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新型头孢菌素头孢呋辛对革兰氏阴性菌的溶菌活性。

Lytic activity of a new cephalosporin, cefuroxime, against gram-negative bacteria.

作者信息

Russell A D, Tottle P C

出版信息

Chemotherapy. 1978;24(6):354-9. doi: 10.1159/000237807.

Abstract

Cefuroxime, a new cephalosporin antibiotic, was inhibitory at low concentrations to several types of gram-negative bacteria. It was considerably more stable than cephaloridine or cephalothin to the beta-lactamases produced by Escherichia coli (RP1), Klebsiella aerogenes K1 and Enterobacter cloacae P99. Concentrations of cefuroxime much greater than the minimum inhibitory concentration (MIC) were usually necessary to induce lysis of beta-lactamase and non-beta-lactamase producers. In contrast, cephaloridine, cephalothin and ampicillin were rapidly bacteriolytic at, or near, the respective MIC against non-beta-lactamase producers, whereas the activity of these three antibiotics was considerably reduced against beta-lactamase-producing strains.

摘要

头孢呋辛是一种新型头孢菌素抗生素,在低浓度时对几种革兰氏阴性菌具有抑制作用。它比头孢噻啶或头孢噻吩对大肠杆菌(RP1)、产气克雷伯菌K1和阴沟肠杆菌P99产生的β-内酰胺酶稳定得多。通常需要远高于最低抑菌浓度(MIC)的头孢呋辛浓度才能诱导β-内酰胺酶产生菌和非β-内酰胺酶产生菌的裂解。相比之下,头孢噻啶、头孢噻吩和氨苄西林在针对非β-内酰胺酶产生菌的各自MIC或接近MIC时能迅速产生溶菌作用,而这三种抗生素对β-内酰胺酶产生菌的活性则大大降低。

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