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头孢乙腈——药代动力学数据在剂量确定中的应用。

Cephacetrile--application of pharmacokinetic data to dosage determination.

作者信息

Brogard J M, Dorner M, Brandt C, Lavillaureix J

出版信息

Int J Clin Pharmacol Biopharm. 1976 Apr;13(3):168-76.

PMID:950258
Abstract

This pharmacokinetic investigation was based on the determination of serum and urinary levles of cephacetrile in 50 subjects given single intramuscular or intravenous doses of 0.5 or 1 gm of the antibiotic; 30 normal subjects, 10 patients with renal insufficiency, and 10 patients with chronic nephritis undergoing maintenance haemodialysis were included in this study. In normal subjects, mean serum half-life was 1.09 hours (Ke = 0.6337) after intramuscular injection of 0.5 gm cephacetrile, 1.31 hours (Ke = 0.5276) after intramuscular injection of 1 gm, and 0.89 hours (Ke = 0.7806) after intravenous injection of 1 gm. Absorption half-life was 0.45 hours after intramuscular injection of 1 gm cephacetrile. The urinary elimination of cephacetrile over the first 6 hours after injection was on the average 72.7% of the administered dose. After intravenous injection of 1 gm of the antibiotic, the plasma clearance of cephacetrile was 407 ml/min., and its renal clearance 313 ml/min. A linear correlation was found between the values of overall elimination rate constant (Ke) and creatinine clearance in the subjects under investigation (Ke = 0.0080 + 0.0061 ClCr). The established pharmacokinetic characteristics were used to calculate the maintenance and loading doses as well as the intervals between injections adjusted to creatinine clearance. These data constitute true dosage schemes adapted to the particular case of each patient according to his kidney function.

摘要

这项药代动力学研究基于对50名单次肌内或静脉注射0.5克或1克该抗生素的受试者血清和尿液中头孢乙腈水平的测定;该研究纳入了30名正常受试者、10名肾功能不全患者和10名接受维持性血液透析的慢性肾炎患者。在正常受试者中,肌内注射0.5克头孢乙腈后,平均血清半衰期为1.09小时(Ke = 0.6337),肌内注射1克后为1.31小时(Ke = 0.5276),静脉注射1克后为0.89小时(Ke = 0.7806)。肌内注射1克头孢乙腈后的吸收半衰期为0.45小时。注射后前6小时内头孢乙腈的尿排泄量平均为给药剂量的72.7%。静脉注射1克该抗生素后,头孢乙腈的血浆清除率为407毫升/分钟,肾清除率为313毫升/分钟。在所研究的受试者中,总消除速率常数(Ke)值与肌酐清除率之间发现存在线性相关性(Ke = 0.0080 + 0.0061 ClCr)。利用已确定的药代动力学特征来计算维持剂量、负荷剂量以及根据肌酐清除率调整的注射间隔。这些数据构成了根据每位患者的肾功能情况适用于其具体病例的真实给药方案。

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