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High throughput imaging cytometer with acoustic focussing
We demonstrate an imaging flow cytometer that uses acoustic levitation to assemble cells and other particles into a sheet structure. This technique enables a high resolution, low noise CMOS camera to capture images of thousands of cells with each frame. While ultrasonic focussing has previously been...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of
Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5782801/ https://www.ncbi.nlm.nih.gov/pubmed/29456838 http://dx.doi.org/10.1039/c5ra19497k |
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author | Zmijan, Robert Jonnalagadda, Umesh S. Carugo, Dario Kochi, Yu Lemm, Elizabeth Packham, Graham Hill, Martyn Glynne-Jones, Peter |
author_facet | Zmijan, Robert Jonnalagadda, Umesh S. Carugo, Dario Kochi, Yu Lemm, Elizabeth Packham, Graham Hill, Martyn Glynne-Jones, Peter |
author_sort | Zmijan, Robert |
collection | PubMed |
description | We demonstrate an imaging flow cytometer that uses acoustic levitation to assemble cells and other particles into a sheet structure. This technique enables a high resolution, low noise CMOS camera to capture images of thousands of cells with each frame. While ultrasonic focussing has previously been demonstrated for 1D cytometry systems, extending the technology to a planar, much higher throughput format and integrating imaging is non-trivial, and represents a significant jump forward in capability, leading to diagnostic possibilities not achievable with current systems. A galvo mirror is used to track the images of the moving cells permitting exposure times of 10 ms at frame rates of 50 fps with motion blur of only a few pixels. At 80 fps, we demonstrate a throughput of 208 000 beads per second. We investigate the factors affecting motion blur and throughput, and demonstrate the system with fluorescent beads, leukaemia cells and a chondrocyte cell line. Cells require more time to reach the acoustic focus than beads, resulting in lower throughputs; however a longer device would remove this constraint. |
format | Online Article Text |
id | pubmed-5782801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of
Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-57828012018-02-15 High throughput imaging cytometer with acoustic focussing Zmijan, Robert Jonnalagadda, Umesh S. Carugo, Dario Kochi, Yu Lemm, Elizabeth Packham, Graham Hill, Martyn Glynne-Jones, Peter RSC Adv Chemistry We demonstrate an imaging flow cytometer that uses acoustic levitation to assemble cells and other particles into a sheet structure. This technique enables a high resolution, low noise CMOS camera to capture images of thousands of cells with each frame. While ultrasonic focussing has previously been demonstrated for 1D cytometry systems, extending the technology to a planar, much higher throughput format and integrating imaging is non-trivial, and represents a significant jump forward in capability, leading to diagnostic possibilities not achievable with current systems. A galvo mirror is used to track the images of the moving cells permitting exposure times of 10 ms at frame rates of 50 fps with motion blur of only a few pixels. At 80 fps, we demonstrate a throughput of 208 000 beads per second. We investigate the factors affecting motion blur and throughput, and demonstrate the system with fluorescent beads, leukaemia cells and a chondrocyte cell line. Cells require more time to reach the acoustic focus than beads, resulting in lower throughputs; however a longer device would remove this constraint. Royal Society of Chemistry 2015-10-31 2015-10-01 /pmc/articles/PMC5782801/ /pubmed/29456838 http://dx.doi.org/10.1039/c5ra19497k Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Zmijan, Robert Jonnalagadda, Umesh S. Carugo, Dario Kochi, Yu Lemm, Elizabeth Packham, Graham Hill, Martyn Glynne-Jones, Peter High throughput imaging cytometer with acoustic focussing |
title | High throughput imaging cytometer
with acoustic focussing
|
title_full | High throughput imaging cytometer
with acoustic focussing
|
title_fullStr | High throughput imaging cytometer
with acoustic focussing
|
title_full_unstemmed | High throughput imaging cytometer
with acoustic focussing
|
title_short | High throughput imaging cytometer
with acoustic focussing
|
title_sort | high throughput imaging cytometer
with acoustic focussing |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5782801/ https://www.ncbi.nlm.nih.gov/pubmed/29456838 http://dx.doi.org/10.1039/c5ra19497k |
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