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甲癣的新型和研究性治疗方法。

Novel and Investigational Treatments for Onychomycosis.

作者信息

Gregoriou Stamatios, Kyriazopoulou Maria, Tsiogka Aikaterini, Rigopoulos Dimitrios

机构信息

Department of Dermatology-Venereology, Faculty of Medicine, Andreas Sygros Hospital, National and Kapodistrian University of Athens, 16121 Athens, Greece.

出版信息

J Fungi (Basel). 2022 Oct 14;8(10):1079. doi: 10.3390/jof8101079.

Abstract

Onychomycosis is a common nail disease caused by fungi. The primary pathogens are dermatophytes; however, yeasts, non-dermatophyte moulds, and mixed fungal populations may also contribute to the development of a recalcitrant condition, usually accompanied by difficulties in everyday life and severe emotional stress. Treatment failure and relapse of the infection are the most frequent problems, though new issues have become the new challenges in the therapeutic approach to onychomycosis. Resistance to antifungals, an increasing number of comorbidities, and polydrug use among the ageing population are imperatives that impose a shift to safer drugs. Topical antifungals are considered less toxic and minimally interact with other drugs. The development of new topical drugs for onychomycosis is driven by the unmet need for effective agents with prolonged post-treatment disease-free time and a lack of systemic impact on the patients' health. Efinaconazole, Tavaborole, and Luliconazole have been added to physicians' weaponry during the last decade, though launched on the market of a limited number of countries. The pipeline is either developing new products (e.g., ME-1111 and NP213) with an appealing combination of pharmacokinetic, efficacy, and safety properties or reformulating old, well-known drugs (Terbinafine and Amphotericin B) by using new excipients as penetration enhancers.

摘要

甲癣是一种由真菌引起的常见指甲疾病。主要病原体是皮肤癣菌;然而,酵母菌、非皮肤癣菌霉菌以及混合真菌群体也可能导致难治性疾病的发生,通常会给日常生活带来困扰并造成严重的情绪压力。治疗失败和感染复发是最常见的问题,不过新问题已成为甲癣治疗方法中的新挑战。抗真菌药物耐药性、合并症数量增加以及老年人群中多种药物的使用,都促使人们转向使用更安全的药物。外用抗真菌药物被认为毒性较小,且与其他药物的相互作用极小。开发治疗甲癣的新型外用药物的动力在于,人们对具有延长治疗后无病时间且对患者健康无全身影响的有效药物存在未满足的需求。在过去十年中,艾氟康唑、他氟硼酸盐和卢立康唑已被纳入医生的治疗手段,尽管仅在少数国家上市。研发渠道要么是开发具有吸引人的药代动力学、疗效和安全性特性组合的新产品(如ME - 1111和NP213),要么是通过使用新辅料作为渗透促进剂来重新配制旧的知名药物(特比萘芬和两性霉素B)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7a9/9604567/272904c68c73/jof-08-01079-sch001.jpg

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