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Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation
BACKGROUND: Transdermal delivery is of great importance for the effective delivery of bioactive or therapeutic agents into a body. The microporation device based on radiofrequency can be used to enhance delivery efficiency by removing the epidermis layer. METHODS: The micropores were developed on pi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724873/ https://www.ncbi.nlm.nih.gov/pubmed/33298195 http://dx.doi.org/10.1186/s40824-020-00201-7 |
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author | Ahn, Guk Young Eo, Hae-Seok Kim, Dongwon Choi, Sung-Wook |
author_facet | Ahn, Guk Young Eo, Hae-Seok Kim, Dongwon Choi, Sung-Wook |
author_sort | Ahn, Guk Young |
collection | PubMed |
description | BACKGROUND: Transdermal delivery is of great importance for the effective delivery of bioactive or therapeutic agents into a body. The microporation device based on radiofrequency can be used to enhance delivery efficiency by removing the epidermis layer. METHODS: The micropores were developed on pig skin and human cadaver skin with dermal and epidermal layers by the microporation device. The regeneration of micropores in the human cadaver skin caused by microporation was confirmed using an optical microscope and haematoxylin/eosin (H&E) staining. The permeability of fluorescein isothiocyanate-dextrans (FITC-dextrans) with different molecular weights through the pig and human cadaver skins were measured using Franz diffusion cell. RESULTS: The optical image and histological analysis confirmed that the micropores on the skin were recovered over time. The enhanced permeability through micropores was confirmed by Franz diffusion cell. The lower molecular weight of FITC-dextran permeated more on both human and pig skin. In addition, the permeation rate was higher in pig skin than in human skin. CONCLUSIONS: We believe that the microporation device can be used as a potential technique for effective transdermal drug delivery. |
format | Online Article Text |
id | pubmed-7724873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77248732020-12-09 Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation Ahn, Guk Young Eo, Hae-Seok Kim, Dongwon Choi, Sung-Wook Biomater Res Research Article BACKGROUND: Transdermal delivery is of great importance for the effective delivery of bioactive or therapeutic agents into a body. The microporation device based on radiofrequency can be used to enhance delivery efficiency by removing the epidermis layer. METHODS: The micropores were developed on pig skin and human cadaver skin with dermal and epidermal layers by the microporation device. The regeneration of micropores in the human cadaver skin caused by microporation was confirmed using an optical microscope and haematoxylin/eosin (H&E) staining. The permeability of fluorescein isothiocyanate-dextrans (FITC-dextrans) with different molecular weights through the pig and human cadaver skins were measured using Franz diffusion cell. RESULTS: The optical image and histological analysis confirmed that the micropores on the skin were recovered over time. The enhanced permeability through micropores was confirmed by Franz diffusion cell. The lower molecular weight of FITC-dextran permeated more on both human and pig skin. In addition, the permeation rate was higher in pig skin than in human skin. CONCLUSIONS: We believe that the microporation device can be used as a potential technique for effective transdermal drug delivery. BioMed Central 2020-12-09 /pmc/articles/PMC7724873/ /pubmed/33298195 http://dx.doi.org/10.1186/s40824-020-00201-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Ahn, Guk Young Eo, Hae-Seok Kim, Dongwon Choi, Sung-Wook Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation |
title | Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation |
title_full | Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation |
title_fullStr | Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation |
title_full_unstemmed | Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation |
title_short | Transdermal delivery of FITC-Dextrans with different molecular weights using radiofrequency microporation |
title_sort | transdermal delivery of fitc-dextrans with different molecular weights using radiofrequency microporation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724873/ https://www.ncbi.nlm.nih.gov/pubmed/33298195 http://dx.doi.org/10.1186/s40824-020-00201-7 |
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