阿莫西林在实验性肾、肝损伤大鼠体内药代动力学的变化。

Veterinarno-meditsinski nauki Pub Date : 1987-01-01
L Lashev, J Fink-Gremels
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引用次数: 0

摘要

研究了三水合阿莫西林对实验性肾(铬酸钾)和肝(四氯甲烷)损伤的白化大鼠口服阿莫西林的血药浓度和基本药动学参数(kel、Cop、t1 /2、AUC)的影响。结果发现,这些器官的损伤改变了抗生素的吸收、分布和排泄程度。
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[Changes in amoxicillin pharmacokinetics in white rats with experimentally damaged kidneys and liver].

The blood level and the basic pharmacokinetic parameters (kel, Cop, T 1/2, AUC) of amoxicillin trihydrate were studied following its oral application to albino rats with experimentally injured kidneys (potassium chromate) and liver (tetrachloromethane). It was found that the impairment of these organs changed the extent of absorption, distribution, and excretion of the antibiotic.

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