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核糖霉素、庆大霉素、氨苄青霉素和林可霉素的体外及体内抗菌活性比较

Comparative antimicrobial activities of ribostamycin, gentamicin, ampicillin and lincomycin in vitro and in vivo.

作者信息

Inouye S, Watanabe T, Kitasato I

机构信息

Central Research Laboratory, Meiji Seika Kaisha, Ltd., Yokohama, Japan.

出版信息

Drugs Exp Clin Res. 1989;15(10):465-76.

PMID:2632215
Abstract

The antimicrobial activity of ribostamycin, a unique aminoglycoside antibiotic possessing a neutral sugar component, was compared with those of gentamicin, ampicillin and lincomycin in vitro and in vivo. Ribostamycin showed comparable or slightly weaker in vitro activity than the reference antibiotics against Gram-positive bacteria. Against Gram-negative bacteria, ribostamycin was less active than gentamicin, but comparable to or more active than ampicillin. Lincomycin was less active or inactive to Gram-negative bacteria. Ribostamycin was active against some gentamicin-resistant bacteria, especially K. pneumoniae possessing the aminoglycoside-modifying enzymes AAC(3)-l and AAD(2"). The in vivo activity of ribostamycin was weaker than that of gentamicin, but comparable to that of ampicillin and lincomycin against Gram-positive bacteria, and superior to that of ampicillin against Gram-negative bacteria. The in vivo activity of ribostamycin was characterized by (i) and ED50 value not so affected by the challenge inoculum as that of ampicillin; (ii) a lower ED50 value by bolus administration than that by divided administration of the same dosage; and (iii) a lower ED50 value than that expected from the MIC value as compared with that of ampicillin and lincomycin. These characteristics are explained by the rapid and potent bactericidal activity of ribostamycin at high inoculum and high drug concentration, assisted by high serum concentration in mice.

摘要

核糖霉素是一种具有中性糖成分的独特氨基糖苷类抗生素,对其抗菌活性在体外和体内与庆大霉素、氨苄西林和林可霉素进行了比较。核糖霉素对革兰氏阳性菌的体外活性与参考抗生素相当或略弱。对革兰氏阴性菌,核糖霉素的活性低于庆大霉素,但与氨苄西林相当或高于氨苄西林。林可霉素对革兰氏阴性菌活性较弱或无活性。核糖霉素对一些耐庆大霉素的细菌有活性,特别是对具有氨基糖苷修饰酶AAC(3)-I和AAD(2")的肺炎克雷伯菌。核糖霉素的体内活性比庆大霉素弱,但对革兰氏阳性菌与氨苄西林和林可霉素相当,对革兰氏阴性菌优于氨苄西林。核糖霉素的体内活性特点为:(i) ED50值不像氨苄西林那样受接种量影响;(ii) 大剂量给药时的ED50值低于相同剂量分次给药时的ED50值;(iii) 与氨苄西林和林可霉素相比,其ED50值低于根据MIC值预期的值。这些特点可通过核糖霉素在高接种量和高药物浓度时的快速强效杀菌活性来解释,小鼠体内高血清浓度对此有辅助作用。

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