Dietzel K, Beck W S, Schneider H T, Geisslinger G, Brune K
Department of Pharmacology and Toxicology, University of Erlangen-Nuernberg, FRG.
Pharm Res. 1990 Jan;7(1):87-90. doi: 10.1023/a:1015847912059.
The biliary and urinary excretion of ibuprofen and its metabolites were determined in rats after intravenous and peroral administration of 25 and 100 mg/kg of the drug. Within 24 hours 48% of the low i.v. dose and 59% of the high i.v. dose were eliminated via bile as ibuprofen and its metabolites. Following oral administration 40 to 41% of the dose were recovered in bile, whereas 16 to 32% of the dose were eliminated in urine, resulting in an overall drug recovery of 66 to 79% within 24 hours. Upon infusion of bile containing ibuprofen and its metabolites into the duodenum substantial enterohepatic cycling of the drug occurred in the rat.
在大鼠静脉注射和口服25毫克/千克及100毫克/千克布洛芬后,测定了布洛芬及其代谢产物的胆汁和尿液排泄情况。在24小时内,低静脉注射剂量的48%和高静脉注射剂量的59%以布洛芬及其代谢产物的形式通过胆汁排出。口服给药后,40%至41%的剂量在胆汁中回收,而16%至32%的剂量在尿液中排出,24小时内药物总回收率为66%至79%。将含有布洛芬及其代谢产物的胆汁注入十二指肠后,大鼠体内发生了大量药物的肠肝循环。