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环吡酮胺和依氟康唑经皮渗透、抗真菌活性及诱导红色毛癣菌耐药的能力。

Ciclopirox and Efinaconazole Transungual Permeation, Antifungal Activity, and Proficiency To Induce Resistance in Trichophyton rubrum.

机构信息

Department of Pharmacy, University of Pisa, Pisa, Italy.

Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.

出版信息

Antimicrob Agents Chemother. 2019 Sep 23;63(10). doi: 10.1128/AAC.00442-19. Print 2019 Oct.

Abstract

Onychomycosis is a nail fungal infection, mostly caused by dermatophytes. The treatment efficacy is impaired by difficulties of reaching effective drug levels at the site of infection; frequent relapses occur after cessation of antifungal therapy. The aim of the study was to compare two commercial products containing ciclopirox or efinaconazole for antimycotic activity and antifungal drug resistance. A study of permeation and penetration through bovine hoof membranes, as a nail model, was performed to evaluate the antimycotic activity of permeates against clinical isolates of selected fungi, and the frequency of spontaneous -resistant strains was assessed by broth microdilution assays. The results suggest that ciclopirox creates a depot in the nail, leading to a gradual release of the drug over time with action on both the nail plate and bed. Conversely, efinaconazole, mildly interacting with nail keratin, mainly exerts its antifungal activity in the nail bed. However, in the case of , the antifungal activities of the drugs in the nail plate seem comparable. Finally, efinaconazole showed a potential for induction of resistance in , which may limit its efficacy over time. Ciclopirox did not show any potential to induce resistance in and appears endowed with a more complete activity than efinaconazole in the management of onychomycosis as the nail keratin is a substrate for the growth of fungal cells, and the availability of drug in large concentration just in the nail bed may not be sufficient to guarantee the complete eradication of pathogens.

摘要

甲真菌病是一种指甲真菌感染,主要由皮肤癣菌引起。由于难以在感染部位达到有效的药物水平,治疗效果受到影响;抗真菌治疗停止后经常复发。本研究的目的是比较两种含有环吡酮或依沙康唑的商业产品的抗真菌活性和抗真菌药物耐药性。通过牛蹄膜作为指甲模型进行渗透和穿透研究,评估渗透物对选定真菌临床分离株的抗真菌活性,并用肉汤微量稀释法评估自发耐药株的频率。结果表明,环吡酮在指甲中形成一个储库,导致药物随着时间的推移逐渐释放,对指甲板和床都有作用。相反,依沙康唑与指甲角蛋白轻度相互作用,主要在指甲床发挥抗真菌作用。然而,在这种情况下,药物在指甲板中的抗真菌活性似乎相当。最后,依沙康唑显示出在 中诱导耐药的潜力,这可能会限制其随着时间的推移的疗效。环吡酮在 中没有显示出任何诱导耐药的潜力,并且在治疗甲真菌病方面似乎比依沙康唑具有更完整的活性,因为指甲角蛋白是真菌细胞生长的底物,而且只有在指甲床中存在高浓度的药物可能不足以保证完全消除病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bbd/6761538/4cd54ef8db69/AAC.00442-19-f0001.jpg

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