Smith J A, Henry D A
Division of Medical Microbiology, Vancouver General Hospital, British Columbia, Canada.
J Antimicrob Chemother. 1988 Dec;22(6):849-55. doi: 10.1093/jac/22.6.849.
The efficacy of ceftazidime, piperacillin, tobramycin and ticarcillin was tested in vitro against 102 clinical isolates of Pseudomonas aeruginosa. The MIC and MBC of each agent alone were determined. In addition, the rate of killing of 27 isolates by each beta-lactam agent was tested both singly and in combination with tobramycin. The concentrations of beta-lactams and of tobramycin were tailored to each organism; these were double the MBC in the case of the beta-lactams and half the MBC for tobramycin. Although 85.2% of isolates were susceptible to piperacillin and only 58.8% were susceptible to ticarcillin, the MBC90 was higher for piperacillin (greater than 256 mg/l) than ticarcillin (199.7 mg/l). The addition of tobramycin in sublethal concentrations increased the rapidity of killing of bacteria.
对头孢他啶、哌拉西林、妥布霉素和替卡西林的体外抗菌效果进行了测试,受试对象为102株临床分离的铜绿假单胞菌。测定了每种药物单独使用时的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。此外,还测试了27株分离菌对每种β-内酰胺类药物单独使用以及与妥布霉素联合使用时的杀菌速率。β-内酰胺类药物和妥布霉素的浓度根据每种菌株进行调整;β-内酰胺类药物的浓度为MBC的两倍,妥布霉素的浓度为MBC的一半。尽管85.2%的分离菌对哌拉西林敏感,只有58.8%的分离菌对替卡西林敏感,但哌拉西林的MBC90(大于256mg/L)高于替卡西林(199.7mg/L)。添加亚致死浓度的妥布霉素可提高细菌的杀菌速度。