A comparative study between two antifungal agents, luliconazole and efinaconazole, of their preventive effects in a trichophyton-infected guinea pig onychomycosis model

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Abstract

An efficacious period of two topical antifungal drugs was compared in a Trichophyton mentagrophytes-infected onychomycosis model in guinea pigs treated with antifungal drugs prior to infection. Luliconazole 5% (LLCZ) and efinaconazole 10% (EFCZ) test solutions were applied to the animals' nails once daily for 2 weeks followed by a nontreatment period of 2, 4, and 8 weeks. After each nontreatment period, the nails were artificially infected by the fungus. Drug efficacy was quantitatively evaluated by qPCR and histopathological examination of the nails collected following a 4-week post-infection period. The fungal infection was confirmed in the untreated group. Both LLCZ and EFCZ prevented fungal infection in the treated groups with the nontreatment period of 2 weeks. After the nontreatment period of 4 weeks, no infection was observed in the LLCZ-Treated group; however, infection into the nail surface and fungal invasion into the nail bed were observed in the EFCZ-Treated group. After the nontreatment period of 8 weeks, fungi were found in the nail surface and nail bed in some nails treated with EFCZ; however, no infection was observed in the nail bed of the LLCZ-Treated group. The results suggest that LLCZ possesses longer-lasting antifungal effect in nails of the guinea pigs than EFCZ, and that this animal model could be useful for translational research between preclinical and clinical studies to evaluate the pharmacological efficacy of antifungal drugs to treat onychomycosis. This experimentally shown longer-lasting preventive effects of LLCZ could also decrease the likelihoods of onychomycosis recurrence clinically.

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Nakamura, A., Hirakawa, S., Nagai, H., & Inagaki, K. (2021). A comparative study between two antifungal agents, luliconazole and efinaconazole, of their preventive effects in a trichophyton-infected guinea pig onychomycosis model. Medical Mycology, 59(3), 289–295. https://doi.org/10.1093/mmy/myaa111

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