山羊静脉给药后阿莫西林/卡维酸联合用药及单独用药的药代动力学

E. Escudero, C.M. Carceles, S. Vicente
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引用次数: 22

摘要

在对10只山羊进行单剂量静脉(i.v)给药后,研究了阿莫西林/克拉维酸组合(25 mg kg - 1)和两种药物单独(阿莫西林20 mg kg - 1)、克拉维酸5 mg kg - 1)的药代动力学行为。目的是确定这些药物联合使用或单独使用时是否存在血浆动力学的差异。采用室间药代动力学和非室间药代动力学方法分析血浆浓度-时间数据。两种药物单独和联合用药的处置曲线最好用双指数方程(双室开放模型)来描述。阿莫西林单用和联用的消除半衰期分别为1.05±0.09 h和1.13±0.19 h,克拉维酸的消除半衰期分别为0.87±0.07 h和0.85±0.09 h。阿莫西林和克拉维酸的表观分布体积在两种治疗中相似。阿莫西林的机体清除率分别为0.12±0.01 l h−1·kg和0.11±0.01 l h−1·kg,克拉维酸的机体清除率分别为0.12±0.02 l h−1·kg和0.12±0.01 l h−1·kg。阿莫西林和克拉维酸的半衰期和体内清除率在单独和联合使用时没有显著差异。结论是,九。阿莫西林和西维酸作为组合产品的管理没有改变任何药物的处置动力学。
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Pharmacokinetics of amoxicillin/ciavulanic acid combination and of both drugs alone after intravenous administration to goats

The pharmacokinetic behaviour of an amoxicillin/clavulanic acid combination(25 mg kg−1), and both drugs alone (amoxicillin 20 mg kg−1), clavulanic acid 5 mg kg−1), was studied after intravenous (i.v.) administration of single doses to 10 goats. The objective was to determine whether there were differences in the plasma kinetics of these drugs when administered in combination or alone. The plasma concentration-time data were analysed by compartmental pharmacokinetics and non-compartmental methods. The disposition curves for both drugs alone and in combination were best described by a biexponential equation (two-compartment open model). The elimination half-lives of amoxicillin were 1.05±0.09 h alone and 1.13±0.19 h in combination, and those of clavulanic acid were 0.87±0.07 h and 0.85±0.09 h, respectively. The apparent volumes of distribution of amoxicillin and clavulanic acid were similar in the two treatments. Body clearances of amoxicillin were 0.12±0.01 l h−1 · kg alone and 0.11±0.01 l h−1 · kg in combination, and of clavulanic acid were 0.12±0.02 l h−1 · kg alone and 0.12±0.01 l h−1 · kg in combination with amoxicillin. The half-lives and body clearances of amoxicillin and clavulanic acid did not differ significantly when administered alone and in combination. It was concluded that the ix. administration of amoxicillin and ciavulanic acid as a combination product did not alter the disposition kinetics of either drug.

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