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头孢曲松的人体药理学(作者译)

[Human pharmacology of ceftriaxone (author's transl)].

作者信息

Le Van Thoi J, Koumare B, Lhoste F, Soussy C J, Duval J

出版信息

Pathol Biol (Paris). 1982 Jun;30(6):345-7.

PMID:6287386
Abstract

The human pharmacology of ceftriaxone was studied in five healthy adult subjects receiving a 500 mg dose intravenously. Evolution of serum levels represents a two compartment open model; the distribution volumes, central and peripheric, were low (about 3 L); the elimination half-life was particularly long : 7.87 hours; the renal and serum clearances and low. These data are probably related to the high affinity of the drug for serum proteins (95 p. cent bound); they suggest once daily parenteral dosing.

摘要

在5名接受500毫克静脉注射剂量的健康成年受试者中研究了头孢曲松的人体药理学。血清水平的变化呈现二室开放模型;中央室和外周室的分布容积较低(约3升);消除半衰期特别长:7.87小时;肾清除率和血清清除率较低。这些数据可能与该药物对血清蛋白的高亲和力(95%结合)有关;它们提示每日一次肠胃外给药。

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