Nawaz M, Hafeez M, Khan F H, Nawaz R, Iqbal T
Zentralbl Veterinarmed A. 1989 Feb;36(2):84-9. doi: 10.1111/j.1439-0442.1989.tb00707.x.
Bioavailability, disposition kinetics and renal clearance of ampicillin were investigated in 8 sheep following intravenous (i.v.), or intramuscular (i.m.) injection of 10 mg/kg or oral administration of 20 mg/kg dose. Peak of absorption was achieved in 26 +/- 9 min (mean +/- SD) after i.m. and 85 +/- 24 min after oral administration. The relative bioavailability of i.m. injected drug was 95 +/- 20 per cent compared to only 37 +/- 7 per cent following oral administration of double the dose. The disposition kinetics parameters of ampicillin were comparable in sheep with all three routes of drug administration. The renal clearance of ampicillin varied between 0.20 and 0.62 ml/min.kg while total body clearance was 50 to 64 ml/min.kg. The fractional urinary excretion of ampicillin in the first 8 hours after dosing was less than 1 per cent of the dose by all three routes.
在8只绵羊中,静脉注射(i.v.)、肌肉注射(i.m.)10mg/kg或口服20mg/kg剂量后,研究了氨苄西林的生物利用度、处置动力学和肾清除率。肌肉注射后26±9分钟(平均值±标准差)和口服给药后85±24分钟达到吸收峰值。肌肉注射药物的相对生物利用度为95±20%,而口服双倍剂量后仅为37±7%。氨苄西林的处置动力学参数在绵羊的三种给药途径中具有可比性。氨苄西林的肾清除率在0.20至0.62ml/min.kg之间,而全身清除率为50至64ml/min.kg。给药后前8小时,氨苄西林经三种途径的尿排泄分数均小于给药剂量的1%。