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药代动力学:喹诺酮类药物在人体内的代谢及经肾排泄情况

Pharmacokinetics: metabolism and renal excretion of quinolones in man.

作者信息

Vree T B, Wijnands W J, Guelen P J, Baars A M, Hekster Y A

出版信息

Pharm Weekbl Sci. 1986 Feb 21;8(1):29-34. doi: 10.1007/BF01975476.

Abstract

The quinolones are relatively poorly absorbed from the gastrointestinal tract. The elimination proceeds mainly by renal excretion. The half-life of elimination depends on the molecular structure and varies between 2 and 10 h. Impaired kidney function is expected to increase the half-life of elimination, though this effect is not always observed. Since the 4-oxo-metabolites show a higher renal clearance than the parent drug, renal impairment will result in a cumulation of the metabolites in the body.

摘要

喹诺酮类药物从胃肠道的吸收相对较差。消除主要通过肾脏排泄进行。消除半衰期取决于分子结构,在2至10小时之间变化。肾功能受损预计会增加消除半衰期,尽管并非总是观察到这种效应。由于4-氧代代谢物的肾脏清除率高于母体药物,肾功能损害将导致代谢物在体内蓄积。

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