首页> 外文OA文献 >Comparison of in vitro activity of Sch 21420, a gentamicin B derivative, with those of amikacin, gentamicin, netilmicin, sisomicin, and tobramycin.
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Comparison of in vitro activity of Sch 21420, a gentamicin B derivative, with those of amikacin, gentamicin, netilmicin, sisomicin, and tobramycin.

机译:庆大霉素B衍生物Sch 21420与阿米卡星,庆大霉素,奈替米星,西索米星和妥布霉素的体外活性比较。

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摘要

Sch 21420 is a new aminoglycoside synthesized from gentamicin B. Susceptibility tests with Sch 21420, amikacin, gentamicin, netilmicin, sisomicin, and tobramycin were performed on a variety of bacterial species including 44 with known mechanisms of resistance to aminoglycosides. Sch 21420 and amikacin had similar effects on all except Haemophilus influenzae and Neisseria species, which were more susceptible to amikacin. Except with some strains of Serratia marcescens, the drugs used were bactericidal. Sch 21420 and amikacin were more stable than the other four aminoglycosides in the presence of the inactivating enzymes produced by some strains. Strains which were very resistant to Sch 21420 and emikacin either were permeability mutants or produced AAC (6')-I inactivating enzyme. The effect of cations on the susceptibilities of these strains to Sch 21420 and amikacin was seen mostly with Pseudomonas aeruginosa and to Sch 21420 with Acinetobacter. Cations did not affect the susceptibilities of other Pseudomonas species, Enterobacteriaceae, Staphylococcus aureus, or Streptococcus faecalis to Sch 21420 or amikacin.
机译:Sch 21420是一种由庆大霉素B合成的新型氨基糖苷。对Sch细菌(420),阿米卡星,庆大霉素,奈替米星,西索米星和妥布霉素的敏感性试验是在包括44种已知对氨基糖苷耐药机制的多种细菌上进行的。 Sch 21420和丁胺卡那霉素对所有流感病毒嗜血杆菌和奈瑟氏菌均具有相似的作用,它们对丁胺卡那霉素更易感。除某些粘质沙雷氏菌外,其他药物均具有杀菌作用。在某些菌株产生的失活酶存在下,Sch 21420和丁胺卡那霉素比其他四种氨基糖苷更稳定。对Sch 21420和丁胺卡那霉素非常抗性的菌株是通透性突变体或产生了AAC(6')-I灭活酶。阳离子对这些菌株对Sch 21420和丁胺卡那霉素敏感性的影响主要在铜绿假单胞菌和对不动杆菌对Sch 21420的敏感性中看到。阳离子不影响其他假单胞菌种,肠杆菌科,金黄色葡萄球菌或粪链球菌对Sch 21420或丁胺卡那霉素的敏感性。

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