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新型广谱肠外碳青霉烯类药物SM-216601的体外和体内抗菌活性

In vitro and in vivo antibacterial activities of SM-216601, a new broad-spectrum parenteral carbapenem.

作者信息

Ueda Yutaka, Kanazawa Katsunori, Eguchi Ken, Takemoto Koji, Eriguchi Yoshiro, Sunagawa Makoto

机构信息

Sumitomo Pharmaceuticals Research Division, Konohana, Osaka, Japan.

出版信息

Antimicrob Agents Chemother. 2005 Oct;49(10):4185-96. doi: 10.1128/AAC.49.10.4185-4196.2005.

Abstract

SM-216601 is a novel parenteral 1beta-methylcarbapenem. In agar dilution susceptibility testing, the MIC of SM-216601 for 90% of the methicillin-resistant Staphylococcus aureus (MRSA) strains tested (MIC(90)) was 2 microg/ml, which was comparable to those of vancomycin and linezolid. SM-216601 was also very potent against Enterococcus faecium, including vancomycin-resistant strains (MIC(90) = 8 microg/ml). SM-216601 exhibited potent activity against penicillin-resistant Streptococcus pneumoniae, ampicillin-resistant Haemophilus influenzae, Moraxella catarrhalis, Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis, with MIC(90)s of less than 0.5 microg/ml, and intermediate activity against Citrobacter freundii, Enterobacter cloacae, Serratia marcescens, and Pseudomonas aeruginosa. The therapeutic efficacy of SM-216601 against experimentally induced infections in mice caused by S. aureus, E. faecium, E. coli, and P. aeruginosa reflected its in vitro activity and plasma level. Thus, SM-216601 is a promising candidate for nosocomial bacterial infections caused by a wide range of gram-positive and gram-negative bacteria, including multiresistant pathogens.

摘要

SM - 216601是一种新型的肠胃外注射用1β - 甲基碳青霉烯类药物。在琼脂稀释药敏试验中,SM - 216601对90%的受试耐甲氧西林金黄色葡萄球菌(MRSA)菌株的最低抑菌浓度(MIC90)为2微克/毫升,这与万古霉素和利奈唑胺相当。SM - 216601对粪肠球菌也非常有效,包括耐万古霉素菌株(MIC90 = 8微克/毫升)。SM - 216601对耐青霉素肺炎链球菌、耐氨苄西林流感嗜血杆菌、卡他莫拉菌、大肠杆菌、肺炎克雷伯菌和奇异变形杆菌表现出强效活性,MIC90小于0.5微克/毫升,对弗氏柠檬酸杆菌、阴沟肠杆菌、黏质沙雷菌和铜绿假单胞菌具有中等活性。SM - 216601对小鼠由金黄色葡萄球菌、粪肠球菌、大肠杆菌和铜绿假单胞菌引起的实验性感染的治疗效果反映了其体外活性和血浆水平。因此,SM - 216601是治疗由多种革兰氏阳性和革兰氏阴性细菌引起的医院感染,包括多重耐药病原体感染的一个有前景的候选药物。

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