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首页> 外文期刊>European journal of drug metabolism and pharmacokinetics >Mefloquine pharmacokinetics in healthy subjects and in peptic ulcer patients after cimetidine administration.
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Mefloquine pharmacokinetics in healthy subjects and in peptic ulcer patients after cimetidine administration.

机译:西咪替丁用药后在健康受试者和消化性溃疡患者中的甲氟喹药代动力学。

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The pharmacokinetics of orally administered mefloquine were determined in six healthy male subjects and in six ulcer patients before and after a 3-day course of cimetidine (400 mg morning and evening). Peak plasma concentrations Cmax and AUC0-infinity were similarly and significantly (P < 0.05) increased after cimetidine pretreatement in both healthy subjects and peptic ulcer patients Cmax was increased by 42.4% and 20.5% while AUC0-infinity was increased by 37.5% in healthy and peptic ulcer subjects respectively. The values of t1/2ab absorption and t1/2 beta elimination, total crearance CLT/F and volume of distribution were altered to varying levels after cimetidine treatment but the changes were not statistically significant in both healthy and peptic ulcer subjects. The established long t1/2 beta and this apparent interaction between mefloquine and cimetidine which resulted in increased mefloquine plasma concentration might be of clinical significant in patients with neurological/psychiatric history.
机译:西咪替丁3天疗程(400 mg早晚)之前和之后,在6名健康男性受试者和6名溃疡患者中确定了口服甲氟喹的药代动力学。西咪替丁预处理后,健康受试者和消化性溃疡患者的血浆峰值浓度Cmax和AUC0-infinity相似且显着增加(P <0.05),健康人和消化性溃疡患者中Cmax分别增加42.4%和20.5%,而AUC0-infinity则增加37.5%。消化性溃疡分别。西咪替丁治疗后,t1 / 2ab吸收和t1 / 2β消除,总清除率CLT / F和分布体积的值更改为不同水平,但在健康和消化性溃疡受试者中,变化均无统计学意义。建立的较长的t1 / 2 beta以及甲氟喹和西咪替丁之间这种明显的相互作用导致甲氟喹的血浆浓度升高,在具有神经/精神病史的患者中可能具有临床意义。

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