新型口服头孢菌素头孢布烯(7432-S, SCH 39720)的体外评价。

R N Jones, A L Barry
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引用次数: 0

摘要

7432-S (SCH 39720)是对肠杆菌科细菌最有效的β -内酰胺,对小于或等于8.0微克/ml的菌株的抑制率为92%,而头孢克肟、头孢呋辛和头孢克洛对菌株的抑制率分别为82%、65%和39%。7432-S对流感嗜血杆菌(MIC90,小于或等于0.25微克/毫升)、卡他氏Branhamella (MIC90, 4.0微克/毫升)和脑膜炎奈瑟菌(MIC90,小于或等于0.25微克/毫升)也非常有效。血清B组链球菌和耐青霉素肺炎球菌对7432-S和对照头孢菌的敏感性普遍低于化脓性链球菌和青霉素敏感肺炎链球菌。假单胞菌、肠球菌、不动杆菌和葡萄球菌对7432-S常规耐药(mic50≥32微克/毫升)。
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In vitro evaluation of ceftibuten (7432-S, SCH 39720), a novel orally administered cephalosporin.

7432-S (SCH 39720) was the most active beta-lactam tested against the Enterobacteriaceae, inhibiting 92% of strains at less than or equal to 8.0 micrograms/ml compared to 82%, 65% and 39% of strains inhibited by cefixime, cefuroxime and cefaclor, respectively. 7432-S was also very effective against Haemophilus influenzae (MIC90, less than or equal to 0.25 microgram/ml), Branhamella catarrhalis (MIC90, 4.0 micrograms/ml) and Neisseria meningitidis (MIC90, less than or equal to 0.25 microgram/ml). Serogroup B streptococci and the penicillin-resistant pneumococci were generally less susceptible to 7432-S and comparison cephems than Streptococcus pyogenes or penicillin-susceptible S. pneumoniae isolates. Pseudomonas spp., enterococci, Acinetobacter spp. and Staphylococcus spp. were routinely resistant to 7432-S (MIC50s, greater than or equal to 32 micrograms/ml).

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