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新型碳青霉烯类抗生素SF-2103A作为β-内酰胺酶抑制剂的体外评价

In vitro evaluation of SF-2103A, a novel carbapenem antibiotic, as a beta-lactamase inhibitor.

作者信息

Niwa T, Yoshida T, Tamura A, Kazuno Y, Inouye S, Ito T, Kojima M

出版信息

J Antibiot (Tokyo). 1986 Jul;39(7):943-55. doi: 10.7164/antibiotics.39.943.

Abstract

SF-2103A, a new carbapenem antibiotic, exhibited a broad antibacterial spectrum and a potent inhibitory activity against a wide range of beta-lactamases, in particular, against cephalosporinases, with lower I50 values than those displayed by sulbactam and clavulanic acid. Using a fixed combination and checkerboard titration, in vitro synergy against the majority of the beta-lactamase-producing strains tested was demonstrated between SF-2103A and various beta-lactam antibiotics, especially cefotaxime, ceftizoxime, and cefoperazone. The synergistic effect of SF-2103A was more pronounced than that of sulbactam. The in vitro synergy was also confirmed by bactericidal and bacteriolytic activities and morphological effects.

摘要

新型碳青霉烯类抗生素SF - 2103A具有广谱抗菌活性,对多种β - 内酰胺酶,尤其是头孢菌素酶具有强大的抑制活性,其I50值低于舒巴坦和克拉维酸。通过固定组合和棋盘滴定法,证实SF - 2103A与多种β - 内酰胺类抗生素,特别是头孢噻肟、头孢唑肟和头孢哌酮之间,对大多数产β - 内酰胺酶菌株具有体外协同作用。SF - 2103A的协同作用比舒巴坦更显著。杀菌、溶菌活性及形态学效应也证实了其体外协同作用。

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Beta-lactamase inhibitors from laboratory to clinic.从实验室到临床的β-内酰胺酶抑制剂
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