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A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells

The separation of rare cells from complex biofluids has attracted attention in biological research and clinical applications, especially for cancer detection and treatment. In particular, various technologies and methods have been developed for the isolation of circulating tumor cells (CTCs) in the...

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Autores principales: Manshadi, Mohammad K. D., Saadat, Mahsa, Mohammadi, Mehdi, Sanati Nezhad, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672846/
https://www.ncbi.nlm.nih.gov/pubmed/38004919
http://dx.doi.org/10.3390/mi14112062
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author Manshadi, Mohammad K. D.
Saadat, Mahsa
Mohammadi, Mehdi
Sanati Nezhad, Amir
author_facet Manshadi, Mohammad K. D.
Saadat, Mahsa
Mohammadi, Mehdi
Sanati Nezhad, Amir
author_sort Manshadi, Mohammad K. D.
collection PubMed
description The separation of rare cells from complex biofluids has attracted attention in biological research and clinical applications, especially for cancer detection and treatment. In particular, various technologies and methods have been developed for the isolation of circulating tumor cells (CTCs) in the blood. Among them, the induced-charge electrokinetic (ICEK) flow method has shown its high efficacy for cell manipulation where micro-vortices (MVs), generated as a result of induced charges on a polarizable surface, can effectively manipulate particles and cells in complex fluids. While the majority of MVs have been induced by AC electric fields, these vortices have also been observed under a DC electric field generated around a polarizable hurdle. In the present numerical work, the capability of MVs for the manipulation of CTCs and their entrapment in the DC electric field is investigated. First, the numerical results are verified against the available data in the literature. Then, various hurdle geometries are employed to find the most effective geometry for MV-based particle entrapment. The effects of electric field strength (EFS), wall zeta potential magnitude, and the particles’ diameter on the trapping efficacy are further investigated. The results demonstrated that the MVs generated around only the rectangular hurdle are capable of trapping particles as large as the size of CTCs. An EFS of about 75 V/cm was shown to be effective for the entrapment of above 90% of CTCs in the MVs. In addition, an EFS of 85 V/cm demonstrated a capability for isolating particles larger than 8 µm from a suspension of particles/cells 1–25 µm in diameter, useful for the enrichment of cancer cells and potentially for the real-time and non-invasive monitoring of drug effectiveness on circulating cancer cells in blood circulation.
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spelling pubmed-106728462023-11-05 A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells Manshadi, Mohammad K. D. Saadat, Mahsa Mohammadi, Mehdi Sanati Nezhad, Amir Micromachines (Basel) Article The separation of rare cells from complex biofluids has attracted attention in biological research and clinical applications, especially for cancer detection and treatment. In particular, various technologies and methods have been developed for the isolation of circulating tumor cells (CTCs) in the blood. Among them, the induced-charge electrokinetic (ICEK) flow method has shown its high efficacy for cell manipulation where micro-vortices (MVs), generated as a result of induced charges on a polarizable surface, can effectively manipulate particles and cells in complex fluids. While the majority of MVs have been induced by AC electric fields, these vortices have also been observed under a DC electric field generated around a polarizable hurdle. In the present numerical work, the capability of MVs for the manipulation of CTCs and their entrapment in the DC electric field is investigated. First, the numerical results are verified against the available data in the literature. Then, various hurdle geometries are employed to find the most effective geometry for MV-based particle entrapment. The effects of electric field strength (EFS), wall zeta potential magnitude, and the particles’ diameter on the trapping efficacy are further investigated. The results demonstrated that the MVs generated around only the rectangular hurdle are capable of trapping particles as large as the size of CTCs. An EFS of about 75 V/cm was shown to be effective for the entrapment of above 90% of CTCs in the MVs. In addition, an EFS of 85 V/cm demonstrated a capability for isolating particles larger than 8 µm from a suspension of particles/cells 1–25 µm in diameter, useful for the enrichment of cancer cells and potentially for the real-time and non-invasive monitoring of drug effectiveness on circulating cancer cells in blood circulation. MDPI 2023-11-05 /pmc/articles/PMC10672846/ /pubmed/38004919 http://dx.doi.org/10.3390/mi14112062 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Manshadi, Mohammad K. D.
Saadat, Mahsa
Mohammadi, Mehdi
Sanati Nezhad, Amir
A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells
title A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells
title_full A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells
title_fullStr A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells
title_full_unstemmed A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells
title_short A Novel Electrokinetic-Based Technique for the Isolation of Circulating Tumor Cells
title_sort novel electrokinetic-based technique for the isolation of circulating tumor cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672846/
https://www.ncbi.nlm.nih.gov/pubmed/38004919
http://dx.doi.org/10.3390/mi14112062
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