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头孢噻肟在绵羊体内的药代动力学

Pharmacokinetics of cefotaxime in sheep.

作者信息

Guerrini V H, Filippich L, English P B, Bourne D W

出版信息

Am J Vet Res. 1983 Aug;44(8):1488-91.

PMID:6312852
Abstract

Five healthy adult Merino ewes were each given 2 g of cefotaxime by the IV, IM, and subcutaneous (SC) routes. The serial plasma samples collected after each treatment were analyzed for cefotaxime by a new high-pressure liquid chromatographic method. Plasma concentration time profiles were characterized by a linear 2-compartment model after IV administration and the following mean values (+/- SD) were found: biological half-life, 23 +/- 8 minutes; apparent volume of distribution, 5.5 +/- 1.3 L; plasma clearance, 0.37 +/- 0.09 L/min; elimination rate constant, 0.066 +/- 0.014 minute-1; rate of diffusion into tissue, 0.013 +/- 0.013 minute-1; and out of tissue, 0.035 +/- 0.017 minute-1. Plasma cefotaxime concentrations in the ewes given the drug by the IV, IM, and SC routes were 113 +/- 32, 71 +/- 20, and 38 +/- 11 micrograms/ml, respectively, at 15 minutes; 2.31 +/- 0.82, 11.3 +/- 6.6, and 16.4 +/- 3.7 micrograms/ml at 120 minutes; and 1.05 +/- 1.22, 9.3 +/- 5.2, and 14.9 +/- 1.27 micrograms/ml at 150 minutes. After cefotaxime was given SC and IM, plasma values were higher for a longer time than they were after the drug was given IV, probably due to a slower release of drug from the former injection sites.

摘要

五只健康成年美利奴母羊分别通过静脉注射(IV)、肌肉注射(IM)和皮下注射(SC)途径给予2克头孢噻肟。每次给药后采集的系列血浆样本采用一种新的高压液相色谱法分析头孢噻肟。静脉注射后,血浆浓度-时间曲线以线性二室模型表征,得到以下平均值(±标准差):生物半衰期为23±8分钟;表观分布容积为5.5±1.3升;血浆清除率为0.37±0.09升/分钟;消除速率常数为0.066±0.014分钟⁻¹;药物向组织内的扩散速率为0.013±0.013分钟⁻¹;药物从组织内的扩散速率为0.035±0.017分钟⁻¹。通过静脉注射、肌肉注射和皮下注射途径给药的母羊,在15分钟时血浆头孢噻肟浓度分别为113±32、71±20和38±11微克/毫升;在120分钟时分别为2.31±0.82、11.3±6.6和16.4±3.7微克/毫升;在150分钟时分别为1.05±1.22、9.3±5.2和14.9±1.27微克/毫升。头孢噻肟经皮下注射和肌肉注射后,血浆值高于静脉注射给药后的血浆值,且维持时间更长,这可能是由于药物从前述注射部位释放较慢所致。

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