The pharmacokinetics of ceftazidime in lactating and non-lactating cows

被引:22
作者
Rule, R
Quiroga, GH
Rubio, M
Buschiazzo, HO
Buschiazzo, PM
机构
[1] COMIS INVEST CIENT PROVINCIA,BUENOS AIRES,DF,ARGENTINA
[2] UNIV BUENOS AIRES,FAC FARM & BIOQUIM,CATEDRA BIODISPONIBILIDAD,RA-1113 BUENOS AIRES,DF,ARGENTINA
关键词
ceftazidime; cephalosporin; cattle; lactation; kinetics; milk;
D O I
10.1007/BF00396297
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The pharmacokinetics of ceftazidime (CAZ) were studied in lactating (LTG) and non-lactating (NLTG) cows. Two groups (LTG and NLTG) of 5 healthy dairy cows were given ceftazidime (10 mg/kg body weight) intravenously (i.v.) and intramuscularly (i.m.). Serum and milk (LTG) and serum samples (NLTG) were collected over a 24-h period post-administration CAZ concentrations in serum and milk were determined by high-performance liquid chromatography, and an interactive and weighted-non-linear least-squares regression analysis was used to perform the pharmacokinetic analysis. The pharmacokinetic profiles in LTG and NLTG cows which had received CAZ i.v. fitted a three-compartment model and a two-compartment model, respectively. The CAZ concentration-time curves in serum and the area under the curve were greater and more sustained (p <0.05) in the LTG cows by both routes, while the serum clearance (Cl-s=72.5+/-18.1 ml/h per kg) was lower (p <0.05) than that in the NLTG cows (Cl-s=185.9+/-44.2 ml/h per kg). CAZ given i.v. exhibited a relatively long half-life of elimination (t(1/2 beta) (LTG)=1.1+/-0.2 h; t(1/2 beta) (NLTG)=1.4+/-0.3 h). Compared with other on cephalosporins, CAZ had good penetration into the mammary gland (47.7+/-38.2% for CAZ i.v.; 51.1+/-1+/-39.0% for CAZ i.m.). Finally, the bioavailability of CAZ (F(LTG)=98.9+/-36.8%;F(NLTG)=77.1+/-25.3%) was suitable for its use by the i.m. route in lactating and non-lactating cows.
引用
收藏
页码:543 / 550
页数:8
相关论文
共 19 条
[1]   BAYESIAN-ANALYSIS OF MINIMUM AIC PROCEDURE [J].
AKAIKE, H .
ANNALS OF THE INSTITUTE OF STATISTICAL MATHEMATICS, 1978, 30 (01) :9-14
[2]  
BAGGOT JD, 1977, PRINCIPLES PHARMACOK
[3]   CLINICAL PHARMACOKINETICS OF THE 3RD GENERATION CEPHALOSPORINS [J].
BALANT, L ;
DAYER, P ;
AUCKENTHALER, R .
CLINICAL PHARMACOKINETICS, 1985, 10 (02) :101-143
[4]   PRINCIPLES OF TISSUE PENETRATION OF ANTIBIOTICS [J].
BARZA, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1981, 8 :7-28
[5]   CEFTAZIDIME LEVELS IN HUMAN-BREAST MILK [J].
BLANCO, JD ;
JORGENSEN, JH ;
CASTANEDA, YS ;
CRAWFORD, SA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1983, 23 (03) :479-480
[6]  
CAPEL EK, 1981, J ANTIMICROBIAL C SB, V8, P241
[7]  
Gibaldi M. P., 1982, PHARMACOKINETICS
[8]  
HARDING SM, 1981, J ANTIMICROBIAL C SB, V7, P263
[9]   CEFTAZIDIME, A PSEUDOMONAS-ACTIVE CEPHALOSPORIN - INVITRO ANTIMICROBIAL ACTIVITY EVALUATION INCLUDING RECOMMENDATIONS FOR DISK DIFFUSION SUSCEPTIBILITY TESTS [J].
JONES, RN ;
BARRY, AL ;
THORNSBERRY, C ;
GERLACH, EH ;
FUCHS, PC ;
GAVAN, TL ;
SOMMERS, HM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1981, 8 :187-211
[10]   COMPARATIVE PHARMACOKINETICS OF YM-13115, CEFTRIAXONE, AND CEFTAZIDIME IN RATS, DOGS, AND RHESUS-MONKEYS [J].
MATSUI, H ;
KOMIYA, M ;
IKEDA, C ;
TACHIBANA, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 26 (02) :204-207