Achari R, Hulse J D, Drissel D, Matier W L
Br J Clin Pharmacol. 1985 Dec;20(6):691-4. doi: 10.1111/j.1365-2125.1985.tb05131.x.
The steady state pharmacokinetics of flestolol, a short acting beta-adrenoceptor blocking agent, were studied in six healthy subjects following intravenous infusion of six different doses; 18, 24, 35, 50, 75 and 100 micrograms kg-1 min-1, for 60 min. Steady state blood levels increased linearly with dose for all six subjects. The overall mean half-life was 6.5 min. The total body clearance averaged 208 ml min-1 kg-1 indicating significant extrahepatic metabolism of the drug. There were no significant changes in the half-lives or the total body clearances after the six doses, suggesting that the kinetics of flestolol are linear over the dose range studied.
在六名健康受试者中,静脉输注六种不同剂量(18、24、35、50、75和100微克/千克/分钟)的短效β-肾上腺素能受体阻滞剂氟司洛尔60分钟后,对其稳态药代动力学进行了研究。所有六名受试者的稳态血药浓度均随剂量呈线性增加。总体平均半衰期为6.5分钟。总体清除率平均为208毫升/分钟/千克,表明该药物有显著的肝外代谢。六种剂量后半衰期和总体清除率均无显著变化,提示在所研究的剂量范围内氟司洛尔的动力学呈线性。