Monif G R, Clark P R, Shuster J J, Baer H
Antimicrob Agents Chemother. 1978 Nov;14(5):643-9. doi: 10.1128/AAC.14.5.643.
Sodium piperacillin T-1220, a new semisynthetic penicillin, was tested in vitro against 297 clinical isolates of anaerobic bacteria and 669 aerobic bacteria by the conventional agar dilution method and compared with carbenicillin and ticarcillin. At a 100-mug/ml concentration the three drugs showed comparable effectiveness against the anaerobes tested. However, at 20 mug/ml, piperacillin was the most effective drug against Bacteroides fragilis, peptostreptococci, and group D streptococci. At this drug concentration only 48% of the B. fragilis strains exhibited susceptibility to carbenicillin only, 64% exhibited susceptibility to ticarcillin but 90% exhibited susceptibility to piperacillin. Similar findings were observed with peptostreptococci and group D streptococci. On a weight basis piperacillin was statistically shown to be the most effective antibiotic of the three tested against these anaerobes. At 20 mug/ml, piperacillin exhibited a statistically significant difference (P < 0.01) over carbenicillin and ticarcillin for Serratia marcescens, Escherichia coli, Klebsiella species, Klebsiella pneumoniae, Pseudomonas isolates, and Citrobacter diversus. At both 20- and 100-mug/ml concentrations, piperacillin appeared to be the most effective (calculated P < 0.01) upon Klebsiella species, K. pneumoniae, S. marcescens, and C. freundii in activity over ticarcillin and carbenicillin.
哌拉西林T - 1220钠是一种新型半合成青霉素,采用常规琼脂稀释法对297株厌氧菌临床分离株和669株需氧菌进行了体外测试,并与羧苄西林和替卡西林进行了比较。在100μg/ml浓度下,这三种药物对所测试的厌氧菌显示出相当的有效性。然而,在20μg/ml时,哌拉西林是对脆弱拟杆菌、消化链球菌和D组链球菌最有效的药物。在此药物浓度下,仅48%的脆弱拟杆菌菌株仅对羧苄西林敏感,64%对替卡西林敏感,但90%对哌拉西林敏感。消化链球菌和D组链球菌也有类似的发现。从重量基础来看,统计学表明哌拉西林是所测试的三种药物中对这些厌氧菌最有效的抗生素。在20μg/ml时,对于粘质沙雷氏菌、大肠埃希菌、克雷伯菌属、肺炎克雷伯菌、假单胞菌分离株和奇异柠檬酸杆菌,哌拉西林与羧苄西林和替卡西林相比有统计学显著差异(P < 0.01)。在20μg/ml和100μg/ml浓度下,对于克雷伯菌属、肺炎克雷伯菌、粘质沙雷氏菌和弗氏柠檬酸杆菌,哌拉西林在活性上似乎是最有效的(计算得出P < 0.01),优于替卡西林和羧苄西林。