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同时静脉输注后头孢唑林和拉氧头孢的药代动力学

Cefazolin and moxalactam pharmacokinetics after simultaneous intravenous infusion.

作者信息

Polk R E, Kline B J, Markowitz S M

出版信息

Antimicrob Agents Chemother. 1981 Nov;20(5):576-9. doi: 10.1128/AAC.20.5.576.

Abstract

A high-performance liquid chromatographic method for the measurement of moxalactam concentrations in serum was modified to permit the simultaneous measurement of both moxalactam and cefazolin. We then studied whether the simultaneous administration of both moxalactam and cefazolin to normal subjects would produce profiles of serum concentration versus time which were the same as those obtained after the administration of each drug individually. Six healthy adults received a 30-min infusion of cefazolin (10 mg/kg), followed in 2 days by the same dose of moxalactam. After 2 days, both antibiotics were administered together. A two-compartment model was found to adequately characterize the data, and the serum concentration curve for each drug when given alone was statistically identical to that obtained after simultaneous administration. Cefazolin was found to produce a significantly greater peak serum concentration (105 +/- 14 versus 81 +/- 21 microgram/ml) and a significantly greater area under the curve (218 +/- 42 versus 157 +/- 19 . microgram h/ml). The terminal half-life of moxalactam was not significantly longer than for cefazolin (2.2 +/- 0.6 versus 2.0 +/- 0.6 h, respectively). The method of simultaneous administration may have distinct advantages over conventional methods for studies of comparative tissue penetration.

摘要

一种用于测定血清中莫西沙星浓度的高效液相色谱法被改进,以允许同时测定莫西沙星和头孢唑林。然后,我们研究了对正常受试者同时给予莫西沙星和头孢唑林是否会产生与单独给予每种药物后获得的血清浓度-时间曲线相同的曲线。六名健康成年人接受了30分钟的头孢唑林输注(10mg/kg),两天后给予相同剂量的莫西沙星。两天后,两种抗生素一起给药。发现二室模型足以表征数据,每种药物单独给药时的血清浓度曲线与同时给药后获得的曲线在统计学上相同。发现头孢唑林产生的血清峰值浓度显著更高(105±14对81±21μg/ml),曲线下面积显著更大(218±42对157±19.μg·h/ml)。莫西沙星的终末半衰期并不比头孢唑林显著更长(分别为2.2±0.6对2.0±0.6小时)。对于比较组织渗透的研究,同时给药的方法可能比传统方法具有明显优势。

相似文献

5
Moxalactam--absorption, excretion, distribution, and metabolism.
Rev Infect Dis. 1982 Nov-Dec;4 Suppl:S569-80. doi: 10.1093/clinids/4.supplement_3.s569.

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