首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Enhancement of the in vitro and in vivo activities of clarithromycin against Haemophilus influenzae by 14-hydroxy-clarithromycin its major metabolite in humans.
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Enhancement of the in vitro and in vivo activities of clarithromycin against Haemophilus influenzae by 14-hydroxy-clarithromycin its major metabolite in humans.

机译:14-羟基-克拉霉素它是人类的主要代谢产物可增强克拉霉素抗流感嗜血杆菌的体外和体内活性。

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摘要

MICs of clarithromycin and its major human metabolite, 14-hydroxy-clarithromycin, for Haemophilus influenzae in combination were reduced two- to fourfold compared with the MICs of each compound alone. Serum reduced the MICs of the parent compound and metabolite two- to fourfold compared with the MICs in medium without serum. In serum spiked with clinically relevant concentrations of clarithromycin and 14-hydroxy-clarithromycin at a fixed ratio of 4:1, 15 of 16 strains (94%) were inhibited and killed by combinations containing 1.2 and 0.3 micrograms/ml, respectively. In time kill experiments, the combination of parent compound and metabolite at one-fourth and one-half of their individual MICs, respectively, reduced bacterial counts by greater than 5 log CFU. The postantibiotic effect of clarithromycin combined with 14-hydroxy-clarithromycin was twice that of clarithromycin when tested alone. When orally administered to gerbils with H. influenzae otitis media, the 14-hydroxy metabolite was significantly more active than clarithromycin in reducing bacterial counts from the middle ear. The in vivo activity of the two compounds in combination was synergistic or additive, depending on the level of H. influenzae present at the time treatment was initiated. Significant reductions in bacterial counts and increases in cure rates were observed when clarithromycin at 50 or 100 mg/kg of body weight was combined with 14-hydroxy-clarithromycin at 12 mg/kg or higher. Results from in vitro and in vivo combinations suggest that routine susceptibility tests and animal efficacy studies with clarithromycin alone may underestimate its potential efficacy against H. influenzae.
机译:与单独使用每种化合物的MIC相比,组合使用的克拉霉素及其主要人类代谢物14-羟基-克拉霉素的MIC降低了2-4倍。与无血清培养基中的MIC相比,血清将母体化合物和代谢产物的MIC降低了2-4倍。在以固定比例4:1掺入临床相关浓度的克拉霉素和14-羟基克拉霉素的血清中,分别含有1.2和0.3微克/毫升的组合抑制和杀死16个菌株中的15个(94%)。在时间杀灭实验中,母体化合物和代谢物分别占其各自MIC的四分之一和二分之一时,细菌计数减少了超过5 log CFU。单独测试时,克拉霉素与14-羟基克拉霉素联合使用的后抗生素作用是克拉霉素的两倍。当对患有流感嗜血杆菌性中耳炎的沙鼠口服给药时,在减少中耳细菌计数方面,14-羟基代谢物的活性明显高于克拉霉素。取决于开始治疗时存在的流感嗜血杆菌的水平,两种化合物组合的体内活性是协同的或累加的。当以50或100 mg / kg体重的克拉霉素与12 mg / kg或更高的14-羟基克拉霉素联合使用时,观察到细菌数量的显着减少和治愈率的提高。体外和体内组合的结果表明,仅使用克拉霉素的常规药敏试验和动物功效研究可能低估了其对流感嗜血杆菌的潜在功效。

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