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阿莫西林加克拉维酸对流感嗜血杆菌和卡他莫拉菌的体外活性。

In vitro activity of amoxicillin plus clavulanic acid against Haemophilus influenzae and Branhamella catarrhalis.

作者信息

Liljequist B O, Gezelius L

出版信息

Eur J Clin Microbiol. 1986 Dec;5(6):615-21. doi: 10.1007/BF02013284.

Abstract

The in vitro activity of amoxicillin in the presence of clavulanic acid against clinical isolates of Haemophilus influenzae and Branhamella catarrhalis was assessed in comparison with ampicillin, amoxicillin, cefaclor and erythromycin. The isolates were selected so as to yield equal numbers of beta-lactamase producing and non-beta-lactamase producing strains of the two species. MICs obtained by agar dilution indicated that amoxicillin in the presence of clavulanic acid was the most active of the drugs tested. Clavulanic acid potentiated the activity of amoxicillin against beta-lactamase-producing strains of both Haemophilus influenzae and Branhamella catarrhalis. Further studies on a few strains of each species revealed that the beta-lactamase of Haemophilus influenzae (TEM-1) rapidly inactivated ampicillin and slowly inactivated cefaclor but not cefuroxime. The Branhamella catarrhalis enzyme rapidly inactivated cefaclor, ampicillin and to some extent cefuroxime. Clavulanic acid afforded protection against the beta-lactamase action of both species when beta-lactam antibiotics were added to bacterial cultures.

摘要

评估了阿莫西林与克拉维酸联合使用时对流感嗜血杆菌和卡他布兰汉菌临床分离株的体外活性,并与氨苄西林、阿莫西林、头孢克洛和红霉素进行了比较。所选分离株中,这两个菌种产生β-内酰胺酶和不产生β-内酰胺酶的菌株数量相等。琼脂稀释法测得的最低抑菌浓度表明,阿莫西林与克拉维酸联合使用时是所测试药物中活性最强的。克拉维酸增强了阿莫西林对流感嗜血杆菌和卡他布兰汉菌产β-内酰胺酶菌株的活性。对每个菌种的少数菌株进一步研究发现,流感嗜血杆菌(TEM-1)的β-内酰胺酶能迅速使氨苄西林失活,缓慢使头孢克洛失活,但不会使头孢呋辛失活。卡他布兰汉菌的酶能迅速使头孢克洛、氨苄西林失活,并在一定程度上使头孢呋辛失活。当向细菌培养物中添加β-内酰胺类抗生素时,克拉维酸可保护这两个菌种免受β-内酰胺酶的作用。

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