Gootz T D, Sanders C C, Sanders W E
Antimicrob Agents Chemother. 1979 Jun;15(6):783-91. doi: 10.1128/AAC.15.6.783.
The activity of furazlocillin (Bay k 4999) was compared with those of mezlocillin, piperacillin, and standard beta-lactam antibiotics against a number of gram-positive and gram-negative organisms. These new expanded-spectrum penicillins were less active than penicillin G against most gram-positive organisms. Furazlocillin, mezlocillin, and piperacillin showed activity comparable to ampicillin and penicillin G against Haemophilus influenzae and penicillin-susceptible neisseriae, respectively. None of the drugs tested was effective against penicillin-resistant gonococci. The activity of furazlocillin was greater than that of mezlocillin, piperacillin, ampicillin, or carbenicillin against many Enterobacteriaceae. However, certain beta-lactam-resistant strains among these organisms were not highly susceptible to any of the three new penicillins. Furazlocillin was less active than piperacillin against Pseudomonas aeruginosa but was more active than carbenicillin or mezlocillin. Inoculum effects and discrepancies between minimal inhibitory concentrations and minimal bactericidal concentrations were observed with furazlocillin, mezlocillin, and piperacillin against several genera. The kinetics of bacterial killing by the new penicillins were often slow and incomplete over 24 h, especially in tests with Enterobacter and P. aeruginosa. Synergy was demonstrated between furazlocillin and aminoglycosides against a variety of gram-negative bacilli and Streptococcus faecalis.
将呋苄西林(Bay k 4999)与美洛西林、哌拉西林及标准β-内酰胺类抗生素对多种革兰氏阳性菌和革兰氏阴性菌的活性进行了比较。这些新型广谱青霉素对大多数革兰氏阳性菌的活性低于青霉素G。呋苄西林、美洛西林和哌拉西林分别对流感嗜血杆菌和对青霉素敏感的奈瑟菌显示出与氨苄西林和青霉素G相当的活性。所测试的药物均对耐青霉素淋病奈瑟菌无效。呋苄西林对许多肠杆菌科细菌的活性大于美洛西林、哌拉西林、氨苄西林或羧苄西林。然而,这些细菌中的某些β-内酰胺耐药菌株对这三种新型青霉素中的任何一种都不高度敏感。呋苄西林对铜绿假单胞菌的活性低于哌拉西林,但高于羧苄西林或美洛西林。观察到呋苄西林、美洛西林和哌拉西林对几个菌属存在接种物效应以及最小抑菌浓度和最小杀菌浓度之间的差异。新型青霉素的细菌杀灭动力学在24小时内通常缓慢且不完全,尤其是在对肠杆菌和铜绿假单胞菌的测试中。呋苄西林与氨基糖苷类药物对多种革兰氏阴性杆菌和粪肠球菌表现出协同作用。