微生物学
氨苄西林
奇异变形杆菌
产气肠杆菌
粪肠球菌
生物
最小抑制浓度
铜绿假单胞菌
肠杆菌
阿莫西林
大肠杆菌
抗生素
细菌
生物化学
遗传学
基因
作者
MICHAEL J. BASKER,M.N. Gwynn,Anthony R. White
出处
期刊:Chemotherapy
[Karger Publishers]
日期:1979-01-01
卷期号:25 (3): 170-180
被引量:13
摘要
The antibacterial activities of three aminopenicillins ampicillin, epicillin and amoxycillin were compared in vitro and in vivo. The minimum inhibitory concentrations (MIC) of the three penicillins were very similar and the compounds were active against non-β-lactamase-producing strains of Escherichia coli, Salmonella and Shigella species, Proteus mirabilis, Haemophilus influenzae and Neissería gonorrhoeae. Streptococci including Streptococcus faecalis, and non-β-lactamase-producing staphylococci were also sensitive to the compounds but Pseudomonas aeruginosa, Klebsiella aerogenes, Enterobacter and indole-positive Proteus species were resistant. At concentrations close to MIC value epicillin and ampicillin showed similar bactericidal activity against E. coli and against S. typhi and both compounds caused a slower rate of kill than was seen with amoxycillin. Microscopical observation of the cells exposed to ampicillin and epicillin for 1 h showed the presence of filamentous forms which lysed slowly, whereas cells exposed to amoxycillin for the same period lysed rapidly. Epicillin was similar to or slightly less active than ampicillin against experimental mouse infections, and against the majority of infections both compounds were significantly less effective than amoxycillin by the oral and subcutaneous routes of administration.
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