Cook Chyung S, Zhang Liming
Global Drug Metabolism, Pharmacia Corporation, 4901 Searle Parkway, Skokie, Illinois 60077, USA.
J Pharm Sci. 2002 Mar;91(3):607-14. doi: 10.1002/jps.10053.
This study was conducted to investigate why a food effect was observed following an intravenous dose of eplerenone (EP) in the dog, but not following oral dosing. Three female dogs were implanted with a chronic portal vein access port and received radiolabeled EP doses orally (15 mg/kg in solution) and intravenously (7.5 mg/kg via cephalic and portal veins) under fasted and fed conditions. Mean AUC values for EP after infusion through the cephalic vein were 23.0 +/- 2.7 and 18.2 +/- 1.1 h.microg/mL under fasted and fed conditions, respectively. Corresponding values after infusion through the portal vein were 20.7 +/- 3.2 and 12.9 +/- 1.3 h.microg/mL, respectively. After oral administration, EP was absorbed 82.0 +/- 6.9 and 98.0 +/- 8.3% under fasted and fed conditions; corresponding mean AUC values were 32.0 +/- 2.0 and 30.8 +/- 3.6 h.microg/mL, respectively. The AUC value for SC-70303 acid (the open lactone form of EP) was lower under fed conditions after cephalic vein infusion, but was greater under fed conditions after portal vein infusion or oral solution administration. The hepatic first-pass effect of EP was 12.6 +/- 6.3% under fasted conditions and 27.1 +/- 6.0% under fed conditions. Pharmacokinetic analysis of EP concentrations after portal vein infusion and oral administration showed that under fed conditions the rate constants for bile excretion and for liver metabolism and urinary excretion were increased while the rate constant for elimination and/or metabolism in the gastrointestinal tract was reduced. In conclusion, the apparent lack of food effect after oral administration was observed because enhanced clearance was compensated by increased absorption.
本研究旨在探究为何静脉注射依普利酮(EP)后在犬体内观察到食物效应,而口服给药后却未观察到。三只雌性犬植入慢性门静脉接入端口,在禁食和进食条件下分别口服(溶液中15mg/kg)和静脉注射(通过头静脉和门静脉7.5mg/kg)放射性标记的EP剂量。通过头静脉输注后,禁食和进食条件下EP的平均AUC值分别为23.0±2.7和18.2±1.1h·μg/mL。通过门静脉输注后的相应值分别为20.7±3.2和12.9±1.3h·μg/mL。口服给药后,禁食和进食条件下EP的吸收分别为82.0±6.9%和98.0±8.3%;相应的平均AUC值分别为32.0±2.0和30.8±3.6h·μg/mL。头静脉输注后,进食条件下SC - 70303酸(EP的开环内酯形式)的AUC值较低,但门静脉输注或口服溶液给药后进食条件下的AUC值较高。禁食条件下EP的肝首过效应为12.6±6.3%,进食条件下为27.1±6.0%。门静脉输注和口服给药后EP浓度的药代动力学分析表明,进食条件下胆汁排泄、肝脏代谢和尿排泄的速率常数增加,而胃肠道消除和/或代谢的速率常数降低。总之,口服给药后未观察到明显的食物效应,是因为清除率的提高被吸收增加所补偿。