Conway E L, McNeil J J, Meng L, Drummer O H, Howes L G, Raymond K, Louis W J
University of Melbourne, Clinical Pharmacology and Therapeutics Units, Austin Hospital, Heidelberg, Victoria, Australia.
Clin Pharmacokinet. 1989 Jun;16(6):387-91. doi: 10.2165/00003088-198916060-00004.
The pharmacokinetics of doxazosin were determined in hypertensive subjects after a single dose of 1 mg, and at steady-state while receiving doses of 1, 2, 4 and 8 mg of the drug daily. Chlorothiazide 500 mg once daily was administered as additional therapy throughout the study. After a single dose doxazosin was rapidly absorbed, with peak plasma drug concentrations (Cmax) occurring after 2.1 +/- 0.4 hours. The elimination half-life in plasma was 10.7 +/- 1.2 hours. These parameters remained essentially unchanged during maintenance administration of doxazosin at each of the dose levels. Calculations of Cmax and area under the concentration-time curve (AUC0----infinity) indicated that the pharmacokinetic disposition of the drug remained linear over the dose range 1 to 8 mg.
在高血压患者中测定了多沙唑嗪的药代动力学,单次服用1毫克后以及在每日接受1、2、4和8毫克该药物的稳态情况下进行测定。在整个研究过程中,每日一次给予500毫克氯噻嗪作为辅助治疗。单次服用多沙唑嗪后吸收迅速,血浆药物浓度峰值(Cmax)在2.1±0.4小时后出现。血浆消除半衰期为10.7±1.2小时。在每个剂量水平维持给予多沙唑嗪期间,这些参数基本保持不变。Cmax和浓度-时间曲线下面积(AUC0→∞)的计算表明,在1至8毫克的剂量范围内,该药物的药代动力学处置呈线性。