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High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity

Circulating tumor cells (CTCs) are scarce cancer cells that rarely spread from primary or metastatic tumors inside the patient's bloodstream. Determining the genetic characteristics of these paranormal cells provides significant data to guide cancer staging and treatment. Cell focusing using mi...

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Autores principales: Omrani, Vahid, Targhi, Mohammad Zabetian, Rahbarizadeh, Fatemeh, Nosrati, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958115/
https://www.ncbi.nlm.nih.gov/pubmed/36828913
http://dx.doi.org/10.1038/s41598-023-30275-x
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author Omrani, Vahid
Targhi, Mohammad Zabetian
Rahbarizadeh, Fatemeh
Nosrati, Reza
author_facet Omrani, Vahid
Targhi, Mohammad Zabetian
Rahbarizadeh, Fatemeh
Nosrati, Reza
author_sort Omrani, Vahid
collection PubMed
description Circulating tumor cells (CTCs) are scarce cancer cells that rarely spread from primary or metastatic tumors inside the patient's bloodstream. Determining the genetic characteristics of these paranormal cells provides significant data to guide cancer staging and treatment. Cell focusing using microfluidic chips has been implemented as an effective method for enriching CTCs. The distinct equilibrium positions of particles with different diameters across the microchannel width in the simulation showed that it was possible to isolate and concentrate breast cancer cells (BCCs) from WBCs at a moderate Reynolds number. Therefore we demonstrate high throughput isolation of BCCs using a passive, size-based, label-free microfluidic method based on hydrodynamic forces by an unconventional (combination of long loops and U-turn) spiral microfluidic device for isolating both CTCs and WBCs with high efficiency and purity (more than 90%) at a flow rate about 1.7 mL/min, which has a high throughput compared to similar ones. At this golden flow rate, up to 92% of CTCs were separated from the cell suspension. Its rapid processing time, simplicity, and potential ability to collect CTCs from large volumes of patient blood allow the practical use of this method in many applications.
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spelling pubmed-99581152023-02-26 High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity Omrani, Vahid Targhi, Mohammad Zabetian Rahbarizadeh, Fatemeh Nosrati, Reza Sci Rep Article Circulating tumor cells (CTCs) are scarce cancer cells that rarely spread from primary or metastatic tumors inside the patient's bloodstream. Determining the genetic characteristics of these paranormal cells provides significant data to guide cancer staging and treatment. Cell focusing using microfluidic chips has been implemented as an effective method for enriching CTCs. The distinct equilibrium positions of particles with different diameters across the microchannel width in the simulation showed that it was possible to isolate and concentrate breast cancer cells (BCCs) from WBCs at a moderate Reynolds number. Therefore we demonstrate high throughput isolation of BCCs using a passive, size-based, label-free microfluidic method based on hydrodynamic forces by an unconventional (combination of long loops and U-turn) spiral microfluidic device for isolating both CTCs and WBCs with high efficiency and purity (more than 90%) at a flow rate about 1.7 mL/min, which has a high throughput compared to similar ones. At this golden flow rate, up to 92% of CTCs were separated from the cell suspension. Its rapid processing time, simplicity, and potential ability to collect CTCs from large volumes of patient blood allow the practical use of this method in many applications. Nature Publishing Group UK 2023-02-24 /pmc/articles/PMC9958115/ /pubmed/36828913 http://dx.doi.org/10.1038/s41598-023-30275-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Omrani, Vahid
Targhi, Mohammad Zabetian
Rahbarizadeh, Fatemeh
Nosrati, Reza
High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
title High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
title_full High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
title_fullStr High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
title_full_unstemmed High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
title_short High-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
title_sort high-throughput isolation of cancer cells in spiral microchannel by changing the direction, magnitude and location of the maximum velocity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958115/
https://www.ncbi.nlm.nih.gov/pubmed/36828913
http://dx.doi.org/10.1038/s41598-023-30275-x
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