The aim of this work was to determine the pharmacokinetics of intravenous (iv) and intramuscular (im) ceftazidime administered to lactating (LTG; n = 6) and non-lactating (NLTG; n=6) healthy Creole goats in 2 trials (T1 and T2). During T1 and T2, goats randomly received a single dose of im or iv ceftazidime (10 mg/kg). Serum concentration of iv ceftazidime in NLTG and LTG goats is best described by 2 and 3 compartment models, respectively. The pharmacokinetic parameters of iv and im ceftazidime administered to LTG and NLTG showed statistically significant differences (P<0.05) in the constants (λz, T1 vs T2 [iv] 0.5±0.1 vs 0.3±0.1 /h; T1 vs T2 [im] 0.5±0.2 vs 0.3±0.1 /h) and in the mean times (t1/2, T 1 vs T 2 [iv] 1.6±0.3 vs 2.3±0.6 h; T 1 vs T 2 [im] 1.6±0.7 vs 2.6±0.9 h) of elimination. The bioavailability of ceftazidime in LTG and NLTG was 113.0 ± 17.8 and 96.0 ± 18.0 %, respectively. Ceftazidime concentration in milk at 2 h was: iv = 1.9 ± 0.2 and im = 2.4 ± 0.5 μg/m ; the penetration in milk was iv = 18.3 ± 13.5 and im = 14.3 ± 10.6 %. Ninety-six hours after iv and im administration, residues of the drug were not found in milk. In conclusion, ceftazidime, when administered to goats, showed high concentration times in serum, good penetration into milk and a bioavailability that makes it suitable to be used by the im route
CEFOTAXIME and ceftazidime are third-generation cephalosporins that are stable to 3-lactamases and have a wide antibacterial spectrum and low toxicity (O'
ABSTRACT:The aim of the present study was to correlate the milk production and the kinetic variables in milk of cephalothin administered to goats. Twenty healthy creole goats in milk production were used. Cephalothin was administered by intravenous route (20 mg/kg b.w.). Milk samples were collected at 0.25, 0.5, 1.0, 2.0, 3.0, 4.0, 5.0, 6.0, 8.0 and 12.0 hours postadministration of the antibiotic. Cephalothin concentrations were measured in milk samples by high performance liquid chromatography. The values (mean ± standard error) of milk production collected during 24 hours previous to the administration of the antibiotic were 761.5 ± 111.1 ml. The results of the kinetic variables (mean ± standard error) of cephalothin in milk were: AUC = 5.4 ± 1.6 µg/ml/h; C max = 1.1 ± 0.3 µg/ml and t max = 1.7 ± 0.1 h. The correlation coefficients AUC-milk production, C max -milk production and t max -milk production were: 0.602 (P < 0.01), 0.596 (P < 0.01) and 0.398 (P < 0.1), respectively. In conclusion, the areas under the curve and the maximum concentrations and the time to reach them in milk are in fact related to the volume of milk produced by the goats.
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