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头孢噻吩在母马体内的药代动力学和生物利用度。

Pharmacokinetics and bioavailability of cephalothin in horse mares.

作者信息

Ruoff W W, Sams R A

出版信息

Am J Vet Res. 1985 Oct;46(10):2085-90.

PMID:4062011
Abstract

The pharmacokinetics and bioavailability of cephalothin given to 6 horse mares at a dosage level of 11 mg/kg of body weight IV or IM were investigated. The disposition of cephalothin given IV was characterized by a rapid disposition phase with a mean half-life of 2.89 minutes and a subsequent slower elimination phase with a mean half-life of only 14.7 minutes. The mean residence time of cephalothin was 10.6 +/- 2.11 minutes. The total plasma clearance of cephalothin averaged 13.6 ml/min/kg and was caused by metabolism and renal elimination. Renal clearance of cephalothin averaged 1.32 ml/min/kg and accounted for elimination of about 10.1% of the administered dose. The volume of distribution at steady state averaged 151 mg/kg. Plasma protein binding of cephalothin at a concentration of 10 micrograms/ml averaged 17.9 +/- 2.5%. Cephalothin was rapidly metabolized to desacetylcephalothin. Maximum plasma desacetylcephalothin concentrations were observed in the blood samples collected 5 minutes after IV doses and averaged 22.9 micrograms/ml. The apparent half-life of desacetylcephalothin in plasma was 41.6 minutes and its renal clearance averaged 4.49 +/- 2.43 ml/min/kg. An average of 33.9% of the dose was recovered in the urine as desacetylcephalothin. The maximum plasma cephalothin concentration after IM administration was 11.3 +/- 3.71 micrograms/ml. The terminal half-life was 47.0 minutes and was longer than the half-life after IV administration. The bioavailability of cephalothin given IM ranged from 38.3% to 93.1% and averaged 65.0 +/- 20.5%.

摘要

研究了以11mg/kg体重的剂量静脉注射(IV)或肌肉注射(IM)头孢噻吩给6匹母马后的药代动力学和生物利用度。静脉注射头孢噻吩的处置特征为快速处置相,平均半衰期为2.89分钟,随后是较慢的消除相,平均半衰期仅为14.7分钟。头孢噻吩的平均驻留时间为10.6±2.11分钟。头孢噻吩的总血浆清除率平均为13.6ml/(min·kg),由代谢和肾脏清除引起。头孢噻吩的肾脏清除率平均为1.32ml/(min·kg),约占给药剂量消除的10.1%。稳态分布容积平均为151mg/kg。头孢噻吩在浓度为10μg/ml时的血浆蛋白结合率平均为17.9±2.5%。头孢噻吩迅速代谢为去乙酰头孢噻吩。静脉注射给药后5分钟采集的血样中观察到最大血浆去乙酰头孢噻吩浓度,平均为22.9μg/ml。去乙酰头孢噻吩在血浆中的表观半衰期为41.6分钟,其肾脏清除率平均为4.49±2.43ml/(min·kg)。平均33.9%的剂量以去乙酰头孢噻吩的形式在尿液中回收。肌肉注射后血浆头孢噻吩的最大浓度为11.3±3.71μg/ml。终末半衰期为47.0分钟,比静脉注射后的半衰期长。肌肉注射头孢噻吩的生物利用度范围为38.3%至93.1%,平均为65.0±20.5%。

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