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庆大霉素与β-内酰胺类抗生素联合作用对铜绿假单胞菌的体外实验(作者译)

[In vitro experiments on the working of combinations of gentamicin and beta-lactam antibiotics against Pseudonomas aeruginosa (author's transl)].

作者信息

Ullmann U

出版信息

Immun Infekt. 1975 Apr;3(2):79-85.

PMID:810407
Abstract

The M.B.C.'s of gentamicin and carbenicillin against Pseudonomas aeruginosa NCTC 10490 were measured under controlled conditions using a Biophotometer. The M.B.C. of gentamicin was 15 mug/ml but even in a concentration of 1,000 mug/ml carbenicillin was not bactericidal. In further experiments, subinhibitory concentrations of gentamicin (1 mug/ml) together with varying concentrations of carbenicillin were added to a log phase culture of the organism. Under these conditions the M.B.C. of carbenicillin was now 6 mug/ml. In tube dilution test the M.B.C. of carbenicillin alone was 15.6 mug/ml and for gentamicin 3.9 mug/ml. The M.B.C.'s of other beta-lactam antibiotics (ampicillin, penicillin G and cephalothin) were four to five times as great as for carbenicillin whereas that for ticarcillin was identical. Parallel to the "multiplication inhibition" test in the Biophotometer we investigated 51 strains of Pseudomonas aeruginosa freshly isolated from clinical material. Their M.B.C.'s were determined in tube dilution tests against doubling dilutions of beta-lactam antibiotics, with and without the addition of 1 mug/ml gentamicin. With this concentration of gentamicin, the M.B.C.'s of carbenicillin and ticarcillin were considerably lower than for these substances alone. In comparison to carbenicillin, ticarcillin was more effective against Pseudomonas aeruginosa. Our findings indicate that for Pseudomonas aeruginosa infections the combination of gentamicin with other beta-lactam antibiotics (ampicillin, penicillin G and cephalothin) is to be avoided. But the combination of gentamicin with either carbenicillin or ticarcillin appeared to be effective.

摘要

在可控条件下,使用生物光度计测定庆大霉素和羧苄西林对铜绿假单胞菌NCTC 10490的最低杀菌浓度(M.B.C.)。庆大霉素的M.B.C.为15微克/毫升,但即使在1000微克/毫升的浓度下,羧苄西林也没有杀菌作用。在进一步的实验中,将亚抑菌浓度的庆大霉素(1微克/毫升)与不同浓度的羧苄西林添加到该菌的对数期培养物中。在这些条件下,羧苄西林的M.B.C.现在为6微克/毫升。在试管稀释试验中,单独羧苄西林的M.B.C.为15.6微克/毫升,庆大霉素为3.9微克/毫升。其他β-内酰胺抗生素(氨苄西林、青霉素G和头孢噻吩)的M.B.C.是羧苄西林的四到五倍,而替卡西林的M.B.C.与羧苄西林相同。与生物光度计中的“增殖抑制”试验平行,我们研究了从临床材料中新鲜分离的51株铜绿假单胞菌。在试管稀释试验中,针对β-内酰胺抗生素的双倍稀释液,测定它们在添加和不添加1微克/毫升庆大霉素情况下的M.B.C.。在此庆大霉素浓度下,羧苄西林和替卡西林的M.B.C.明显低于单独使用这些物质时。与羧苄西林相比,替卡西林对铜绿假单胞菌更有效。我们的研究结果表明,对于铜绿假单胞菌感染,应避免庆大霉素与其他β-内酰胺抗生素(氨苄西林、青霉素G和头孢噻吩)联合使用。但庆大霉素与羧苄西林或替卡西林联合使用似乎是有效的。

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