Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32710
Full metadata record
DC FieldValueLanguage
dc.contributor.authorHadjiaghaie Vafaie, R-
dc.contributor.authorPoorreza, E-
dc.contributor.authorSheykhivand, S-
dc.contributor.authorDanishvar, S-
dc.date.accessioned2026-01-23T17:42:52Z-
dc.date.available2026-01-23T17:42:52Z-
dc.date.issued2025-11-07-
dc.identifierORCiD: Reza Hadjiaghaie Vafaie https://orcid.org/0000-0003-4266-9880-
dc.identifierORCiD: Sebelan Danishvar https://orcid.org/0000-0002-8258-0437-
dc.identifierArticle number: 753-
dc.identifier.citationHadjiaghaie Vafaie, R. et al. (2025) 'A Bionic Sensing Platform for Cell Separation: Simulation of a Dielectrophoretic Microfluidic Device That Leverages Dielectric Fingerprints', Biomimetics, 10 (11), 753, pp. 1 - 24. doi: 10.3390/biomimetics10110753.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/32710-
dc.descriptionData Availability Statement: The raw data supporting the conclusions of this article will be made available by the authors on request.en_US
dc.description.abstractCancers are diseases described by the irregular spread of cells that have developed invasive features, enabling them to invade adjacent tissues. The specific diagnosis and effective management of oncological treatments depend on the timely detection of circulating tumor cells (CTCs) in a patient’s bloodstream. One of the most promising approaches to CTC separation from blood fractions involves the dielectrophoresis (DEP) technique. This research presents a new DEP-based bionic system designed for MDA-MB-231 breast cancer cell isolation from white blood cell (WBC) subtypes with a viable approach to cell viability. This work leverages the principle that every cell type possesses a unique dielectric fingerprint. This dielectrophoresis microfluidic device is designed to act as a scanner, reading these fingerprints to achieve a continuous, label-free separation of cancer cells from blood components with a high efficiency. In the proposed system that consists of three different stages, the first stage allows for separating B-lymphocytes and Monocytes from Granulocytes and MDA-MB-231 cells. The separation of B-lymphocytes from Monocytes occurs in the second step, while the last step concerns the separation of Granulocytes and MDA-MB-231 cells. In the analysis, x-y graphs of the electric potentials, velocity fields, pressure distributions, and cellular DEP forces applied to the cells, as well as the resulting particle paths, are provided. The model predicts that the system operates with a separation efficiency of nearly 92%. This work focuses on an investigation of the impact of electrode potentials, the velocity of cells, the number of electrodes, the width of the channel, and the output angles on enhancing the separation efficiency of particles.en_US
dc.description.sponsorshipThis research received no external funding.en_US
dc.format.extent1 - 24-
dc.format.mediumElectronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.rightsCreative Commons Attribution 4.0 International-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectbionicen_US
dc.subjectdielectrophoresis separationen_US
dc.subjectbiomedicalen_US
dc.subjectcanceren_US
dc.subjectcirculating tumor cellsen_US
dc.subjectmicrofluidicsen_US
dc.titleA Bionic Sensing Platform for Cell Separation: Simulation of a Dielectrophoretic Microfluidic Device That Leverages Dielectric Fingerprintsen_US
dc.typeArticleen_US
dc.date.dateAccepted2025-11-05-
dc.identifier.doihttps://doi.org/10.3390/biomimetics10110753-
dc.relation.isPartOfBiomimetics-
pubs.issue11-
pubs.publication-statusPublished-
pubs.volume10-
dc.identifier.eissn2313-7673-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/legalcode.en-
dcterms.dateAccepted2025-11-05-
dc.rights.holderThe authors-
dc.contributor.orcidHadjiaghaie Vafaie, Reza [0000-0003-4266-9880]-
dc.contributor.orcidDanishvar, Sebelan [0000-0002-8258-0437]-
Appears in Collections:Dept of Mechanical and Aerospace Engineering Research Papers

Files in This Item:
File Description SizeFormat 
FullText.pdfCopyright © 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).6.19 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons