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新型青霉烯类抗生素FCE 22101与其他β-内酰胺类抗生素的体外活性比较。

The in-vitro activity of a novel penem FCE 22101 compared to other beta-lactam antibiotics.

作者信息

Neu H C, Chin N X, Labthavikul P

出版信息

J Antimicrob Chemother. 1985 Sep;16(3):305-13. doi: 10.1093/jac/16.3.305.

Abstract

FCE 22101 is a penem antibiotic which inhibits the majority of Enterobacteriaceae, Haemophilus influenzae, and Neisseria gonorrhoeae at concentrations of 0.5-4 mg/l. It inhibits staphylococci, haemolytic streptococci and Streptococcus pneumoniae at less than or equal to 0.25 mg/l. Pseudomonas aeruginosa and other Pseudomonas species are resistant. Bacteroides fragilis and Clostridium species are inhibited by less than or equal to 1 mg/l. FCE 22101 is not hydrolyzed by the common plasmid and chrosmosomal beta-lactamases. It shows minimal discrepancy between MIC and MBC values and there is minimal effect of inoculum size. Although FCE 22101 is generally less active against Enterobacteriaceae than are cefotaxime and ceftazidime, it does inhibit some Enterobacter spp. resistant to these agents. FCE 22101 and imipenem are similar in activity against Gram-positive and anaerobic species.

摘要

FCE 22101是一种青霉烯类抗生素,在浓度为0.5 - 4毫克/升时可抑制大多数肠杆菌科细菌、流感嗜血杆菌和淋病奈瑟菌。在小于或等于0.25毫克/升时可抑制葡萄球菌、溶血性链球菌和肺炎链球菌。铜绿假单胞菌和其他假单胞菌属具有耐药性。脆弱拟杆菌和梭菌属在小于或等于1毫克/升时受到抑制。FCE 22101不会被常见的质粒和染色体β-内酰胺酶水解。其最低抑菌浓度(MIC)和最低杀菌浓度(MBC)值之间差异极小,接种量大小的影响也极小。尽管FCE 22101对肠杆菌科细菌的活性通常低于头孢噻肟和头孢他啶,但它确实能抑制一些对这些药物耐药的肠杆菌属细菌。FCE 22101和亚胺培南对革兰氏阳性菌和厌氧菌的活性相似。

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