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Sch 20569和阿米卡星对庆大霉素敏感及耐药菌的杀菌效力

Bactericidal efficacy of Sch 20569 and amikacin against gentamicin-sensitive and -resistant organisms.

作者信息

Rahal J J, Simberkoff M S, Kagan K, Moldover N H

出版信息

Antimicrob Agents Chemother. 1976 Apr;9(4):595-9. doi: 10.1128/AAC.9.4.595.

Abstract

Sch 20569 is a semisynthetic derivative of gentamicin with activity against many gentamicin-resistant gram-negative bacilli. We compared its bactericidal action with that of gentamicin and amikacin against 171 clinical isolates of Enterobacteriaceae, Staphylococcus aureus, and Pseudomonas aeruginosa. Sch 20569 and amikacin showed markedly greater activity than gentamicin against Escherichia coli, Klebsiella, Enterobacter, Citrobacter, and indole-positive Proteus, primarily by virtue of their lethal effect on gentamicin-resistant strains (minimal bactericidal concentration >/= 12.5 mug/ml). Indole-negative Proteus isolates were uniformly sensitive to Sch 20569, whereas several were resistant to both gentamicin and amikacin. Amikacin was most active against Providencia, as was gentamicin against Serratia. All three agents exhibited similar activity against Pseudomonas. Staphylococcus aureus was more sensitive to gentamicin and Sch 20569 than to amikacin.

摘要

Sch 20569是庆大霉素的半合成衍生物,对许多耐庆大霉素的革兰氏阴性杆菌具有活性。我们比较了它与庆大霉素和阿米卡星对171株临床分离的肠杆菌科细菌、金黄色葡萄球菌和铜绿假单胞菌的杀菌作用。Sch 20569和阿米卡星对大肠杆菌、克雷伯菌属、肠杆菌属、柠檬酸杆菌属和吲哚阳性变形杆菌的活性明显高于庆大霉素,主要是因为它们对耐庆大霉素菌株具有致死作用(最低杀菌浓度≥12.5μg/ml)。吲哚阴性变形杆菌分离株对Sch 20569均敏感,而有几株对庆大霉素和阿米卡星均耐药。阿米卡星对普罗威登斯菌最具活性,庆大霉素对沙雷菌最具活性。这三种药物对铜绿假单胞菌均表现出相似的活性。金黄色葡萄球菌对庆大霉素和Sch 20569比对阿米卡星更敏感。

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Clinical pharmacology of netilmicin.奈替米星的临床药理学
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