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Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy

PURPOSE: Through the characterisation of the human onchomycotic nail plate this study aimed to inform the design of new topical ungual formulations. METHODS: The mechanical properties of the human nail were characterised using a Lloyd tensile strength tester. The nail’s density was determined via py...

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Autores principales: Baraldi, A., Jones, S. A., Guesné, S., Traynor, M. J., McAuley, W. J., Brown, M. B., Murdan, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381097/
https://www.ncbi.nlm.nih.gov/pubmed/25416028
http://dx.doi.org/10.1007/s11095-014-1562-5
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author Baraldi, A.
Jones, S. A.
Guesné, S.
Traynor, M. J.
McAuley, W. J.
Brown, M. B.
Murdan, S.
author_facet Baraldi, A.
Jones, S. A.
Guesné, S.
Traynor, M. J.
McAuley, W. J.
Brown, M. B.
Murdan, S.
author_sort Baraldi, A.
collection PubMed
description PURPOSE: Through the characterisation of the human onchomycotic nail plate this study aimed to inform the design of new topical ungual formulations. METHODS: The mechanical properties of the human nail were characterised using a Lloyd tensile strength tester. The nail’s density was determined via pycnometry and the nail’s ultrastructure by electron microscopy. Raman spectroscopy analysed the keratin disulphide bonds within the nail and its permeability properties were assessed by quantifying water and rhodamine uptake. RESULTS: Chronic in vivo nail plate infection increased human nailplate thickness (healthy 0.49 ± 0.15 mm; diseased 1.20 ± 0.67 mm), but reduced its tensile strength (healthy 63.7 ± 13.4 MPa; diseased 41.7 ± 5.0 MPa) and density (healthy 1.34 ± 0.01 g/cm(3); diseased 1.29 ± 0.00 g/cm(3)). Onchomycosis caused cell-cell separation, without disrupting the nail disulfide bonds or desmosomes. The diseased and healthy nails showed equivalent water uptake profiles, but the rhodamine penetration was 4-fold higher in the diseased nails using a PBS vehicle and 3 -fold higher in an ethanol/PBS vehicle. CONCLUSIONS: Onchomycotic nails presented a thicker but more porous barrier, and its eroded intracellular matrix rendered the tissue more permeable to topically applied chemicals when an aqueous vehicle was used. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11095-014-1562-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-43810972015-04-07 Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy Baraldi, A. Jones, S. A. Guesné, S. Traynor, M. J. McAuley, W. J. Brown, M. B. Murdan, S. Pharm Res Research Paper PURPOSE: Through the characterisation of the human onchomycotic nail plate this study aimed to inform the design of new topical ungual formulations. METHODS: The mechanical properties of the human nail were characterised using a Lloyd tensile strength tester. The nail’s density was determined via pycnometry and the nail’s ultrastructure by electron microscopy. Raman spectroscopy analysed the keratin disulphide bonds within the nail and its permeability properties were assessed by quantifying water and rhodamine uptake. RESULTS: Chronic in vivo nail plate infection increased human nailplate thickness (healthy 0.49 ± 0.15 mm; diseased 1.20 ± 0.67 mm), but reduced its tensile strength (healthy 63.7 ± 13.4 MPa; diseased 41.7 ± 5.0 MPa) and density (healthy 1.34 ± 0.01 g/cm(3); diseased 1.29 ± 0.00 g/cm(3)). Onchomycosis caused cell-cell separation, without disrupting the nail disulfide bonds or desmosomes. The diseased and healthy nails showed equivalent water uptake profiles, but the rhodamine penetration was 4-fold higher in the diseased nails using a PBS vehicle and 3 -fold higher in an ethanol/PBS vehicle. CONCLUSIONS: Onchomycotic nails presented a thicker but more porous barrier, and its eroded intracellular matrix rendered the tissue more permeable to topically applied chemicals when an aqueous vehicle was used. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11095-014-1562-5) contains supplementary material, which is available to authorized users. Springer US 2014-11-22 2015 /pmc/articles/PMC4381097/ /pubmed/25416028 http://dx.doi.org/10.1007/s11095-014-1562-5 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research Paper
Baraldi, A.
Jones, S. A.
Guesné, S.
Traynor, M. J.
McAuley, W. J.
Brown, M. B.
Murdan, S.
Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy
title Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy
title_full Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy
title_fullStr Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy
title_full_unstemmed Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy
title_short Human Nail Plate Modifications Induced by Onychomycosis: Implications for Topical Therapy
title_sort human nail plate modifications induced by onychomycosis: implications for topical therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381097/
https://www.ncbi.nlm.nih.gov/pubmed/25416028
http://dx.doi.org/10.1007/s11095-014-1562-5
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