Hildebrand M, Krause W, Oberender H A, Zurdel-Dillinger S, Jünger M, Bodenburg H
Research Laboratories Schering AG, Berlin.
Eicosanoids. 1990;3(3):145-8.
The pharmacokinetics of iloprost were studied in 12 hospitalized patients suffering from severe peripheral arterial occlusive disease (PAOD) stages III or IV according to Fontaine. The patients were 8 males and 4 females aged from 49 to 83 years. Apart from PAOD, several other concomitant diseases were present, e.g. myocardial and/or renal insufficiency, diabetes and hypertension. Patients were treated daily with i.v. infusions of iloprost at dosages of 1.0-3.3 ng/kg/min over a period of 4 to 6 h. Dose-normalized steady-state plasma levels ranged from 39 to 100 pg/ml (65 +/- 20 pg/ml). The total clearance accounted for 16 +/- 5 ml/min/kg. Post-infusion disposition in the plasma was biphasic with half-lives of 4 +/- 2 min and 37 +/- 8 min. The plasma level profiles obtained on days 4 and 14 of treatment in 3 patients were similar. Sex specific kinetic differences were not observed. In comparison to healthy volunteers, studied in an earlier trial, total clearance was slightly lower and consequently steady state levels were increased (p less than 0.05) in PAOD patients. Half-lives in the plasma were not significantly different.
依洛前列素的药代动力学在12例根据Fontaine分级处于III或IV期的重度外周动脉闭塞性疾病(PAOD)住院患者中进行了研究。患者年龄在49至83岁之间,其中8例为男性,4例为女性。除PAOD外,还存在其他几种伴随疾病,如心肌和/或肾功能不全、糖尿病和高血压。患者每天接受静脉输注依洛前列素治疗,剂量为1.0 - 3.3 ng/kg/min,持续4至6小时。剂量标准化稳态血浆水平范围为39至100 pg/ml(65±20 pg/ml)。总清除率为16±5 ml/min/kg。输注后血浆中的药物处置呈双相,半衰期分别为4±2分钟和37±8分钟。3例患者在治疗第4天和第14天获得的血浆水平曲线相似。未观察到性别特异性动力学差异。与早期试验中研究的健康志愿者相比,PAOD患者的总清除率略低,因此稳态水平升高(p<0.05)。血浆半衰期无显著差异。