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首页> 外文期刊>World Journal of Microbiology and Biotechnology >In vitro antifungal activity of allicin alone and in combination with two medications against Trichophyton rubrum
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In vitro antifungal activity of allicin alone and in combination with two medications against Trichophyton rubrum

机译:大蒜素单独和与两种药物联合治疗对毛癣菌的体外抗真菌活性

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Dermatophytes are a group of fungi able to invade keratinized tissues of humans and animals, causing dermatomycosis. Azole antifungal drugs are commonly used in the treatment of dermatomycosis. However, this group of chemicals is known to cause side effects in patients and due to increased use of these medications, azoles are known to cause drug resistance. Having said this, the purpose of the present study was to investigate an alternative anti dermatophyte which is plant based. In this study, allicin, which is a pure bioactive compound isolated from garlic, was tested for its potential as a treatment of dermatomycosis. The study evaluated the in vitro efficacy of pure allicin used alone against ten isolates of Trichophyton rubrum and it was found that the MIC50 and MIC90 ranged from 0.78–25.0 μg/ml, whereas the MIC values for ketoconazole and fluconazole ranged from 0.25–8.0 and 1.0–32.0 μg/ml, respectively, at 28°C for both 7 and 10 days incubation. On the other hand, time–kill studies revealed that the antifungicidal effect of allicin became active within 12–24 h of management in vitro and that it was as good as that of ketoconazole. Finally, most of the tested drug combinations demonstrated synergistic or additive interactions for all isolates for both 7 and 10 days incubation at 28°C. In conclusion, when used alone, allicin showed very good potential as an antifungal compound against mycoses-causing dermatophytes, performing better than the synthetic drug fluconazole and almost as good as ketoconazole. Furthermore, allicin in combination with ketoconazole or with fluconazole frequently showed synergistic or additive interactions against dermatomycosis.
机译:皮肤癣菌是一组能够侵入人和动物的角化组织并引起皮肤癣菌的真菌。唑类抗真菌药通常用于治疗皮肤癣菌病。但是,已知这类化学物质会在患者中引起副作用,并且由于这些药物的使用增加,已知唑类会引起耐药性。话虽如此,本研究的目的是研究一种基于植物的替代抗皮肤癣菌。在这项研究中,大蒜素是一种纯净的生物活性化合物,它从大蒜中分离出来,具有潜在的治疗皮肤癣菌的能力。该研究评估了单独使用纯大蒜素对十株红毛癣菌的体外功效,结果发现MIC 50 和MIC 90 的范围为0.78–25.0μg/在28°C下孵育7天和10天,酮康唑和氟康唑的MIC值分别为0.25-8.0和1.0-32.0μg/ ml。另一方面,时间杀灭研究表明,大蒜素的抗真菌作用在体外处理后12至24小时内开始发挥作用,并且与酮康唑一样好。最后,大多数被测试的药物组合在28°C下孵育7天和10天对所有分离物均表现出协同或加性相互作用。总而言之,当单独使用大蒜素时,它具有很好的潜在潜力,可作为抗真菌化合物对抗由真菌引起的皮肤真菌,其性能优于合成药物氟康唑,几乎与酮康唑一样好。此外,大蒜素与酮康唑或氟康唑的组合经常表现出对抗皮癣的协同或加性相互作用。

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