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单剂量三水合阿莫西林肌肉注射在短尾矮袋鼠(Macropus eugenii)体内的药代动力学。

The pharmacokinetics of single dose intramuscular amoxicillin trihydrate in tammar wallabies (Macropus eugenii).

作者信息

McLelland David J, Rich Brian G, Holz Peter H

机构信息

University of Guelph, Guelph, Ontario N1G 2W1, Canada.

出版信息

J Zoo Wildl Med. 2009 Mar;40(1):113-6. doi: 10.1638/2008-0104.1.

Abstract

Five tammar wallabies (Macropus eugenii) were injected intramuscularly with 10 mg/kg amoxicillin trihydrate. Serial blood samples were collected through to 26 hr postinjection. Plasma amoxicillin concentrations were measured using high-performance liquid chromatography. Pharmacokinetic parameters were estimated using noncompartmental analysis. The terminal half-life (1.77 +/- 0.40 hr) was comparable to that previously reported in domestic small ruminants. Without intravenous kinetic data, it is unclear whether the terminal phase is elimination- or absorption-dependent; both scenarios have been reported in domestic species. Plasma concentrations of amoxicillin remained above a reported minimum inhibitory concentration (MIC) breakpoint for staphylococci and streptococci for at least 8 hr; the MIC breakpoint for enterobacteria and enterococci was never attained.

摘要

给五只帚尾岩袋鼠(短尾矮袋鼠)肌肉注射10毫克/千克三水合阿莫西林。在注射后持续采集血样直至26小时。使用高效液相色谱法测量血浆阿莫西林浓度。采用非房室分析估算药代动力学参数。终末半衰期(1.77±0.40小时)与先前报道的家养小型反刍动物的半衰期相当。由于没有静脉动力学数据,尚不清楚终末相是消除依赖性还是吸收依赖性;在家养物种中这两种情况均有报道。阿莫西林的血浆浓度至少8小时保持在报道的葡萄球菌和链球菌最低抑菌浓度(MIC)断点以上;肠杆菌和肠球菌的MIC断点从未达到。

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