Riff L J, Thomason J L
J Antibiot (Tokyo). 1982 Jul;35(7):850-7. doi: 10.7164/antibiotics.35.850.
Gentamicin, tobramycin, netilmicin, kanamycin and amikacin were evaluated over time for biologic activity in human serum, in combination with 6 beta-lactams. Simple addition of aminoglycoside and 250 micrograms/ml penicillin produced aminoglycoside inactivation at 8 approximately 48 hours. However, all beta-lactam antibiotics exhibited decay in human serum at 37 degrees C, even when present as a single component. All aminoglycosides could be inactivated by penicillins but differed markedly in their susceptibility. Amikacin, at 20 micrograms/ml, was the least inactivated by any penicillin; netilmicin, at 10 micrograms/ml, was the next least inactivated. Tobramycin had pronounced loss of biological activity exceeding that of any aminoglycoside, appearing as early as 8 hours. The ability of the various penicillins to produce aminoglycoside inactivation, in approximate descending order, was; carbenicillin, ticarcillin, penicillin G, oxacillin, methicillin, ampicillin. Cephalothin produced minimal inactivation. Aminoglycoside inactivation also occurred at 25 degrees C, and with many samples stored at 4 degrees C, although at proportionately slower rates. For samples stored at -20 degrees C, only tobramycin had substantial loss of activity. These data indicate that adequate handling and prompt assay of the specimen are important.
对庆大霉素、妥布霉素、奈替米星、卡那霉素和阿米卡星与6种β-内酰胺类药物联合使用时在人血清中的生物活性随时间进行了评估。简单地将氨基糖苷类药物与250微克/毫升青霉素混合,在8至48小时内会导致氨基糖苷类药物失活。然而,所有β-内酰胺类抗生素在37℃的人血清中都会降解,即使作为单一成分存在时也是如此。所有氨基糖苷类药物都可被青霉素灭活,但它们的敏感性差异显著。20微克/毫升的阿米卡星被任何青霉素灭活的程度最低;10微克/毫升的奈替米星其次。妥布霉素的生物活性明显丧失,超过任何氨基糖苷类药物,早在8小时就出现。各种青霉素导致氨基糖苷类药物失活的能力,按大致降序排列为:羧苄西林、替卡西林、青霉素G、苯唑西林、甲氧西林、氨苄西林。头孢噻吩产生的失活作用最小。在25℃时也会发生氨基糖苷类药物失活,许多储存在4℃的样品也是如此,不过失活速率相对较慢。对于储存在-20℃的样品,只有妥布霉素有大量活性丧失。这些数据表明,对标本进行妥善处理和及时检测很重要。