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使用新型氨基糖苷类抗生素UK-18,892进行的体外研究。

In vitro studies with UK-18,892, a new aminoglycoside antibiotic.

作者信息

Jevons S, Cheeseman H E, Brammer K W

出版信息

Antimicrob Agents Chemother. 1978 Sep;14(3):277-80. doi: 10.1128/AAC.14.3.277.

Abstract

The antibacterial activity of UK-18,892, a new semisynthetic aminoglycoside, was examined against aminoglycoside-susceptible and aminoglycoside-resistant clinical isolates of gram-negative bacilli and Staphylococcus aureus. UK-18,892 had a similar degree of activity to those of amikacin and kanamycin A against aminoglycoside-susceptible bacteria but was less potent than gentamicin against all isolates except Providencia spp. UK-18,892 was highly active against aminoglycoside-resistant bacteria, inhibiting 93% of the 268 isolates examined at 12.5 mug/ml. Amikacin was similarly active, whereas gentamicin inhibited only 14% of these isolates at 12.5 mug/ml.

摘要

对新型半合成氨基糖苷类药物UK-18,892针对氨基糖苷类敏感和耐药的革兰氏阴性杆菌及金黄色葡萄球菌临床分离株的抗菌活性进行了检测。UK-18,892对氨基糖苷类敏感菌的活性程度与阿米卡星和卡那霉素A相似,但除普罗威登斯菌属外,对所有分离株的效力均低于庆大霉素。UK-18,892对氨基糖苷类耐药菌具有高度活性,在12.5μg/ml浓度下可抑制所检测的268株分离株中的93%。阿米卡星也具有类似活性,而庆大霉素在12.5μg/ml浓度下仅能抑制这些分离株中的14%。

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本文引用的文献

2
Phosphorylation and inactivation of kanamycin by Pseudomonas aeruginosa.
J Antibiot (Tokyo). 1968 Feb;21(2):154-5. doi: 10.7164/antibiotics.21.154.
6
The mechanisms of resistance to aminoglycosides in the genus Pseudomonas.
J Antimicrob Chemother. 1978 Mar;4(2):121-9. doi: 10.1093/jac/4.2.121.
7
Synthesis and antibacterial activities of 1-N [(S)-omega-amino-2-hydroxyalkyl] kanamycin A derivatives.
J Antibiot (Tokyo). 1977 Oct;30(10):843-6. doi: 10.7164/antibiotics.30.843.
9
Controlled comparison of amikacin and gentamicin.阿米卡星与庆大霉素的对照比较。
N Engl J Med. 1977 Feb 17;296(7):349-53. doi: 10.1056/NEJM197702172960701.
10
Amikacin.
Lancet. 1977 Sep 24;2(8039):659-60. doi: 10.1016/s0140-6736(77)92523-5.

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