Chan M K, Chau P Y, Chan W W
Department of Medicine, University of Hong Kong, Queen Mary Hospital.
Clin Nephrol. 1987 Dec;28(6):277-80.
Pharmacokinetics of ofloxacin (OFX) was studied in patients on continuous ambulatory peritoneal dialysis (CAPD) carrying out three exchanges per day. In 11 patients given 300 mg of OFX orally, serum OFX concentration peaked at 2.44 mg/l 3.7 hours after administration and the mean elimination half-life of OFX was 25 hours. OFX concentrations in peritoneal fluid underwent cyclical changes with each change of solutions, reaching beyond 0.5 mg/l after 2 hours of equilibration. There was a highly significant correlation between corresponding serum and peritoneal fluid concentrations of OFX after an 8 h equilibration (r = 0.85, p less than 0.001). In 5 patients given a 400 mg loading dose followed by 200 mg of OFX per day for 7 days, trough serum OFX concentrations ranged from 1.35 to 7.00 mg/l and no adverse effects were noticed. CAPD per exchange removed less than 2% of the total dose of OFX given.
在每天进行三次交换的持续性非卧床腹膜透析(CAPD)患者中研究了氧氟沙星(OFX)的药代动力学。11名口服300mg OFX的患者,给药后3.7小时血清OFX浓度达到峰值2.44mg/L,OFX的平均消除半衰期为25小时。随着每次溶液更换,腹膜液中OFX浓度呈周期性变化,平衡2小时后超过0.5mg/L。8小时平衡后,OFX相应的血清和腹膜液浓度之间存在高度显著相关性(r = 0.85,p小于0.001)。5名患者给予400mg负荷剂量,随后每天给予200mg OFX,共7天,血清OFX谷浓度范围为1.35至7.00mg/L,未观察到不良反应。每次CAPD交换清除的OFX总量不到给药总量的2%。