Fernandez Lastra C, Mariño E L, Dominguez-Gil A
Department of Pharmacy, School of Pharmacy, University of Salamanca, Spain.
Arzneimittelforschung. 1987 Aug;37(8):927-9.
The evolution of phosphomycin (Fosfocina), levels in serum and experimentally induced interstitial tissue fluid and the access of the drug to different organs were studied in rabbits after the administration of a single dose of 60 mg/kg and during a multiple dosage regimen of 60 mg/kg/6 h over three days. Following the administration of a single dose a Cmax value of phosphomycin in interstitial tissue fluid of 80.4 micrograms/ml was reached at 1.2 h. The elimination half-life of the drug from the systemic circulation after a single dose had a value of 1.6 h, and was not significantly different from the value found for the same parameter in the multiple dosage regimen. The disappearance half-life of phosphomycin from interstitial tissue fluid, with a value of 1.9 h for the single dose schedule, was not significantly different from the value of the disappearance half-life of the drug from interstitial tissue fluid in the multiple dosage regimen. Finally, the results of the present study confirm the linearity of phosphomycin kinetics, at least in the conditions studied, and show that the drug is not accumulated in the organs considered.
在给予家兔单次剂量60mg/kg以及连续三天每天按60mg/kg、每6小时给药一次的多剂量方案给药后,研究了磷霉素(Fosfocina)的演变、血清及实验诱导的间质组织液中的水平以及药物在不同器官中的分布情况。单次给药后,在1.2小时时间质组织液中磷霉素的Cmax值达到80.4微克/毫升。单次给药后药物从体循环中的消除半衰期为1.6小时,与多剂量方案中相同参数的值无显著差异。单次给药方案中间质组织液中磷霉素的消除半衰期为1.9小时,与多剂量方案中间质组织液中药物消除半衰期的值无显著差异。最后,本研究结果证实了磷霉素动力学的线性,至少在所研究的条件下是如此,并且表明该药物在所考虑的器官中不会蓄积。