Montesissa C, Villa R, Sonzogni O, Belloli C, Carli S
Institute of Pharmacology, Pharmacokinetics and Toxicology, Bologna, Italy.
J Vet Pharmacol Ther. 1994 Oct;17(5):359-64. doi: 10.1111/j.1365-2885.1994.tb00259.x.
The pharmacokinetics of ampicillin and sulbactam administered in combination were studied in calves and sheep. The animals were administered an aqueous solution of ampicillin/sulbactam (2:1, w/w) intravenously and intramuscularly at doses of 13.2 and 6.6 mg.kg-1, respectively. A microbiological method was used to detect ampicillin, and HPLC was used to detect sulbactam in serum. Following intravenous (i.v.) administration, the distribution phases were rapid and similar (about 15 min) for both drugs in both species, whereas sulbactam in calves and ampicillin in sheep showed a faster elimination rate. After intramuscular (i.m.) administration both drugs showed peak concentrations higher in calves than in sheep; the peak time of sulbactam was shorter in calves than in sheep. No other significant differences in the pharmacokinetics of the combination were observed between the species after i.m. injection. The mean residence and absorption times, calculated by non-compartmental analysis, for both calves and sheep suggested that the differences in ampicillin and sulbactam pharmacokinetics could be attributable to the different molecular structures.
在犊牛和绵羊中研究了联合使用氨苄西林和舒巴坦的药代动力学。分别以13.2和6.6mg.kg-1的剂量对动物静脉内和肌内注射氨苄西林/舒巴坦(2:1,w/w)水溶液。采用微生物学方法检测血清中的氨苄西林,采用高效液相色谱法检测血清中的舒巴坦。静脉注射后,两种药物在两个物种中的分布阶段都很快且相似(约15分钟),而犊牛中的舒巴坦和绵羊中的氨苄西林显示出更快的消除率。肌内注射后,两种药物在犊牛中的峰值浓度均高于绵羊;舒巴坦在犊牛中的达峰时间比在绵羊中短。肌内注射后,两个物种之间联合用药的药代动力学未观察到其他显著差异。通过非房室分析计算的犊牛和绵羊的平均驻留时间和吸收时间表明,氨苄西林和舒巴坦药代动力学的差异可能归因于不同的分子结构。