Elabbasi Ali, Kadry Ahmed, Joseph Warren, Elewski Boni, Ghannoum Mahmoud
Case Western Reserve University, Cleveland, OH, USA.
Arizona College of Podiatric Medicine, Midwestern University, Glendale, AZ, USA.
Dermatol Ther (Heidelb). 2024 Sep;14(9):2495-2507. doi: 10.1007/s13555-024-01237-6. Epub 2024 Aug 12.
Topical antifungals for toenail onychomycosis must penetrate the nail to deliver an inhibitory concentration of free drug to the site of infection. In two ex vivo experiments, we tested the ability of topical antifungals to inhibit growth of Trichophyton rubrum and Trichophyton mentagrophytes, the most common causative fungi in toenail onychomycosis.
Seven topical antifungals were tested: three U.S. Food and Drug Administration-approved products indicated for onychomycosis (ciclopirox 8% lacquer; efinaconazole 10% solution; tavaborole 5% solution) and four over-the-counter (OTC) products for fungal infections (tolnaftate 1% and/or undecylenic acid 25% solutions). The ability to inhibit fungal growth was tested in the presence and absence of keratin. Products were applied either to human cadaverous nails or keratin-free cellulose disks prior to placement on an agar plate (radius: 85 mm) seeded with a clinical isolate of T. rubrum or T. mentagrophytes. After incubation, the zone of inhibition (ZI), defined as the radius of the area of no fungal growth, was recorded.
In the nail penetration assay, average ZIs for efinaconazole (T. rubrum: 82.1 mm; T. mentagrophytes: 63.8 mm) were significantly greater than those for tavaborole (63.5 mm; 39.1 mm), ciclopirox (7.4 mm; 3.6 mm) and all OTC products (range: 10.5-34.2 mm against both species; all P < 0.001). In the cellulose disk diffusion assay, efinaconazole and tavaborole demonstrated maximal antifungal activity against both species (ZIs = 85 mm); average ZIs against T. rubrum and T. mentagrophytes were smaller for ciclopirox (59.0 and 55.7 mm, respectively) and OTC products (range: 31.2-57.8 mm and 25.7-47.7 mm, respectively).
Among all antifungals tested, the ability to penetrate human toenails to inhibit growth of both T. rubrum and T. mentagrophytes was greatest for efinaconazole, followed by tavaborole. These results indicate superior transungual penetration of efinaconazole compared to the other antifungals, suggesting lower keratin binding in the nail.
用于治疗趾甲甲癣的外用抗真菌药必须穿透趾甲,将游离药物的抑制浓度传递至感染部位。在两项体外实验中,我们测试了外用抗真菌药抑制红色毛癣菌和须癣毛癣菌生长的能力,这两种真菌是趾甲甲癣最常见的致病真菌。
测试了七种外用抗真菌药:三种美国食品药品监督管理局批准用于甲癣的产品(8%环吡酮漆;10%艾氟康唑溶液;5%他氟硼酸盐溶液)和四种用于真菌感染的非处方(OTC)产品(1%托萘酯和/或25%十一烯酸溶液)。在有角蛋白和无角蛋白的情况下测试抑制真菌生长的能力。将产品应用于人体尸体趾甲或无角蛋白的纤维素圆盘上,然后放置在接种有红色毛癣菌或须癣毛癣菌临床分离株的琼脂平板(半径:85毫米)上。孵育后,记录抑制圈(ZI),即无真菌生长区域的半径。
在趾甲穿透试验中,艾氟康唑的平均抑制圈(红色毛癣菌:82.1毫米;须癣毛癣菌:63.8毫米)显著大于他氟硼酸盐(63.5毫米;39.1毫米)、环吡酮(7.4毫米;3.6毫米)和所有非处方产品(对两种真菌的范围:10.5 - 34.2毫米;所有P < 0.001)。在纤维素圆盘扩散试验中,艾氟康唑和他氟硼酸盐对两种真菌均表现出最大的抗真菌活性(抑制圈 = 85毫米);环吡酮(分别为59.0和55.7毫米)和非处方产品(范围分别为31.2 - 57.8毫米和25.7 - 47.7毫米)对红色毛癣菌和须癣毛癣菌的平均抑制圈较小。
在所有测试的抗真菌药中,艾氟康唑穿透人趾甲抑制红色毛癣菌和须癣毛癣菌生长的能力最强,其次是他氟硼酸盐。这些结果表明,与其他抗真菌药相比,艾氟康唑的经甲穿透性更佳,提示其在趾甲中的角蛋白结合较低。