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阿莫西林和克拉维酸钾复合制剂的药物动力学 被引量:10

Pharmacokinetics of amoxicillin and clavulanic acid co-formulation
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摘要 本文对阿莫西林-克拉维酸钾复合制剂在9名健康成人中进行药物代谢动力学和生物利用度研究。血浆中药物浓度分别用藤黄八叠球菌和克雷伯氏肺炎杆菌为检定菌(用井式琼脂平板法)测定阿莫西林和克拉维田钾。单剂量口服250mg阿莫西林和125mg克拉维酸钾后其阿莫西林的Tmax1.17±0.31hfo0.97±0.33h;Cmax3.5±0.6μg/ml和3.6±0.7μgml;T1/21.1±0.3h和1.15±0.27h。克拉维酸钾为:Tmax1.ll±0.24h和0.89±0.29h;Cmax3.6±1.0μg/ml和4.0±1.44μg/ml;T1/20.78±0.19h和0.8±0.4h。颗粒剂的相对生物利用度阿莫西林为104±20%,克拉维酸钾为108±11%。 moxicillin co-formulation is a new antibacterial agent in which clavulanic acid is a new β-lactamase inhibitor.In this paper ,microbiological assay was described. Amoxicillin was detected by a hole-in-plate with sarciva lutea asthe test organism. Clavulanic acid was determined with klebsiella pneumoniae 41164 as the test organism. The phar-macokinetics of single dose of amoxicillin at 250 mg after orall administration were Tmax 1. 17h and 0. 97h,Cmax3. 5ug/ml and 3. 6ug/ml ,T1/2 1. 10h and 1.15h (tablets and granules) . Pharmacokinetic parameters of clavulanic acid at125mg after orall administration were Tmax 1. 11h and 0. 89h, Cmax 3. 6ug/ml and 4.0ug/ml, T1/20. 78h and 0. 84h(tablets and granules). The relative bioavailability of AMX and CAV granules formulation was 104±20% and 108±11%, respectively.
出处 《中国医院药学杂志》 CAS CSCD 北大核心 1996年第5期197-199,共3页 Chinese Journal of Hospital Pharmacy
关键词 阿莫西林 克拉维酸钾 药物动力学 生物利用度 amoxicillin,clavulanic acid, pharrnacukinetic
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