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In Vitro Studies of Netilmicin, a New Aminoglycoside Antibiotic

机译:新型氨基糖甙类抗生素奈替米星的体外研究

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摘要

Netilmicin, a semisynthetic derivative of sisomicin, was tested in vitro against 600 clinical bacterial isolates. At a concentration of 1.56 μg/ml, over 90% of gram-negative bacilli were inhibited. Netilmicin was substantially more active against isolates of Serratia marcescens and Enterobacter spp. than gentamicin, sisomicin, tobramycin, or amikacin. Isolates of Staphylococcus aureus (both penicillin G susceptible and resistant) were quite susceptible to netilmicin. Most isolates of Klebsiella spp. and Serratia spp. and some of the isolates of Pseudomonas aeruginosa that were resistant to gentamicin proved to be susceptible to netilmicin.
机译:Netilmicin是sisomicin的半合成衍生物,已针对600种临床细菌分离株进行了体外测试。在1.56μg/ ml的浓度下,超过90%的革兰氏阴性杆菌被抑制。耐尼替米星对粘质沙雷氏菌和肠杆菌属的分离物更具活性。比庆大霉素,西索霉素,妥布霉素或丁胺卡那霉素高。金黄色葡萄球菌的分离株(青霉素G易感和耐药)对奈替米星相当敏感。克雷伯菌属的大多数分离株。和沙雷氏菌以及一些对庆大霉素有抗药性的铜绿假单胞菌分离株被证明对奈替米星敏感。

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