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肌肉注射后氯霉素在奶牛体内的药代动力学。

Pharmacokinetics of chloramphenicol in cows after intramuscular application.

作者信息

Tanner U, Wuethrich A

出版信息

Vet Res Commun. 1985 Feb;9(1):25-34. doi: 10.1007/BF02215125.

Abstract

The concentrations of chloramphenicol and its water-soluble metabolites in the plasma of six clinically healthy heifers were measured at intervals during five days after intramuscular administration of free chloramphenicol (20 mg/kg) in a vehicle containing 40% of an organic solvent. Estimations were carried out by a colorimetric method and by high pressure liquid chromatography (for the very low values beyond the second day). For free chloramphenicol a peak concentration of 1.7 micrograms/ml at 7.3 h after injection was found (MIC: 5 micrograms/ml). Bioavailability was calculated to be 63%. It is shown that absorption was apparently not a uniform process but occurred rather slowly (t 1/2 (ab) = 10.2 h) for the main part of the available dose, whereas one sixth was quickly absorbed (t'1/2 (ab) = 0.7 h). The apparent half-time of elimination was 10.2 h for the unchanged drug. At the fifth day after administration the plasma concentration was below the limit of detectability (10 ng/ml) in all animals.

摘要

在六头临床健康的小母牛肌肉注射含40%有机溶剂载体的游离氯霉素(20毫克/千克)后的五天内,定期测定其血浆中氯霉素及其水溶性代谢物的浓度。采用比色法和高压液相色谱法(用于第二天之后的极低值)进行测定。对于游离氯霉素,注射后7.3小时的峰值浓度为1.7微克/毫升(最低抑菌浓度:5微克/毫升)。计算得出生物利用度为63%。结果表明,吸收显然不是一个均匀的过程,可用剂量的主要部分吸收相当缓慢(吸收半衰期t 1/2(ab)=10.2小时),而六分之一迅速吸收(吸收半衰期t'1/2(ab)=0.7小时)。未变化药物的表观消除半衰期为10.2小时。给药后第五天,所有动物的血浆浓度均低于可检测限(10纳克/毫升)。

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