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阿米卡星、庆大霉素和卡那霉素对铜绿假单胞菌的活性。

Activity of amikacin, gentamicin and kanamycin against Pseudomonas aeruginosa.

作者信息

Ximenes J, Bassoi O N, de Menezes J P, Fry W

出版信息

J Int Med Res. 1976;4(3):165-75. doi: 10.1177/030006057600400304.

Abstract

The activity of amikacin, gentamicin and kanamycin was tested in vitro against clinical isolates of Pseudomonas aeruginosa. Concentrations of the antibiotics in serum and in saline solution were prepared according to serum levels produced in volunteers 15 minutes, 1,2, and 6 hours after a single intramuscular injection of 500 mg amikacin, 80 mg gentamicin and 500 mg kanamycin. Following isolation of the Pseudomonas strains in cultures, they were incubated and seeded in Mueller-Hinton broth, then 10(-7) dilutions of the organisms were kept in contact with the prepared antibiotic solutions in serum and in saline solution for three hours, the approximate half-life of the antibiotics in serum. Amikacin was active at concentrations seen six hours post-dose, inhibiting growth in a total of 72-5% of seeded plates. Gentamicin was active for only two hours and inhibited growth in 2-5% of the plates. Kanamycin showed no antipseudomonal activity.

摘要

对阿米卡星、庆大霉素和卡那霉素针对铜绿假单胞菌临床分离株的活性进行了体外测试。根据单次肌内注射500mg阿米卡星、80mg庆大霉素和500mg卡那霉素后15分钟、1小时、2小时和6小时志愿者体内产生的血清水平,制备血清和盐溶液中抗生素的浓度。在培养物中分离出假单胞菌菌株后,将它们在穆勒-欣顿肉汤中孵育并接种,然后将10(-7)倍稀释的菌株与血清和盐溶液中制备好的抗生素溶液接触3小时,这大约是抗生素在血清中的半衰期。阿米卡星在给药后6小时的浓度下具有活性,抑制了总共72.5%接种平板上的生长。庆大霉素仅在两小时内具有活性,抑制了2.5%平板上的生长。卡那霉素未显示出抗假单胞菌活性。

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