醚水平较低,双氢青蒿素水平为零。在服药后8小时内,未观察到蒿甲醚对17份心电图有影响,尤其没有心动过缓或QTc延长的迹象。
葡萄柚汁显著提高了蒿甲醚的口服生物利用度,且对消除半衰期无影响。这表明肠道CYP3A4在蒿甲醚的首过代谢中起作用。