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HR756与头孢噻吩、头孢西丁和头孢孟多的体外活性比较。

Comparison of the in vitro activities of HR756 with cephalothin, cefoxitin, and cefamandole.

作者信息

Sosna J P, Murray P R, Medoff G

出版信息

Antimicrob Agents Chemother. 1978 Dec;14(6):876-9. doi: 10.1128/AAC.14.6.876.

Abstract

The in vitro activity of HR756, a new semisynthetic cephalosporin, was compared with the activities of cephalothin, cefoxitin, and cefamandole against 1,535 isolates of gram-positive and gram-negative bacteria. HR756 was less active than cephalothin and cefamandole and twofold more active than cefoxitin against Staphylococcus. All four of the antibiotics were inactive against the enterococcus group of Streptococcus; however, HR756 was the most active antibiotic against the other isolates of Streptococcus. HR756 was also more active against isolates of Enterobacteriaceae, including 84 to 95% of the isolates resistant to one or more of the other three antibiotics. HR756, at a concentration of 12.5 mug/ml, inhibited 86, 75, and 100% of the isolates of Pseudomonas aeruginosa, other Pseudomonas species, and Acinetobacter, respectively. The minimal inhibitory concentrations and minimal bactericidal concentrations of HR756 were within one twofold dilution for 11 of 21 gram-positive cocci and 119 of 125 gram-negative bacilli tested.

摘要

将一种新型半合成头孢菌素HR756的体外活性与头孢噻吩、头孢西丁和头孢孟多对1535株革兰氏阳性和革兰氏阴性菌的活性进行了比较。HR756对葡萄球菌的活性低于头孢噻吩和头孢孟多,比头孢西丁高两倍。这四种抗生素对链球菌属肠球菌均无活性;然而,HR756是对其他链球菌分离株活性最强的抗生素。HR756对肠杆菌科分离株也更具活性,包括84%至95%对其他三种抗生素中的一种或多种耐药的分离株。在浓度为12.5μg/ml时,HR756分别抑制了86%、75%和100%的铜绿假单胞菌、其他假单胞菌属和不动杆菌属分离株。在测试的21株革兰氏阳性球菌中的11株和125株革兰氏阴性杆菌中的119株中,HR756的最低抑菌浓度和最低杀菌浓度在一个两倍稀释范围内。

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