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Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin
We report here on the application of laser-based single molecule total internal reflection fluorescence microscopy (TIRFM) to study the penetration of molecules through the skin. Penetration of topically applied drug molecules is often observed to be limited by the size of the respective drug. Howev...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424999/ https://www.ncbi.nlm.nih.gov/pubmed/25826528 http://dx.doi.org/10.3390/ijms16046960 |
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author | Volz, Pierre Boreham, Alexander Wolf, Alexander Kim, Tai-Yang Balke, Jens Frombach, Janna Hadam, Sabrina Afraz, Zahra Rancan, Fiorenza Blume-Peytavi, Ulrike Vogt, Annika Alexiev, Ulrike |
author_facet | Volz, Pierre Boreham, Alexander Wolf, Alexander Kim, Tai-Yang Balke, Jens Frombach, Janna Hadam, Sabrina Afraz, Zahra Rancan, Fiorenza Blume-Peytavi, Ulrike Vogt, Annika Alexiev, Ulrike |
author_sort | Volz, Pierre |
collection | PubMed |
description | We report here on the application of laser-based single molecule total internal reflection fluorescence microscopy (TIRFM) to study the penetration of molecules through the skin. Penetration of topically applied drug molecules is often observed to be limited by the size of the respective drug. However, the molecular mechanisms which govern the penetration of molecules through the outermost layer of the skin are still largely unknown. As a model compound we have chosen a larger amphiphilic molecule (fluorescent dye ATTO-Oxa12) with a molecular weight >700 Da that was applied to excised human skin. ATTO-Oxa12 penetrated through the stratum corneum (SC) into the viable epidermis as revealed by TIRFM of cryosections. Single particle tracking of ATTO-Oxa12 within SC sheets obtained by tape stripping allowed us to gain information on the localization as well as the lateral diffusion dynamics of these molecules. ATTO-Oxa12 appeared to be highly confined in the SC lipid region between (intercellular space) or close to the envelope of the corneocytes. Three main distinct confinement sizes of 52 ± 6, 118 ± 4, and 205 ± 5 nm were determined. We conclude that for this amphiphilic model compound several pathways through the skin exist. |
format | Online Article Text |
id | pubmed-4424999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44249992015-05-20 Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin Volz, Pierre Boreham, Alexander Wolf, Alexander Kim, Tai-Yang Balke, Jens Frombach, Janna Hadam, Sabrina Afraz, Zahra Rancan, Fiorenza Blume-Peytavi, Ulrike Vogt, Annika Alexiev, Ulrike Int J Mol Sci Article We report here on the application of laser-based single molecule total internal reflection fluorescence microscopy (TIRFM) to study the penetration of molecules through the skin. Penetration of topically applied drug molecules is often observed to be limited by the size of the respective drug. However, the molecular mechanisms which govern the penetration of molecules through the outermost layer of the skin are still largely unknown. As a model compound we have chosen a larger amphiphilic molecule (fluorescent dye ATTO-Oxa12) with a molecular weight >700 Da that was applied to excised human skin. ATTO-Oxa12 penetrated through the stratum corneum (SC) into the viable epidermis as revealed by TIRFM of cryosections. Single particle tracking of ATTO-Oxa12 within SC sheets obtained by tape stripping allowed us to gain information on the localization as well as the lateral diffusion dynamics of these molecules. ATTO-Oxa12 appeared to be highly confined in the SC lipid region between (intercellular space) or close to the envelope of the corneocytes. Three main distinct confinement sizes of 52 ± 6, 118 ± 4, and 205 ± 5 nm were determined. We conclude that for this amphiphilic model compound several pathways through the skin exist. MDPI 2015-03-27 /pmc/articles/PMC4424999/ /pubmed/25826528 http://dx.doi.org/10.3390/ijms16046960 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Volz, Pierre Boreham, Alexander Wolf, Alexander Kim, Tai-Yang Balke, Jens Frombach, Janna Hadam, Sabrina Afraz, Zahra Rancan, Fiorenza Blume-Peytavi, Ulrike Vogt, Annika Alexiev, Ulrike Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin |
title | Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin |
title_full | Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin |
title_fullStr | Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin |
title_full_unstemmed | Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin |
title_short | Application of Single Molecule Fluorescence Microscopy to Characterize the Penetration of a Large Amphiphilic Molecule in the Stratum Corneum of Human Skin |
title_sort | application of single molecule fluorescence microscopy to characterize the penetration of a large amphiphilic molecule in the stratum corneum of human skin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424999/ https://www.ncbi.nlm.nih.gov/pubmed/25826528 http://dx.doi.org/10.3390/ijms16046960 |
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