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首页> 外文期刊>Journal of Veterinary Pharmacology and Therapeutics >Bioavailability and pharmacokinetics of a novel cephalexin oral paste formulation in fed and fasted dogs
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Bioavailability and pharmacokinetics of a novel cephalexin oral paste formulation in fed and fasted dogs

机译:新型头孢氨苄口服糊剂制剂在喂食和禁食狗中的生物利用度和药代动力学

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摘要

Cephalexin is a Group 2 (first generation) cephalosporin with excellent activity against many Gram-positive bacteria including beta-lactamase-producing Staphylococcus spp. It appears rapidly absorbed after oral administration in dogs and excreted unchanged in the urine by glomerular filtration and tubular secretion (Prescott, 2006). No veterinary formulation of cephalexin is available in North America, but numerous human oral formulations are used for skin infections in small animal practice. Human parenteral formulations are also available in other markets (Rebuelto et al., 2005), though none is currently available in North America.
机译:头孢氨苄是第2组(第一代)头孢菌素,对许多革兰氏阳性细菌(包括产生β-内酰胺酶的葡萄球菌属)具有出色的活性。它在狗口服后似乎迅速吸收,并通过肾小球滤过和肾小管分泌物在尿液中不变地排泄(Prescott,2006)。在北美,没有头孢氨苄的兽用制剂,但是在小动物实践中,许多人类口服制剂被用于皮肤感染。人肠胃外制剂也可在其他市场上获得(Rebuelto等,2005),尽管北美目前没有。

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