Del Bene V E, Farrar W E
Antimicrob Agents Chemother. 1972 Apr;1(4):340-2. doi: 10.1128/AAC.1.4.340.
The in vitro activity of the aminoglycoside antibiotic tobramycin was demonstrated by broth dilution and single-disc methods on 50 isolates each of Staphylococcus aureus, Klebsiella or Enterobacter, indole-positive and -negative Proteus, Escherichia coli, and Pseudomonas aeruginosa. All organisms were inhibited by 6.25 mug or less of the drug/ml. Pseudomonas strains resistant to kanamycin or gentamicin or both were susceptible to tobramycin. Those strains which were inhibited by 6.25 mug of tobramycin/ml by the broth dilution method had zone diameters of 16 mm or more by the single-disc method. Of 313 organisms tested by the disc method, 3 strains were found to be resistant to tobramycin, 73 were resistant to kanamycin, and 18 were resistant to gentamicin. Tobramycin was found to have satisfactory in vitro activity against many clinically important organisms, including strains resistant to gentamicin and kanamycin.
采用肉汤稀释法和单纸片法,对50株金黄色葡萄球菌、克雷伯菌或肠杆菌、吲哚阳性和阴性变形杆菌、大肠杆菌及铜绿假单胞菌进行了氨基糖苷类抗生素妥布霉素的体外活性研究。所有菌株均被6.25μg/ml或更低浓度的药物所抑制。对卡那霉素或庆大霉素或两者耐药的铜绿假单胞菌菌株对妥布霉素敏感。通过肉汤稀释法被6.25μg/ml妥布霉素抑制的菌株,用单纸片法测定其抑菌圈直径为16mm或更大。在用纸片法检测的313株菌株中,发现3株对妥布霉素耐药,73株对卡那霉素耐药,18株对庆大霉素耐药。结果表明,妥布霉素对许多临床重要菌株具有良好的体外活性,包括对庆大霉素和卡那霉素耐药的菌株。