Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.

Onychomycosis, or fungal nail infection, is a common fungal infection largely caused by dermatophyte fungi, such as Trichophyton rubrum or Trichophyton mentagrophytes, which affects a significant number of people. Treatment is either through oral antifungal medicines, which are efficacious but have...

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Main Authors: Heather Davies-Strickleton, Julie Cook, Sally Hannam, Rhys Bennett, Alan Gibbs, David Edwards, Christine Ridden, John Ridden, David Cook
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0229414
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spelling doaj-b603c0cce8494bd7aa6313419ef7f1122021-03-03T21:30:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01152e022941410.1371/journal.pone.0229414Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.Heather Davies-StrickletonJulie CookSally HannamRhys BennettAlan GibbsDavid EdwardsChristine RiddenJohn RiddenDavid CookOnychomycosis, or fungal nail infection, is a common fungal infection largely caused by dermatophyte fungi, such as Trichophyton rubrum or Trichophyton mentagrophytes, which affects a significant number of people. Treatment is either through oral antifungal medicines, which are efficacious but have significant safety concerns, or with topical antifungal treatments that require long treatment regimens and have only limited efficacy. Thus, an efficacious topical therapy remains an unmet medical need. Among the barriers to topical delivery through the nail are the physico-chemical properties of the antifungal drugs. Here, we explore the ability of a range of antifungal compounds with different hydrophilicities to penetrate the nail. Human nail discs were clamped within static diffusion (Franz) cells and dosed with equimolar concentrations of antifungal drugs. Using LC-MS/MS we quantified the amount of drug that passed through the nail disc and that which remained associated with the nail. Our data identified increased drug flux through the nail for the more hydrophilic compounds (caffeine as a hydrophilic control and fluconazole, with LogP -0.07 and 0.5, respectively), while less hydrophilic efinaconazole, amorolfine and terbinafine (LogP 2.7, 5.6 and 5.9 respectively) had much lower flux through the nail. On the other hand, hydrophilicity alone did not account for the amount of drug associated with/bound to the nail itself. While there are other factors that are likely to combine to dictate nail penetration, this work supports earlier studies that implicate compound hydrophilicity as a critical factor for nail penetration.https://doi.org/10.1371/journal.pone.0229414
collection DOAJ
language English
format Article
sources DOAJ
author Heather Davies-Strickleton
Julie Cook
Sally Hannam
Rhys Bennett
Alan Gibbs
David Edwards
Christine Ridden
John Ridden
David Cook
spellingShingle Heather Davies-Strickleton
Julie Cook
Sally Hannam
Rhys Bennett
Alan Gibbs
David Edwards
Christine Ridden
John Ridden
David Cook
Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
PLoS ONE
author_facet Heather Davies-Strickleton
Julie Cook
Sally Hannam
Rhys Bennett
Alan Gibbs
David Edwards
Christine Ridden
John Ridden
David Cook
author_sort Heather Davies-Strickleton
title Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
title_short Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
title_full Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
title_fullStr Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
title_full_unstemmed Assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
title_sort assessment of the nail penetration of antifungal agents, with different physico-chemical properties.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Onychomycosis, or fungal nail infection, is a common fungal infection largely caused by dermatophyte fungi, such as Trichophyton rubrum or Trichophyton mentagrophytes, which affects a significant number of people. Treatment is either through oral antifungal medicines, which are efficacious but have significant safety concerns, or with topical antifungal treatments that require long treatment regimens and have only limited efficacy. Thus, an efficacious topical therapy remains an unmet medical need. Among the barriers to topical delivery through the nail are the physico-chemical properties of the antifungal drugs. Here, we explore the ability of a range of antifungal compounds with different hydrophilicities to penetrate the nail. Human nail discs were clamped within static diffusion (Franz) cells and dosed with equimolar concentrations of antifungal drugs. Using LC-MS/MS we quantified the amount of drug that passed through the nail disc and that which remained associated with the nail. Our data identified increased drug flux through the nail for the more hydrophilic compounds (caffeine as a hydrophilic control and fluconazole, with LogP -0.07 and 0.5, respectively), while less hydrophilic efinaconazole, amorolfine and terbinafine (LogP 2.7, 5.6 and 5.9 respectively) had much lower flux through the nail. On the other hand, hydrophilicity alone did not account for the amount of drug associated with/bound to the nail itself. While there are other factors that are likely to combine to dictate nail penetration, this work supports earlier studies that implicate compound hydrophilicity as a critical factor for nail penetration.
url https://doi.org/10.1371/journal.pone.0229414
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