Fluid Dynamics Optimization of Microfluidic Diffusion Systems for Assessment of Transdermal Drug Delivery: An Experimental and Simulation Study

Author:

Kocsis Dorottya1ORCID,Dhinakaran Shanmugam2ORCID,Pandey Divyam2,Laki András József1,Laki Mária1,Sztankovics Dániel3ORCID,Lengyel Miléna4ORCID,Vrábel Judit1,Naszlady Márton Bese1ORCID,Sebestyén Anna3ORCID,Ponmozhi Jeyaraj5ORCID,Antal István4ORCID,Erdő Franciska1ORCID

Affiliation:

1. Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Práter u. 50a, 1083 Budapest, Hungary

2. The Centre for Fluid Dynamics, Department of Mechanical Engineering, Indian Institute of Technology Indore, Indore 453552, India

3. Department of Pathology and Experimental Cancer Research, Semmelweis University, Üllői út 26, 1085 Budapest, Hungary

4. Department of Pharmaceutics, Semmelweis University, Hőgyes Endre u. 7, 1092 Budapest, Hungary

5. Microfluidics Laboratory, Department of Mechanical Engineering, IPS Academy-Institute of Engineering Science, Indore 452012, India

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.

Funder

Ministry of Innovation and Technology, Hungary

National Research Development and Innovation Fund

ÚNKP-23-3 New National Excellence Program of the Ministry for Culture and Innovation from the National Research, Development, and Innovation Fund, Hungary

Science and Engineering Research Board

Publisher

MDPI AG

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