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首页> 外文期刊>Brazilian Journal of Microbiology >Antimicrobial effects of allicin and ketoconazole on trichophyton rubrum under in vitro condition
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Antimicrobial effects of allicin and ketoconazole on trichophyton rubrum under in vitro condition

机译:大蒜素和酮康唑在体外对红毛癣菌的抗菌作用

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Dermatophytosis is caused by a group of pathogenic fungi namely, dermatophytes, is among the most prevalent infectious diseases worldwide. Azole drugs are widely used in the treatment of dermatomycosis, but can cause various side effects and drug resistance to the patients. Hence, for solving this problem can be used from the plant extract as alternative for chemical drugs. Allicin is a pure bioactive compound isolated from garlic was tested for its potential as a treatment of dermatomycosis in this study. This study evaluated the in vitro efficacy of pure allicin against ten isolates of Trichophyton rubrum and the MIC50 and MIC90 ranged from 0.78-12.5 μg/ml for allicin. The results revealed that the order of efficacy based on the MICs values, all isolates showed almost comparable response to allicin and ketoconazole except for some isolates, at 28 oC for both 7 and 10 days incubation. Mann-Whitney test indicate that MICs at 7 days incubation was not observed a significant difference between the effects of allicin and ketoconazole (p 0.05), but MICs at 10 days incubation, a significant difference was observed (p < 0.05). On the other side, time kill studies revealed that allicin used its fungicidal activity within 12-24 h of management in vitro as well as ketoconazole. In conclusion, allicin showed very good potential as an antifungal compound against mycoses-causing dermatophytes, almost the same as the synthetic drug ketoconazole. Therefore, this antifungal agent appears to be effective, safe and suitable alternative for the treatment of dermatomycosis.
机译:皮肤癣菌病是由一组致病真菌,即皮肤癣菌引起的,是全世界最普遍的传染病之一。唑类药物被广泛用于治疗皮肤癣菌病,但可能对患者造成各种副作用和耐药性。因此,为了解决该问题,可以从植物提取物中使用其作为化学药物的替代品。大蒜素是一种从大蒜中分离出来的纯生物活性化合物,在这项研究中已测试了其大蒜素治疗皮肤癣菌的潜力。这项研究评估了纯大蒜素对十种红毛癣菌的体外功效,其大蒜素的MIC50和MIC90为0.78-12.5μg/ ml。结果显示,基于MIC值的功效顺序,所有分离株在28 oC下孵育7天和10天对除大蒜素和酮康唑的反应几乎与其他分离株相当。 Mann-Whitney测试表明,在培养7天时未观察到MIC的大蒜素和酮康唑的作用之间存在显着差异(p> 0.05),但是在培养10天时MIC观察到了显着差异(p <0.05)。另一方面,时间杀灭研究表明,大蒜素和酮康唑在体外处理后的12-24小时内都利用了其杀真菌活性。总之,大蒜素作为对抗真菌病的致皮肤真菌有很好的潜力,与合成药物酮康唑几乎一样。因此,这种抗真菌剂似乎是治疗皮肤癣菌病的有效,安全和合适的替代方法。

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