Chau N P, Flouvat B L, Le Roux E, Safar M E
Clin Pharmacol Ther. 1980 Jul;28(1):6-11. doi: 10.1038/clpt.1980.123.
Prazosin kinetics were studied in 8 hypertensive patients (4 male and 4 female) with normal renal function. Intravenous data showed a 3-phase distribution. As a result, a linear 3-compartment model with elimination from the central compartment was proposed to describe the drug kinetics. Prazosin disappeared from plasma with a terminal half-life t1/2 of about 3 hr and had a central distribution volume of about 0.18 1/kg. Only a negligible fraction of the dose was found unchanged in urine. The oral data showed that, of the 2-mg dose, about 1 mg was effectively absorbed. This fraction was almost entirely absorbed in 2 hr. Absorption kinetics were apparently linear with a t1/2 of about 30 min.
在8名肾功能正常的高血压患者(4名男性和4名女性)中研究了哌唑嗪的动力学。静脉给药数据显示为三相分布。因此,提出了一个从中央室消除的线性三室模型来描述药物动力学。哌唑嗪从血浆中消失,终末半衰期t1/2约为3小时,中央分布容积约为0.18升/千克。在尿液中发现未变化的剂量仅占可忽略不计的一小部分。口服给药数据显示,2毫克剂量中约1毫克被有效吸收。这部分几乎在2小时内完全吸收。吸收动力学明显呈线性,t1/2约为30分钟。