Pharmacokinetics of azithromycin after i.v. and i.m. administration to sheep

被引:11
|
作者
Cárceles, CM [1 ]
Font, A [1 ]
Escudero, E [1 ]
Espuny, A [1 ]
Marín, P [1 ]
Fernández-Varón, E [1 ]
机构
[1] Univ Murcia, Fac Vet Med, Dept Pharmacol, E-30071 Murcia, Spain
关键词
D O I
10.1111/j.1365-2885.2005.00680.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacokinetics (PK) of azithromycin after i.v. and i.m. injection at a single dosage of 20 mg/kg bodyweight was studied in sheep. Blood samples were collected from the jugular vein until 120 h after dosing for both routes. Plasma concentrations of azithromycin were determined by bioassay. The plasma concentration-time data of azithromycin best fitted a three-compartment model after i.v. administration and a two-compartment model with first-order absorption after i.m. administration. The elimination half-life (t(1/2 lambda z)) was 47.70 +/- 7.49 h after i.v. administration and 61.29 +/- 13.86 h after i.m. administration. Clearance value after i.v. dosing was 0.52 +/- 0.08 L/kg.h. After i.m. administration a peak azithromycin concentration (C-max) of 1.26 +/- 0.19 mg/L was achieved at 1.24 +/- 0.31 h (t(max)). Area under the curve (AUC) were 38.85 +/- 5.83 mg.h/L and 36.03 +/- 1.52 mg.h/L after i.v. and i.m. administration respectively. Bioavailability obtained after i.m. administration was 94.08 +/- 11.56%. The high tolerability of this i.m. preparation and the favourable PK behaviour such as the long half-life and high bioavailability make azithromycin likely to be effective in sheep.
引用
收藏
页码:475 / 479
页数:5
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