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CP-45899 in combination with penicillin or ampicillin against penicillin-resistant Staphylococcus Haemophilus influenzae and Bacteroides.

机译:CP-45899与青霉素或氨苄青霉素联用可抵抗耐青霉素的葡萄球菌流感嗜血杆菌和拟杆菌。

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摘要

CP-45,899 is a new, semisynthetic beta-lactamase inhibitor. When tested alone, CP-45,899 displayed only weak antibacterial activity, with the notable exception of its potent action against penicillin-susceptible and -resistant Neisseria gonorrhoeae. A combination of 3.12 microgram of CP-45,899 per ml with 3.12 microgram of ampicillin per ml, tested in broth cultures, inhibited ca. 90% of resistant Staphylococcus and Haemophilus influenzae strains; similar data were obtained in a variety of media. The same combination of CP-45,899 with ampicillin or penicillin G inhibited 90% of Bacteroides fragilis as interpreted from agar dilution minimal inhibitory concentrations. Inhibitory concentrations of CP-45,899-ampicillin were bactericidal against H. influenzae strains and were as bactericidal as nafcillin or cephalothin against S. aureus. Ampicillin-resistant S. aureus, H. influenzae, and B. fragilis strains did not develop resistance to CP-45,899-ampicillin when transferred as many as six passages in the presence of a sublethal concentration of the combination.
机译:CP-45,899是一种新型的半合成β-内酰胺酶抑制剂。单独测试时,CP-45,899仅表现出较弱的抗菌活性,但其对青霉素敏感性和耐药性淋病奈瑟氏球菌的有效作用明显例外。在肉汤培养中测试,每毫升3.12微克CP-45,899与每毫升3.12微克氨苄青霉素的结合可抑制约90%的耐药葡萄球菌和流感嗜血杆菌菌株;在各种媒体上也获得了类似的数据。 CP-45,899与氨苄青霉素或青霉素G的相同组合可抑制90%的脆弱拟杆菌,从琼脂稀释的最低抑菌浓度可以看出。 CP-45,899-氨苄青霉素的抑制浓度对流感嗜血杆菌菌株具有杀菌作用,与纳夫西林或头孢菌素对金黄色葡萄球菌一样具有杀菌作用。当在亚致死浓度的组合中转移多达六代时,耐氨苄青霉素的金黄色葡萄球菌,流感嗜血杆菌和脆弱的芽孢杆菌菌株未产生对CP-45,899-氨苄青霉素的抗性。

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