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头孢他啶:体外比较研究。

Ceftazidime: comparative in-vitro study.

作者信息

Verbist L, Verhaegen J

机构信息

Diagnostic Microbiology Laboratory, St Rafaël Hospital, University of Leuven, B-3000 Leuven, Belgium.

出版信息

J Antimicrob Chemother. 1981 Sep;8 Suppl B:67-71. doi: 10.1093/jac/8.suppl_b.67.

Abstract

Ceftazidime showed moderate activity against Staphylococcus aureus and a high activity against Haemophilus influenzae and the streptococci except against the enterococci. Ceftazidime inhibited 90% of the 830 Enterobacteriaceae tested at a concentration of 0.5 mg/l and 99% at 8 mg/l, an activity very similar to that of cefotaxime. Against Pseudomonas spp. ceftazidime proved to be the most active beta-lactam antibiotic studied. It inhibited 67% of the 141 Ps. aeruginosa strains at 2 mg/l, 84% at 4 mg/l, 98% at 8 mg/l and 100% at 16 mg/l. The inhibitory and the bactericidal concentrations were very close and there was only a minor effect of the inoculum. Ceftazidime retained its high activity against microorganisms with acquired as well as with natural resistance to other beta-lactam antibiotics.

摘要

头孢他啶对金黄色葡萄球菌显示出中度活性,对流感嗜血杆菌和链球菌(除肠球菌外)具有高活性。头孢他啶在浓度为0.5mg/l时抑制了所测试的830株肠杆菌科细菌中的90%,在8mg/l时抑制了99%,其活性与头孢噻肟非常相似。对于假单胞菌属,头孢他啶被证明是所研究的最具活性的β-内酰胺抗生素。它在2mg/l时抑制了141株铜绿假单胞菌菌株中的67%,在4mg/l时抑制了84%,在8mg/l时抑制了98%,在16mg/l时抑制了100%。抑菌浓度和杀菌浓度非常接近,接种量的影响很小。头孢他啶对获得性以及对其他β-内酰胺抗生素具有天然耐药性的微生物仍保持高活性。

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