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In Vitro Activity of Sch 21420, Derivative of Gentamicin B, Compared to That of Amikacin

机译:与阿米卡星相比,庆大霉素B衍生物Sch 21420的体外活性

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摘要

The minimal inhibitory concentration of Sch-21420 closely paralleled amikacin for 125 strains of aerobic gram-negative bacilli and Staphylococcus aureus primarily selected for testing because of resistance to other aminoglycoside antibiotics. Fifteen of 26 strains requiring 20 μg or more of amikacin per ml for inhibition were inhibited by two- to fourfold less Sch 21420. The majority of organisms resistant to both agents owed their resistance to mechanisms other than the carriage of aminoglycoside-modifying enzymes. Most strains carrying aminoglycoside 6′-acetyltransferase, capable of modifying amikacin, were susceptible to 10 μg or less of Sch 21420 per ml.
机译:Sch-21420的最小抑菌浓度与阿米卡星对125株好氧革兰氏阴性杆菌和金黄色葡萄球菌的抑制作用最接近,主要是因为对其他氨基糖苷类抗生素的耐药性而选择进行测试。需要抑制的每毫升20μg或更大的丁胺卡那霉素的26株菌株中有15株被Sch 21420抑制了2到4倍。大多数对这两种药物都有抗性的生物都对除携带氨基糖苷修饰酶以外的其他机制产生了抗性。大多数携带能够修饰丁胺卡那霉素的氨基糖苷6'-乙酰基转移酶的菌株对每毫升10 21 g或更少的Sch 21420敏感。

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