Numerical simulation of a multi-inlet microfluidic device for biosensing purposes in osteoporosis management.

Biosensor Microchips Microfluidic Simulation

Journal

Journal of diabetes and metabolic disorders
ISSN: 2251-6581
Titre abrégé: J Diabetes Metab Disord
Pays: Switzerland
ID NLM: 101590741

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 07 08 2018
accepted: 12 06 2019
entrez: 1 1 2020
pubmed: 1 1 2020
medline: 1 1 2020
Statut: epublish

Résumé

In this paper, the effect of the position of the inlet and outlet microchannels on the flow profile and the geometry of the recognition chamber for sample pre-treatment in an electrochemical biosensor to be used in osteoporosis management were investigated. All numerical computation presented in this work were performed using COMSOL Multiphysics and Fluent. Simulation was performed for a three-dimensional, incompressible Navier-Stokes flow and so explicit biphasic volume of fluid (VOF) equations were used. In the designed microfluidic system, a pressure-driven laminar flow with no-slip boundary condition was responsible for fluid actuation through microchannels in a reproducible approach. Based on the simulation results, the number of outlets was increased and the angel through which the inlets and outlets were attached to the microchamber was changed so that the dead volume would be eliminated and the fluid flow trajectory, the velocity field and pressure were evenly distributed across the chamber. The Re number in the inlets was equal to 4.41, suggesting a laminar flow at this site. The simulation results along with the fact that the design change was tested using laser ablated tape and a color dye at different steps provided the researchers with the opportunity to study the changes in a fast and accurate but cheap method. The absence of backflow helps with the cross-talk concern in the channels and the lack of bubbles and complete coverage of the chamber helps with a better surface modification and thus better sensing performance.

Identifiants

pubmed: 31890659
doi: 10.1007/s40200-019-00418-x
pii: 418
pmc: PMC6915250
doi:

Types de publication

Journal Article

Langues

eng

Pagination

341-348

Informations de copyright

© Springer Nature Switzerland AG 2019.

Déclaration de conflit d'intérêts

Conflict of interestThe authors declared that they have no conflict of interest.

Références

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pubmed: 24622198

Auteurs

Patricia Khashayar (P)

1Center for Microsystems Technology, Imec and Ghent University, Ghent, Zwijnaarde Belgium.
2Osteoporosis Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
3Nanobiotechnalogy Department, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.

Amir Okhovat (A)

4TeyfPardaz Pishroo, University of Yazd, Tehran, Iran.

Hossein Adibi (H)

5Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Jindrich Windels (J)

1Center for Microsystems Technology, Imec and Ghent University, Ghent, Zwijnaarde Belgium.

Ghassem Amoabediny (G)

3Nanobiotechnalogy Department, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.
6Department of Biotechnology, Faculty of Chemical Engineering, School of Engineering, University of Tehran, Tehran, Iran.

Bagher Larijani (B)

5Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Jan Vanfleteren (J)

1Center for Microsystems Technology, Imec and Ghent University, Ghent, Zwijnaarde Belgium.

Classifications MeSH