Dubb J, Actor P, Pitkin D, Alexander F, Familiar R, Ehrlich S, Stote R
Clin Pharmacol Ther. 1982 Apr;31(4):516-21. doi: 10.1038/clpt.1982.69.
The kinetics and renal handling of ceftizoxime were examined after intravenous and intramuscular injection and the effect of probenecid on its excretion was investigated. Peak serum level after 1000 mg IV was 60.5 microgram/ml and half-life (t 1/2) was 1.4 hr. Peak serum level (40.9 microgram/ml) was reached 1 hr after 1000 mg IM. When probenecid was added to the 1000-mg IM dose the peak level was 44.3 microgram/ml at 1 hr and serum levels at 2, 4, 6, and 8 hr were all higher than after ceftizoxime alone (P less than 0.01). The 1.85-hr t 1/2 of ceftizoxime alone was extended to 2.29 hr when probenecid was added. Ceftizoxime was shown to be actively secreted by the renal tubule; this secretion was decreased by probenecid.
静脉注射和肌肉注射后,对头孢唑肟的动力学和肾脏处理情况进行了研究,并考察了丙磺舒对其排泄的影响。静脉注射1000毫克后血清峰值水平为60.5微克/毫升,半衰期(t1/2)为1.4小时。肌肉注射1000毫克后1小时达到血清峰值水平(40.9微克/毫升)。当丙磺舒加入到1000毫克肌肉注射剂量中时,1小时时的峰值水平为44.3微克/毫升,并且在2、4、6和8小时时的血清水平均高于单独使用头孢唑肟后的水平(P<0.01)。单独使用头孢唑肟时1.85小时的t1/2在加入丙磺舒后延长至2.29小时。头孢唑肟显示可被肾小管主动分泌;丙磺舒可减少这种分泌。