Intorre L, Mengozzi G, Maccheroni M, Bertini S, Soldani G
Laboratory of Veterinary Pharmacology and Toxicology, University of Pisa, Italy.
J Vet Pharmacol Ther. 1995 Oct;18(5):352-6. doi: 10.1111/j.1365-2885.1995.tb00603.x.
Enrofloxacin, a quinolone antibiotic developed exclusively for use in animals, was investigated for its effects on the steady-state pharmacokinetics of theophylline in six healthy Beagle dogs. A sustained-release theophylline formulation was given alone (20 mg/kg per os twice daily at 12 h intervals) for 9 days and then co-administered with enrofloxacin (5 mg/kg i.v. once a day) for 5 days. Mean trough theophylline concentrations progressively and significantly increased during the five days of enrofloxacin co-administration. Theophylline clearance and concentration-time profile were significantly changed by enrofloxacin co-administration. No significant change was observed in enrofloxacin pharmacokinetics. The kinetic interaction between theophylline and enrofloxacin could be of clinical significance and may require plasma drug concentration monitoring and adjustment of theophylline dosage.
恩诺沙星是一种专门开发用于动物的喹诺酮类抗生素,研究了其对6只健康比格犬体内茶碱稳态药代动力学的影响。一种缓释茶碱制剂单独给药(每12小时口服20mg/kg,每日两次),持续9天,然后与恩诺沙星联合给药(静脉注射5mg/kg,每日一次),持续5天。在恩诺沙星联合给药的5天内,茶碱的平均谷浓度逐渐显著升高。恩诺沙星联合给药显著改变了茶碱的清除率和浓度-时间曲线。恩诺沙星的药代动力学未观察到显著变化。茶碱与恩诺沙星之间的动力学相互作用可能具有临床意义,可能需要进行血浆药物浓度监测并调整茶碱剂量。