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Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells

Analysis at the single cell level has becoming an increasingly important procedure to diagnose cancer tissue biopsies. These tissue samples are often heterogeneous and consist of 1000–15,000 cells. We study the use of centrifugal microfluidics to isolate single cells into micro chambers. We describe...

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Detalles Bibliográficos
Autores principales: Snider, Adam, Pirozzi, Ileana, Tripathi, Anubhav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074746/
https://www.ncbi.nlm.nih.gov/pubmed/32013161
http://dx.doi.org/10.3390/mi11020149
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author Snider, Adam
Pirozzi, Ileana
Tripathi, Anubhav
author_facet Snider, Adam
Pirozzi, Ileana
Tripathi, Anubhav
author_sort Snider, Adam
collection PubMed
description Analysis at the single cell level has becoming an increasingly important procedure to diagnose cancer tissue biopsies. These tissue samples are often heterogeneous and consist of 1000–15,000 cells. We study the use of centrifugal microfluidics to isolate single cells into micro chambers. We describe the optimization of our microfluidics flow device, characterize its performance using both polystyrene beads as a cell analogue and MCF-7 breast cancer cells, and discuss potential applications for the device. Our results show rapid isolation of ~2000 single cell aliquots in ~20 min. We were able to occupy 65% of available chambers with singly occupied cancer cells, and observed capture efficiencies as high as 80% using input samples ranging from 2000 to 15,000 cells in 20 min. We believe our device is a valuable research tool that addresses the unmet need for massively parallel single cell level analysis of cell populations.
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spelling pubmed-70747462020-03-20 Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells Snider, Adam Pirozzi, Ileana Tripathi, Anubhav Micromachines (Basel) Article Analysis at the single cell level has becoming an increasingly important procedure to diagnose cancer tissue biopsies. These tissue samples are often heterogeneous and consist of 1000–15,000 cells. We study the use of centrifugal microfluidics to isolate single cells into micro chambers. We describe the optimization of our microfluidics flow device, characterize its performance using both polystyrene beads as a cell analogue and MCF-7 breast cancer cells, and discuss potential applications for the device. Our results show rapid isolation of ~2000 single cell aliquots in ~20 min. We were able to occupy 65% of available chambers with singly occupied cancer cells, and observed capture efficiencies as high as 80% using input samples ranging from 2000 to 15,000 cells in 20 min. We believe our device is a valuable research tool that addresses the unmet need for massively parallel single cell level analysis of cell populations. MDPI 2020-01-29 /pmc/articles/PMC7074746/ /pubmed/32013161 http://dx.doi.org/10.3390/mi11020149 Text en © 2020 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Snider, Adam
Pirozzi, Ileana
Tripathi, Anubhav
Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells
title Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells
title_full Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells
title_fullStr Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells
title_full_unstemmed Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells
title_short Centrifugal Microfluidics Traps for Parallel Isolation and Imaging of Single Cells
title_sort centrifugal microfluidics traps for parallel isolation and imaging of single cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074746/
https://www.ncbi.nlm.nih.gov/pubmed/32013161
http://dx.doi.org/10.3390/mi11020149
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