A Transdermal Measurement Platform Based on Microfluidics

The Franz diffusion cell is one of the most widely used devices to evaluate transdermal drug delivery. However, this static and nonflowing system has some limitations, such as a relatively large solution volume and skin area and the development of gas bubbles during sampling. To overcome these disad...

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Main Authors: Wen-Ying Huang, Jung-Ping Huang, Chia-Ching Lin, Yung-Sheng Lin
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2017/9343824
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spelling doaj-df295d2dddc443e3a8295f24ca3ec6e02020-11-24T21:42:13ZengHindawi LimitedJournal of Chemistry2090-90632090-90712017-01-01201710.1155/2017/93438249343824A Transdermal Measurement Platform Based on MicrofluidicsWen-Ying Huang0Jung-Ping Huang1Chia-Ching Lin2Yung-Sheng Lin3Department of Applied Cosmetology and Master Program of Cosmetic Science, Hungkuang University, Taichung 43302, TaiwanDepartment of Applied Cosmetology and Master Program of Cosmetic Science, Hungkuang University, Taichung 43302, TaiwanDepartment of Applied Cosmetology and Master Program of Cosmetic Science, Hungkuang University, Taichung 43302, TaiwanDepartment of Chemical Engineering, National United University, Miaoli 36063, TaiwanThe Franz diffusion cell is one of the most widely used devices to evaluate transdermal drug delivery. However, this static and nonflowing system has some limitations, such as a relatively large solution volume and skin area and the development of gas bubbles during sampling. To overcome these disadvantages, this study provides a proof of concept for miniaturizing models of transdermal delivery by using a microfluidic chip combined with a diffusion cell. The proposed diffusion microchip system requires only 80 μL of sample solution and provides flow circulation. Two model compounds, Coomassie Brilliant Blue G-250 and potassium ferricyanide, were successfully tested for transdermal delivery experiments. The diffusion rate is high for a high sample concentration or a large membrane pore size. The developed diffusion microchip system, which is feasible, can be applied for transdermal measurement in the future.http://dx.doi.org/10.1155/2017/9343824
collection DOAJ
language English
format Article
sources DOAJ
author Wen-Ying Huang
Jung-Ping Huang
Chia-Ching Lin
Yung-Sheng Lin
spellingShingle Wen-Ying Huang
Jung-Ping Huang
Chia-Ching Lin
Yung-Sheng Lin
A Transdermal Measurement Platform Based on Microfluidics
Journal of Chemistry
author_facet Wen-Ying Huang
Jung-Ping Huang
Chia-Ching Lin
Yung-Sheng Lin
author_sort Wen-Ying Huang
title A Transdermal Measurement Platform Based on Microfluidics
title_short A Transdermal Measurement Platform Based on Microfluidics
title_full A Transdermal Measurement Platform Based on Microfluidics
title_fullStr A Transdermal Measurement Platform Based on Microfluidics
title_full_unstemmed A Transdermal Measurement Platform Based on Microfluidics
title_sort transdermal measurement platform based on microfluidics
publisher Hindawi Limited
series Journal of Chemistry
issn 2090-9063
2090-9071
publishDate 2017-01-01
description The Franz diffusion cell is one of the most widely used devices to evaluate transdermal drug delivery. However, this static and nonflowing system has some limitations, such as a relatively large solution volume and skin area and the development of gas bubbles during sampling. To overcome these disadvantages, this study provides a proof of concept for miniaturizing models of transdermal delivery by using a microfluidic chip combined with a diffusion cell. The proposed diffusion microchip system requires only 80 μL of sample solution and provides flow circulation. Two model compounds, Coomassie Brilliant Blue G-250 and potassium ferricyanide, were successfully tested for transdermal delivery experiments. The diffusion rate is high for a high sample concentration or a large membrane pore size. The developed diffusion microchip system, which is feasible, can be applied for transdermal measurement in the future.
url http://dx.doi.org/10.1155/2017/9343824
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