Arvidsson A, Alván G, Tranaeus A, Malmborg A S
Eur J Clin Pharmacol. 1985;28(3):333-7. doi: 10.1007/BF00543333.
The pharmacokinetics of cefoxitin was examined in 9 patients undergoing peritoneal dialysis for chronic renal failure. Cefoxitin was administered intraperitoneally in the dialysate fluid every 6 h for 24 h, in two different concentrations, 50 micrograms/ml and 100 micrograms/ml. The plasma half-life of cefoxitin was 20.2 h. The major route of elimination was non-renal, with a clearance of 8.0 ml/min. Peritoneal clearance was 4.1 ml/min. As expected, renal clearance was negligible. The peak plasma concentrations of cefoxitin at the two dose levels used were 7 micrograms/ml and 15 micrograms/ml, respectively, when assayed by HPLC, and 12 micrograms/ml and 24 micrograms/ml when determined by a microbiological assay. The cefoxitin concentration in the dialysate decreased from 50 micrograms/ml to 14 micrograms/ml and from 100 micrograms/ml to 37 micrograms/ml during the 6 h of its retention in the peritoneal cavity.
对9例慢性肾衰竭接受腹膜透析的患者进行了头孢西丁的药代动力学研究。将头孢西丁以两种不同浓度(50微克/毫升和100微克/毫升)加入透析液中,每6小时经腹腔给药一次,共给药24小时。头孢西丁的血浆半衰期为20.2小时。主要消除途径为非肾途径,清除率为8.0毫升/分钟。腹膜清除率为4.1毫升/分钟。正如预期的那样,肾清除率可忽略不计。采用高效液相色谱法测定时,所用两个剂量水平的头孢西丁血浆峰浓度分别为7微克/毫升和15微克/毫升,采用微生物测定法测定时分别为12微克/毫升和24微克/毫升。在头孢西丁于腹腔内保留的6小时内,透析液中头孢西丁浓度从50微克/毫升降至14微克/毫升,从100微克/毫升降至37微克/毫升。