Sakata Y, Boccazzi A, McCracken G H
Antimicrob Agents Chemother. 1983 Feb;23(2):213-7. doi: 10.1128/AAC.23.2.213.
The pharmacokinetics and bacteriological effect of ceftazidime were evaluated in rabbits experimentally infected with Streptococcus pneumoniae, Haemophilus influenzae type b, and Escherichia coli K1. The mean penetration of ceftazidime into cerebrospinal fluid after single-dose or constant-infusion administration ranged from 7.8 to 14.9%. The median cerebrospinal fluid bactericidal titers were 1:64 against S. pneumoniae and H. influenzae and 1:128 against E. coli. The bacterial colony counts in cerebrospinal fluid were reduced by 58% to 100% (-2.3 to -3.9 log10 CFU/ml) in 3 h and by 100% (-3.2 to -5.1 log10 CFU/ml) in 9 h of constant infusion, whereas in untreated infected animals, bacterial counts increased from +1.4 to +2.1 log10 CFU/ml in 9 h. These data on ceftazidime compare favorably with those on penicillin, chloramphenicol, netilmicin, and moxalactam in this experimental meningitis model.
在实验感染肺炎链球菌、b型流感嗜血杆菌和大肠杆菌K1的家兔中评估了头孢他啶的药代动力学和细菌学效应。单剂量或持续输注给药后,头孢他啶进入脑脊液的平均渗透率为7.8%至14.9%。脑脊液杀菌效价中位数对肺炎链球菌和b型流感嗜血杆菌为1:64,对大肠杆菌为1:128。持续输注3小时,脑脊液中的细菌菌落计数减少了58%至100%(-2.3至-3.9 log10 CFU/ml),9小时减少了100%(-3.2至-5.1 log10 CFU/ml),而在未治疗的感染动物中,9小时内细菌计数从+1.4增至+2.1 log10 CFU/ml。在该实验性脑膜炎模型中,头孢他啶的这些数据优于青霉素、氯霉素、奈替米星和莫拉卡坦的数据。