Rapid cell separation with minimal manipulation for autologous cell therapies

The ability to isolate specific, viable cell populations from mixed ensembles with minimal manipulation and within intra-operative time would provide significant advantages for autologous, cell-based therapies in regenerative medicine. Current cell-enrichment technologies are either slow, lack speci...

Full description

Saved in:
Bibliographic Details
Main Authors: Smith, Alban J., O’Rorke, Richard D., Kale, Akshay, Rimsa, Roberts, Tomlinson, Matthew J., Kirkham, Jennifer, Davies, A. Giles, Wälti, Christoph, Wood, Christopher D.
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2018
Subjects:
Online Access:https://hdl.handle.net/10356/87589
http://hdl.handle.net/10220/45460
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-87589
record_format dspace
spelling sg-ntu-dr.10356-875892023-07-14T15:51:57Z Rapid cell separation with minimal manipulation for autologous cell therapies Smith, Alban J. O’Rorke, Richard D. Kale, Akshay Rimsa, Roberts Tomlinson, Matthew J. Kirkham, Jennifer Davies, A. Giles Wälti, Christoph Wood, Christopher D. School of Materials Science & Engineering Minimal Manipulation Autologous Cell Therapies The ability to isolate specific, viable cell populations from mixed ensembles with minimal manipulation and within intra-operative time would provide significant advantages for autologous, cell-based therapies in regenerative medicine. Current cell-enrichment technologies are either slow, lack specificity and/or require labelling. Thus a rapid, label-free separation technology that does not affect cell functionality, viability or phenotype is highly desirable. Here, we demonstrate separation of viable from non-viable human stromal cells using remote dielectrophoresis, in which an electric field is coupled into a microfluidic channel using shear-horizontal surface acoustic waves, producing an array of virtual electrodes within the channel. This allows high-throughput dielectrophoretic cell separation in high conductivity, physiological-like fluids, overcoming the limitations of conventional dielectrophoresis. We demonstrate viable/non-viable separation efficacy of >98% in pre-purified mesenchymal stromal cells, extracted from human dental pulp, with no adverse effects on cell viability, or on their subsequent osteogenic capabilities. Published version 2018-08-06T04:20:26Z 2019-12-06T16:45:08Z 2018-08-06T04:20:26Z 2019-12-06T16:45:08Z 2017 Journal Article Smith, A. J., O’Rorke, R. D., Kale, A., Rimsa, R., Tomlinson, M. J., Kirkham, J., et al. (2017). Rapid cell separation with minimal manipulation for autologous cell therapies. Scientific Reports, 7, 41872-. 2045-2322 https://hdl.handle.net/10356/87589 http://hdl.handle.net/10220/45460 10.1038/srep41872 en Scientific Reports © 2017 The Author(s). This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ 15 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Minimal Manipulation
Autologous Cell Therapies
spellingShingle Minimal Manipulation
Autologous Cell Therapies
Smith, Alban J.
O’Rorke, Richard D.
Kale, Akshay
Rimsa, Roberts
Tomlinson, Matthew J.
Kirkham, Jennifer
Davies, A. Giles
Wälti, Christoph
Wood, Christopher D.
Rapid cell separation with minimal manipulation for autologous cell therapies
description The ability to isolate specific, viable cell populations from mixed ensembles with minimal manipulation and within intra-operative time would provide significant advantages for autologous, cell-based therapies in regenerative medicine. Current cell-enrichment technologies are either slow, lack specificity and/or require labelling. Thus a rapid, label-free separation technology that does not affect cell functionality, viability or phenotype is highly desirable. Here, we demonstrate separation of viable from non-viable human stromal cells using remote dielectrophoresis, in which an electric field is coupled into a microfluidic channel using shear-horizontal surface acoustic waves, producing an array of virtual electrodes within the channel. This allows high-throughput dielectrophoretic cell separation in high conductivity, physiological-like fluids, overcoming the limitations of conventional dielectrophoresis. We demonstrate viable/non-viable separation efficacy of >98% in pre-purified mesenchymal stromal cells, extracted from human dental pulp, with no adverse effects on cell viability, or on their subsequent osteogenic capabilities.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Smith, Alban J.
O’Rorke, Richard D.
Kale, Akshay
Rimsa, Roberts
Tomlinson, Matthew J.
Kirkham, Jennifer
Davies, A. Giles
Wälti, Christoph
Wood, Christopher D.
format Article
author Smith, Alban J.
O’Rorke, Richard D.
Kale, Akshay
Rimsa, Roberts
Tomlinson, Matthew J.
Kirkham, Jennifer
Davies, A. Giles
Wälti, Christoph
Wood, Christopher D.
author_sort Smith, Alban J.
title Rapid cell separation with minimal manipulation for autologous cell therapies
title_short Rapid cell separation with minimal manipulation for autologous cell therapies
title_full Rapid cell separation with minimal manipulation for autologous cell therapies
title_fullStr Rapid cell separation with minimal manipulation for autologous cell therapies
title_full_unstemmed Rapid cell separation with minimal manipulation for autologous cell therapies
title_sort rapid cell separation with minimal manipulation for autologous cell therapies
publishDate 2018
url https://hdl.handle.net/10356/87589
http://hdl.handle.net/10220/45460
_version_ 1772826052417028096