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Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings
Exosomes have gained recognition in cancer diagnostics and therapeutics. However, most exosome isolation methods are time-consuming, costly, and require bulky equipment, rendering them unsuitable for point-of-care (POC) settings. Microfluidics can be the key to solving these challenges. Here, we pre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574868/ https://www.ncbi.nlm.nih.gov/pubmed/37837121 http://dx.doi.org/10.3390/s23198292 |
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author | Ramnauth, Natasha Neubarth, Elise Makler-Disatham, Amy Sher, Mazhar Soini, Steven Merk, Vivian Asghar, Waseem |
author_facet | Ramnauth, Natasha Neubarth, Elise Makler-Disatham, Amy Sher, Mazhar Soini, Steven Merk, Vivian Asghar, Waseem |
author_sort | Ramnauth, Natasha |
collection | PubMed |
description | Exosomes have gained recognition in cancer diagnostics and therapeutics. However, most exosome isolation methods are time-consuming, costly, and require bulky equipment, rendering them unsuitable for point-of-care (POC) settings. Microfluidics can be the key to solving these challenges. Here, we present a double filtration microfluidic device that can rapidly isolate exosomes via size-exclusion principles in POC settings. The device can efficiently isolate exosomes from 50–100 µL of plasma within 50 min. The device was compared against an already established exosome isolation method, polyethylene glycol (PEG)-based precipitation. The findings showed that both methods yield comparable exosome sizes and purity; however, exosomes isolated from the device exhibited an earlier miRNA detection compared to exosomes obtained from the PEG-based isolation. A comparative analysis of exosomes collected from membrane filters with 15 nm and 30 nm pore sizes showed a similarity in exosome size and miRNA detection, with significantly increased sample purity. Finally, TEM images were taken to analyze how the developed devices and PEG-based isolation alter exosome morphology and to analyze exosome sizes. This developed microfluidic device is cost-efficient and time-efficient. Thus, it is ideal for use in low-resourced and POC settings to aid in cancer and disease diagnostics and therapeutics. |
format | Online Article Text |
id | pubmed-10574868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105748682023-10-14 Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings Ramnauth, Natasha Neubarth, Elise Makler-Disatham, Amy Sher, Mazhar Soini, Steven Merk, Vivian Asghar, Waseem Sensors (Basel) Article Exosomes have gained recognition in cancer diagnostics and therapeutics. However, most exosome isolation methods are time-consuming, costly, and require bulky equipment, rendering them unsuitable for point-of-care (POC) settings. Microfluidics can be the key to solving these challenges. Here, we present a double filtration microfluidic device that can rapidly isolate exosomes via size-exclusion principles in POC settings. The device can efficiently isolate exosomes from 50–100 µL of plasma within 50 min. The device was compared against an already established exosome isolation method, polyethylene glycol (PEG)-based precipitation. The findings showed that both methods yield comparable exosome sizes and purity; however, exosomes isolated from the device exhibited an earlier miRNA detection compared to exosomes obtained from the PEG-based isolation. A comparative analysis of exosomes collected from membrane filters with 15 nm and 30 nm pore sizes showed a similarity in exosome size and miRNA detection, with significantly increased sample purity. Finally, TEM images were taken to analyze how the developed devices and PEG-based isolation alter exosome morphology and to analyze exosome sizes. This developed microfluidic device is cost-efficient and time-efficient. Thus, it is ideal for use in low-resourced and POC settings to aid in cancer and disease diagnostics and therapeutics. MDPI 2023-10-07 /pmc/articles/PMC10574868/ /pubmed/37837121 http://dx.doi.org/10.3390/s23198292 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 Ramnauth, Natasha Neubarth, Elise Makler-Disatham, Amy Sher, Mazhar Soini, Steven Merk, Vivian Asghar, Waseem Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings |
title | Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings |
title_full | Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings |
title_fullStr | Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings |
title_full_unstemmed | Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings |
title_short | Development of a Microfluidic Device for Exosome Isolation in Point-of-Care Settings |
title_sort | development of a microfluidic device for exosome isolation in point-of-care settings |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574868/ https://www.ncbi.nlm.nih.gov/pubmed/37837121 http://dx.doi.org/10.3390/s23198292 |
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