Chau N P, Zech P Y, Pozet N, Hadj-Aissa A
Clin Pharmacol Ther. 1982 Jun;31(6):770-4. doi: 10.1038/clpt.1982.109.
A 1-mg/kg IV bolus injection and a 150-mg (one tablet) oral dose of ranitidine were given to seven normal subjects. At least 1 wk separated the two doses. Ranitidine disappeared from plasma with a half-life of about 2.5 hr. Half of the oral dose was effectively absorbed and half of the absorbed amount was found unchanged in urine. Total body clearance was 10.1 ml/min/kg. Urinary clearance was the same after oral and intravenous doses (6.4 and 6.9 ml/min/kg, P greater than 0.10). Intravenous ranitidine kinetics included three phases, with a central distribution volume of 0.2 l/kg and a total distribution volume of 1.2 l/kg. Absorption kinetics were apparently order zero: of the 150-mg dose, 75 mg was absorbed during 5 hr at a constant rate of 15 mg/hr.
给7名正常受试者静脉注射1毫克/千克的雷尼替丁大剂量推注,并口服150毫克(1片)雷尼替丁。两次给药至少间隔1周。雷尼替丁从血浆中消失,半衰期约为2.5小时。口服剂量的一半被有效吸收,吸收量的一半在尿液中未发生变化。总体清除率为10.1毫升/分钟/千克。口服和静脉给药后的尿清除率相同(分别为6.4和6.9毫升/分钟/千克,P大于0.10)。静脉注射雷尼替丁的动力学包括三个阶段,中央分布容积为0.2升/千克,总分布容积为1.2升/千克。吸收动力学显然为零级:150毫克剂量中,75毫克在5小时内以15毫克/小时的恒定速率被吸收。