Tsuji M, Ishii Y, Ohno A, Miyazaki S, Yamaguchi K
Department of Microbiology, Toho University School of Medicine, Tokyo, Japan.
Antimicrob Agents Chemother. 1998 Jan;42(1):94-9. doi: 10.1128/AAC.42.1.94.
The in vitro and in vivo antibacterial activities of S-4661, a new 1beta-methylcarbapenem, were compared with those of imipenem, meropenem, biapenem, cefpirome, and ceftazidime. The activity of S-4661 against methicillin-susceptible staphylococci and streptococci was comparable to that of imipenem, with an MIC at which 90% of the strains tested were inhibited (MIC90) equal to 0.5 microg/ml or less. S-4661 was highly active against members of the family Enterobacteriaceae, Haemophilus influenzae, and Moraxella catarrhalis, with MIC90s ranging from 0.032 to 0.5 microg/ml. Against imipenem-resistant Pseudomonas aeruginosa, S-4661 was the most active among test agents (MIC90, 8 microg/ml). Furthermore, S-4661 displayed a high degree of activity against many ceftazidime-, ciprofloxacin-, and gentamicin-resistant isolates of P. aeruginosa. The in vivo efficacy of S-4661 against experimentally induced infections in mice caused by gram-positive and gram-negative bacteria, including penicillin-resistant Streptococcus pneumoniae and drug-resistant P. aeruginosa, reflected its potent in vitro activity and high levels in plasma in mice. We conclude that S-4661 is a promising new carbapenem for the treatment of infections caused by gram-positive and -negative bacteria, including penicillin-resistant S. pneumoniae and drug-resistant P. aeruginosa.
将新型1β-甲基碳青霉烯类药物S-4661的体外和体内抗菌活性与亚胺培南、美罗培南、比阿培南、头孢匹罗和头孢他啶进行了比较。S-4661对甲氧西林敏感葡萄球菌和链球菌的活性与亚胺培南相当,90%受试菌株被抑制时的最低抑菌浓度(MIC90)等于或小于0.5微克/毫升。S-4661对肠杆菌科细菌、流感嗜血杆菌和卡他莫拉菌具有高度活性,MIC90范围为0.032至0.5微克/毫升。对于耐亚胺培南的铜绿假单胞菌,S-4661在受试药物中活性最强(MIC90为8微克/毫升)。此外,S-4661对许多耐头孢他啶、环丙沙星和庆大霉素的铜绿假单胞菌分离株也表现出高度活性。S-4661对小鼠实验性诱导感染(由革兰氏阳性和革兰氏阴性细菌引起,包括耐青霉素肺炎链球菌和耐药铜绿假单胞菌)的体内疗效反映了其强大的体外活性以及在小鼠血浆中的高浓度。我们得出结论,S-4661是一种有前景的新型碳青霉烯类药物,可用于治疗由革兰氏阳性和阴性细菌引起的感染,包括耐青霉素肺炎链球菌和耐药铜绿假单胞菌。