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头孢替坦:体外活性概况。

Cefotetan: profile of in-vitro activity.

作者信息

Bauernfeind A

出版信息

J Antimicrob Chemother. 1983 Jan;11 Suppl:19-29. doi: 10.1093/jac/11.suppl_a.19.

Abstract

Cefotetan, a novel 7 alpha-methoxy cephalosporin, was shown to be comparable to other third-generation cephalosporins when tested in vitro against 1063 Gram-negative clinical isolates of 11 species. Ninety per cent of all isolates of Escherichia coli, Klebsiella, Proteus mirabilis, Proteus vulgaris, Proteus rettgeri, Providencia stuartii, Serratia marcescens and Citrobacter freundii were inhibited by concentrations of cefotetan between 0.07 and 3.2 mg/l. Activity against Gram-positive cocci was about equal to that of moxalactam. Pseudomonas aeruginosa and Acinetobacter were resistant. Cefotetan inhibited about two-thirds of Enterobacter strains at 16 mg/l. beta-Lactamases of Enterobacter cloacae highly resistant to cefotetan inactivated this cephamycin. These strains were resistant to most other beta-lactams as well. Synergism between cefotetan and aminoglycosides was found in 8 out of 16 Gram-negatives.

摘要

头孢替坦是一种新型的7α-甲氧基头孢菌素,在体外对11种革兰氏阴性临床分离菌的1063株菌株进行测试时,其表现与其他第三代头孢菌素相当。在所有大肠杆菌、克雷伯菌、奇异变形杆菌、普通变形杆菌、雷氏变形杆菌、斯氏普罗威登斯菌、粘质沙雷氏菌和弗氏柠檬酸杆菌分离株中,90%在头孢替坦浓度为0.07至3.2mg/l时受到抑制。对革兰氏阳性球菌的活性约等于莫拉司亭。铜绿假单胞菌和不动杆菌具有耐药性。头孢替坦在16mg/l时可抑制约三分之二的肠杆菌菌株。对头孢替坦高度耐药的阴沟肠杆菌β-内酰胺酶可使这种头霉素失活。这些菌株对大多数其他β-内酰胺类药物也具有耐药性。在16株革兰氏阴性菌中,有8株发现头孢替坦与氨基糖苷类药物之间存在协同作用。

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