Stobberingh E E, Houben A W, van Boven C P
J Antimicrob Chemother. 1986 Sep;18(3):345-50. doi: 10.1093/jac/18.3.345.
The in-vitro antibacterial activity of carumonam (Ro 17-2301) was assessed and compared with those of aztreonam and other beta-lactam antibiotics. Carumonam was highly active against the Enterobacteriaceae and Pseudomonas strains resistant to ampicillin (MIC greater than or equal to 256 mg/l) and carbenicillin (MIC greater than or equal to 64 mg/l), respectively. The MICs of carumonam for 90% of the strains ranged between 0.25 mg/l for Klebsiella spp. to 32 mg/l for Pseudomonas spp. The antibacterial activity was minimally altered by changes of medium or inoculum size. Carumonam was resistant to hydrolysis by the plasmid-mediated and chromosomal beta-lactamases tested. Also in the microbiological assay no inactivation was observed. Carumonam was an effective inhibitor of the SHV enzyme and the chromosomal beta-lactamases tested. Against the other plasmid-mediated enzymes carumonam was not an effective inhibitor.
评估了卡芦莫南(Ro 17-2301)的体外抗菌活性,并与氨曲南及其他β-内酰胺类抗生素进行了比较。卡芦莫南对分别耐氨苄西林(MIC大于或等于256mg/L)和羧苄西林(MIC大于或等于64mg/L)的肠杆菌科细菌和铜绿假单胞菌菌株具有高度活性。卡芦莫南对90%菌株的MIC范围为,肺炎克雷伯菌属为0.25mg/L至铜绿假单胞菌属为32mg/L。培养基或接种量的变化对其抗菌活性影响极小。卡芦莫南对所测试的质粒介导和染色体β-内酰胺酶的水解具有抗性。在微生物学测定中也未观察到失活现象。卡芦莫南是所测试的SHV酶和染色体β-内酰胺酶的有效抑制剂。对于其他质粒介导的酶,卡芦莫南不是有效抑制剂。