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MicroBubble activated acoustic cell sorting

Acoustophoresis, the ability to acoustically manipulate particles and cells inside a microfluidic channel, is a critical enabling technology for cell-sorting applications. However, one of the major impediments for routine use of acoustophoresis at clinical laboratory has been the reliance on the inh...

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Autores principales: Faridi, M. A., Ramachandraiah, H., Iranmanesh, I., Grishenkov, D., Wiklund, M., Russom, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378755/
https://www.ncbi.nlm.nih.gov/pubmed/28374278
http://dx.doi.org/10.1007/s10544-017-0157-4
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author Faridi, M. A.
Ramachandraiah, H.
Iranmanesh, I.
Grishenkov, D.
Wiklund, M.
Russom, A.
author_facet Faridi, M. A.
Ramachandraiah, H.
Iranmanesh, I.
Grishenkov, D.
Wiklund, M.
Russom, A.
author_sort Faridi, M. A.
collection PubMed
description Acoustophoresis, the ability to acoustically manipulate particles and cells inside a microfluidic channel, is a critical enabling technology for cell-sorting applications. However, one of the major impediments for routine use of acoustophoresis at clinical laboratory has been the reliance on the inherent physical properties of cells for separation. Here, we present a microfluidic-based microBubble-Activated Acoustic Cell Sorting (BAACS) method that rely on the specific binding of target cells to microbubbles conjugated with specific antibodies on their surface for continuous cell separation using ultrasonic standing wave. In acoustophoresis, cells being positive acoustic contrast particles migrate to pressure nodes. On the contrary, air-filled polymer-shelled microbubbles being strong negative acoustic contrast particles migrate to pressure antinodes and can be used to selectively migrate target cells. As a proof of principle, we demonstrate the separation of cancer cell line in a suspension with better than 75% efficiency. Moreover, 100% of the microbubble-cell conjugates migrated to the anti-node. Hence a better upstream affinity-capture has the potential to provide higher sorting efficiency. The BAACS technique expands the acoustic cell manipulation possibilities and offers cell-sorting solutions suited for applications at point of care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10544-017-0157-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-53787552017-04-17 MicroBubble activated acoustic cell sorting Faridi, M. A. Ramachandraiah, H. Iranmanesh, I. Grishenkov, D. Wiklund, M. Russom, A. Biomed Microdevices Article Acoustophoresis, the ability to acoustically manipulate particles and cells inside a microfluidic channel, is a critical enabling technology for cell-sorting applications. However, one of the major impediments for routine use of acoustophoresis at clinical laboratory has been the reliance on the inherent physical properties of cells for separation. Here, we present a microfluidic-based microBubble-Activated Acoustic Cell Sorting (BAACS) method that rely on the specific binding of target cells to microbubbles conjugated with specific antibodies on their surface for continuous cell separation using ultrasonic standing wave. In acoustophoresis, cells being positive acoustic contrast particles migrate to pressure nodes. On the contrary, air-filled polymer-shelled microbubbles being strong negative acoustic contrast particles migrate to pressure antinodes and can be used to selectively migrate target cells. As a proof of principle, we demonstrate the separation of cancer cell line in a suspension with better than 75% efficiency. Moreover, 100% of the microbubble-cell conjugates migrated to the anti-node. Hence a better upstream affinity-capture has the potential to provide higher sorting efficiency. The BAACS technique expands the acoustic cell manipulation possibilities and offers cell-sorting solutions suited for applications at point of care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10544-017-0157-4) contains supplementary material, which is available to authorized users. Springer US 2017-04-03 2017 /pmc/articles/PMC5378755/ /pubmed/28374278 http://dx.doi.org/10.1007/s10544-017-0157-4 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Faridi, M. A.
Ramachandraiah, H.
Iranmanesh, I.
Grishenkov, D.
Wiklund, M.
Russom, A.
MicroBubble activated acoustic cell sorting
title MicroBubble activated acoustic cell sorting
title_full MicroBubble activated acoustic cell sorting
title_fullStr MicroBubble activated acoustic cell sorting
title_full_unstemmed MicroBubble activated acoustic cell sorting
title_short MicroBubble activated acoustic cell sorting
title_sort microbubble activated acoustic cell sorting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378755/
https://www.ncbi.nlm.nih.gov/pubmed/28374278
http://dx.doi.org/10.1007/s10544-017-0157-4
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