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新型抗假单胞菌广谱青霉素Bay k 4999和哌拉西林与其他β-内酰胺类药物的体外活性比较。

Comparison of the in vitro activity of Bay k 4999 and piperacillin, two new antipseudomonal broad-spectrum penicillins, with other beta-lactam drugs.

作者信息

Wise R, Andrews J M, Bedford K A

出版信息

Antimicrob Agents Chemother. 1978 Oct;14(4):549-52. doi: 10.1128/AAC.14.4.549.

Abstract

Bay k 4999 and piperacillin, two new substituted ampicillins, were compared with other beta-lactam antibiotics, including carbenicillin, azlocillin, mezlocillin, benzylpenicillin, ampicillin, and cefoxitin, against a wide range of gram-positive and -negative organisms. Bay k 4999 and piperacillin were extremely active against Pseudomonas aeruginosa (50% inhibited by 2 mug/ml), being about 16-fold more active than carbenicillin. Bay k 4999 was the most active drug against Escherichia coli (50% inhibited by 0.5 mug/ml) and Klebsiella spp. (50% inhibited by 2 mug/ml). Piperacillin and Bay k 4999 were equally active against Proteus spp., and piperacillin had high activity against Bacteroides fragilis (50% inhibited by between 1 and 2 mug/ml).

摘要

将新型取代氨苄西林Bay k 4999和哌拉西林与其他β-内酰胺类抗生素(包括羧苄西林、阿洛西林、美洛西林、苄青霉素、氨苄西林和头孢西丁)进行比较,以对抗多种革兰氏阳性和阴性菌。Bay k 4999和哌拉西林对铜绿假单胞菌具有极强的活性(2微克/毫升可抑制50%),其活性约为羧苄西林的16倍。Bay k 4999是对大肠杆菌(0.5微克/毫升可抑制50%)和克雷伯菌属(2微克/毫升可抑制50%)活性最强的药物。哌拉西林和Bay k 4999对变形杆菌属的活性相当,哌拉西林对脆弱拟杆菌具有高活性(1至2微克/毫升可抑制50%)。

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BL-P1654: a bacteriostatic penicillin?BL-P1654:一种抑菌性青霉素?
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