Shannon K, King A, Warren C, Phillips I
Antimicrob Agents Chemother. 1980 Aug;18(2):292-8. doi: 10.1128/AAC.18.2.292.
The in vitro activity of Ro 13-9904 was assessed against clinical isolated of common bacteria. Its activity against most enterobacteria was similar to that of cefotaxime and moxalactam, but it was even more active than these compounds against all Proteus species. It was also highly active against Haemophilus influenzae and Neisseria gonorrhoeae, including beta-lactamase producers. Like cefotaxime and moxalactam, Or 13-9904 was approximately eightfold more active than carbenicillin against most isolates of Pseudomonas aeruginosa and also active against highly carbenicillin-resistant isolates, but it was relatively inactive against moderately carbenicillin-resistant isolates. Ro 13-9904 also resembled cefotaxime and moxalactam in that it was active, though less so than cephaloridine, against staphylococci and streptococci, except for methicillin-resistant staphylococci and Streptococcus faecalis, which were resistant to it. It was less active than cefoxitin but slightly more active than ampicillin against both Bacteroides fragilis and other Bacteroides spp. Ro 13-9904 was resistant to most beta-lactamases but was attacked by enzymes from B. fragilis, isolates of indole-positive Proteus species, and also by a cefoxitin-hydrolyzing enzyme from an isolate of Enterobacter cloacae.
对Ro 13-9904针对常见细菌临床分离株的体外活性进行了评估。它对大多数肠杆菌科细菌的活性与头孢噻肟和莫西拉坦相似,但对所有变形杆菌属细菌的活性比这些化合物更强。它对流感嗜血杆菌和淋病奈瑟菌也具有高活性,包括产β-内酰胺酶的菌株。与头孢噻肟和莫西拉坦一样,Ro 13-9904对大多数铜绿假单胞菌分离株的活性比对羧苄西林高约八倍,并且对高度耐羧苄西林的分离株也有活性,但对中度耐羧苄西林的分离株相对无活性。Ro 13-9904在对葡萄球菌和链球菌(耐甲氧西林葡萄球菌和粪肠球菌除外,它们对其耐药)有活性方面也与头孢噻肟和莫西拉坦相似,不过活性比头孢利定低。它对脆弱拟杆菌和其他拟杆菌属细菌的活性比头孢西丁低,但比对氨苄西林略高。Ro 13-9904对大多数β-内酰胺酶耐药,但易被脆弱拟杆菌、吲哚阳性变形杆菌属分离株产生的酶以及阴沟肠杆菌分离株产生的一种水解头孢西丁的酶所攻击。