Wilson W D, Spensley M S, Baggot J D, Hietala S K, Pryor P
Department of Medicine, School of Veterinary Medicine, University of California, Davis 95616.
J Vet Pharmacol Ther. 1991 Mar;14(1):78-89. doi: 10.1111/j.1365-2885.1991.tb00807.x.
The pharmacokinetics and bioavailability of ticarcillin and clavulanate were determined after intravenous (i.v.) or intramuscular (i.m.) administration of ticarcillin disodium (50 mg/kg) combined with clavulanate potassium (1.67 mg/kg) to groups of healthy foals at 3 days and 28 days of age. After i.v. administration of the combination to five foals, the disposition kinetics of ticarcillin and clavulanate were best described using a two-compartment open model. Mean plasma elimination-rate constant (beta) and clearance (ClB) for ticarcillin were significantly less (P less than 0.01), and volume of distribution at steady state (Vd(ss)) was significantly larger (P less than 0.05), in the foals at 3 days compared with 28 days of age. This indicated that renal excretion mechanisms were immature and ticarcillin was more widely distributed in 3-day-old foals. The mean elimination rate constant for clavulanate was significantly less (P less than 0.01) at 3 days than at 28 days of age. Values of the major kinetic terms describing the disposition of ticarcillin after i.m. administration to five 3-day-old foals were not significantly different from values of these parameters in the same foals at 28 days of age. After i.m. administration of the drug combination, plasma clavulanate concentrations peaked significantly later (P less than 0.01), and the elimination-rate constant (kd) for clavulanate was significantly less (P less than 0.01), in 3-day-old foals than in 28-day-old foals. The bioavailabilities of ticarcillin and clavulanate after i.m. administration in 3-day-old foals were 100% and 88.3%, respectively, and in 28-day-old foals were 100% and 27.4%, respectively. Mean plasma ticarcillin concentrations exceeded 16 micrograms/ml for a longer period after i.m. administration of the drug combination than after i.v. administration to foals of both age groups. By virtue of the frequency of administration required and the painful response elicited by i.m. injection, it is recommended that when the combination of ticarcillin disodium (50 mg/kg) and clavulanate potassium (1.67 mg/kg) is used in foals to treat infections caused by susceptible organisms (MIC less than or equal to 16 micrograms/ml), it should be administered i.v. four times daily.
在3日龄和28日龄的健康幼驹组中,静脉注射(i.v.)或肌肉注射(i.m.)羧噻吩青霉素二钠(50mg/kg)联合棒酸钾(1.67mg/kg)后,测定了羧噻吩青霉素和棒酸的药代动力学及生物利用度。对5匹幼驹静脉注射该联合制剂后,羧噻吩青霉素和棒酸的处置动力学最好用二室开放模型来描述。与28日龄的幼驹相比,3日龄幼驹中羧噻吩青霉素的平均血浆消除速率常数(β)和清除率(ClB)显著更低(P<0.01),稳态分布容积(Vd(ss))显著更大(P<0.05)。这表明3日龄幼驹的肾排泄机制不成熟,羧噻吩青霉素在其体内分布更广泛。棒酸的平均消除速率常数在3日龄时比28日龄时显著更低(P<0.01)。对5匹3日龄幼驹肌肉注射后,描述羧噻吩青霉素处置的主要动力学参数值与这些幼驹28日龄时的参数值无显著差异。肌肉注射该联合制剂后,3日龄幼驹血浆中棒酸浓度达到峰值的时间显著更晚(P<0.01),棒酸的消除速率常数(kd)显著更低(P<0.01)。3日龄幼驹肌肉注射后羧噻吩青霉素和棒酸的生物利用度分别为100%和88.3%,28日龄幼驹则分别为100%和27.4%。与静脉注射给药的两组幼驹相比,肌肉注射该联合制剂后,幼驹血浆中羧噻吩青霉素浓度超过16μg/ml的持续时间更长。鉴于所需的给药频率以及肌肉注射引起的疼痛反应,建议在幼驹中使用羧噻吩青霉素二钠(50mg/kg)联合棒酸钾(1.67mg/kg)治疗由敏感菌(MIC≤16μg/ml)引起的感染时,应每日静脉注射4次。