Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/14166
Title: Fluid Dynamics Optimization of Microfluidic Diffusion Systems for Assessment of Transdermal Drug Delivery: An Experimental and Simulation Study
Authors: Shanmugam, Dhinakaran
Pandey, Divyam
Keywords: computational fluid dynamics;drug penetration;flow rate;microfluidic diffusion chambers;shear stress;skin on a chip;topical drugs;transdermal drug delivery;velocity
Issue Date: 2024
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
Citation: Kocsis, D., Dhinakaran, S., Pandey, D., Laki, A. J., Laki, M., Sztankovics, D., Lengyel, M., Vr�bel, J., Naszlady, M. B., Sebesty�n, A., Ponmozhi, J., Antal, I., & Erd?, F. (2024). Fluid Dynamics Optimization of Microfluidic Diffusion Systems for Assessment of Transdermal Drug Delivery: An Experimental and Simulation Study. Scientia Pharmaceutica. https://doi.org/10.3390/scipharm92020035
Abstract: Organ-on-a-chip technologies show exponential growth driven by the need to reduce the number of experimental animals and develop physiologically relevant human models for testing drugs. In vitro, microfluidic devices should be carefully designed and fabricated to provide reliable tools for modeling physiological or pathological conditions and assessing, for example, drug delivery through biological barriers. The aim of the current study was to optimize the utilization of three existing skin-on-a-chip microfluidic diffusion chambers with various designs. For this, different perfusion flow rates were compared using cellulose acetate membrane, polyester membrane, excised rat skin, and acellular alginate scaffold in the chips. These diffusion platforms were integrated into a single-channel microfluidic diffusion chamber, a multi-channel chamber, and the LiveBox2 system. The experimental results revealed that the 40 µL/min flow rate resulted in the highest diffusion of the hydrophilic model formulation (2% caffeine cream) in each system. The single-channel setup was used for further analysis by computational fluid dynamics simulation. The visualization of shear stress and fluid velocity within the microchannel and the presentation of caffeine progression with the perfusion fluid were consistent with the measured data. These findings contribute to the development and effective application of microfluidic systems for penetration testing. © 2024 by the authors.
URI: https://doi.org/10.3390/scipharm92020035
https://dspace.iiti.ac.in/handle/123456789/14166
ISSN: 0036-8709
Type of Material: Journal Article
Appears in Collections:Department of Mechanical Engineering

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