Tabata Yuji, Takei-Masuda Naomi, Kubota Natsuki, Takahata Sho, Ohyama Makoto, Kaneda Kaori, Iida Maiko, Maebashi Kazunori
Meiji Seika Pharma Co., Ltd., Pharmaceutical Research Center, Yokohama, Japan
Meiji Seika Pharma Co., Ltd., Pharmaceutical Research Center, Yokohama, Japan.
Antimicrob Agents Chemother. 2015 Dec 7;60(2):1035-9. doi: 10.1128/AAC.01739-15. Print 2016 Feb.
Fungal nail infection (onychomycosis) is a prevalent disease in many areas of the world, with a high incidence approaching 23%. Available antifungals to treat the disease suffer from a number of disadvantages, necessitating the discovery of new efficacious and safe antifungals. Here, we evaluate the in vitro antifungal activity and nail penetration ability of ME1111, a novel antifungal agent, along with comparator drugs, including ciclopirox, amorolfine, terbinafine, and itraconazole. ME1111 showed potent antifungal activity against Trichophyton rubrum and Trichophyton mentagrophytes (the major etiologic agents of onychomycosis) strains isolated in Japan and reference fungal strains with an MIC range of 0.12 to 0.5 mg/liter and an MIC50 and MIC90 of 0.5 mg/liter for both. Importantly, none of the tested isolates showed an elevated ME1111 MIC. Moreover, the antifungal activity of ME1111 was minimally affected by 5% wool keratin powder in comparison to the other antifungals tested. The ME1111 solution was able to penetrate human nails and inhibit fungal growth in a dose-dependent manner according to the TurChub assay. In contrast, 8% ciclopirox and 5% amorolfine nail lacquers showed no activity under the same conditions. ME1111 demonstrated approximately 60-fold-greater selectivity in inhibition of Trichophyton spp. than of human cell lines. Our findings demonstrate that ME1111 possesses potent antidermatophyte activity, maintains this activity in the presence of keratin, and possesses excellent human nail permeability. These results suggest that ME1111 is a promising topical medication for the treatment of onychomycosis and therefore warrants further clinical evaluation.
甲真菌病在世界许多地区都是一种常见疾病,发病率很高,接近23%。现有的用于治疗该疾病的抗真菌药物存在许多缺点,因此需要发现新的有效且安全的抗真菌药物。在此,我们评估了新型抗真菌剂ME1111以及包括环吡酮、阿莫罗芬、特比萘芬和伊曲康唑在内的对照药物的体外抗真菌活性和指甲穿透能力。ME1111对在日本分离的红色毛癣菌和须癣毛癣菌(甲真菌病的主要病原体)菌株以及参考真菌菌株显示出强大的抗真菌活性,其MIC范围为0.12至0.5毫克/升,两者的MIC50和MIC90均为0.5毫克/升。重要的是,所有测试菌株的ME¬1111 MIC均未升高。此外,与其他测试的抗真菌药物相比,5%羊毛角蛋白粉对ME1111的抗真菌活性影响最小。根据TurChub试验,ME1111溶液能够穿透人指甲并以剂量依赖的方式抑制真菌生长。相比之下,8%环吡酮和5%阿莫罗芬指甲油在相同条件下没有活性。ME1111对毛癣菌属的抑制选择性比对人细胞系高约60倍。我们的研究结果表明,ME1111具有强大的抗皮肤癣菌活性,在角蛋白存在的情况下保持这种活性,并且具有优异的人指甲渗透性。这些结果表明,ME1111是一种有前景的用于治疗甲真菌病的局部用药,因此值得进一步进行临床评估。