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A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation

Isolation of cells and their transfection in a controlled manner is an integral step in cell biotechnology. Electric field approaches such as dielectrophoresis (DEP) offers a more viable method for targeted immobilization of cells without any labels. For transfection of cells to incorporate exogenou...

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Autores principales: Punjiya, Meera, Nejad, Hojatollah Rezaei, Mathews, Juanita, Levin, Michael, Sonkusale, Sameer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700080/
https://www.ncbi.nlm.nih.gov/pubmed/31427614
http://dx.doi.org/10.1038/s41598-019-48198-x
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author Punjiya, Meera
Nejad, Hojatollah Rezaei
Mathews, Juanita
Levin, Michael
Sonkusale, Sameer
author_facet Punjiya, Meera
Nejad, Hojatollah Rezaei
Mathews, Juanita
Levin, Michael
Sonkusale, Sameer
author_sort Punjiya, Meera
collection PubMed
description Isolation of cells and their transfection in a controlled manner is an integral step in cell biotechnology. Electric field approaches such as dielectrophoresis (DEP) offers a more viable method for targeted immobilization of cells without any labels. For transfection of cells to incorporate exogenous materials, electrical methods such as electroporation, are preferred over chemical and viral delivery methods since they minimally affect cell viability and can target many types. However prior approaches to both methods required multiple excitation sources, an AC source for DEP-based trapping and another DC source for electroporation. In this paper, we present a first of its kind flow through lab-on-chip platform using a single AC excitation source for combined trapping using negative dielectrophoresis (nDEP) and AC electroporation. Use of AC fields for electroporation eliminates the unwanted side effects of electrolysis or joule heating at electrodes compared to DC electroporation. Adjusting the flow rate and the electrical parameters of the incident AC field precisely controls the operation (trap, trap with electroporation and release). The platform has been validated through trapping and simultaneous transfection of HEK-293 embryonic kidney cells with a plasmid vector containing a fluorescent protein tag. Numerical scaling analysis is provided that indicates promise for individual cell trapping and electroporation using low voltage AC fields.
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spelling pubmed-67000802019-08-21 A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation Punjiya, Meera Nejad, Hojatollah Rezaei Mathews, Juanita Levin, Michael Sonkusale, Sameer Sci Rep Article Isolation of cells and their transfection in a controlled manner is an integral step in cell biotechnology. Electric field approaches such as dielectrophoresis (DEP) offers a more viable method for targeted immobilization of cells without any labels. For transfection of cells to incorporate exogenous materials, electrical methods such as electroporation, are preferred over chemical and viral delivery methods since they minimally affect cell viability and can target many types. However prior approaches to both methods required multiple excitation sources, an AC source for DEP-based trapping and another DC source for electroporation. In this paper, we present a first of its kind flow through lab-on-chip platform using a single AC excitation source for combined trapping using negative dielectrophoresis (nDEP) and AC electroporation. Use of AC fields for electroporation eliminates the unwanted side effects of electrolysis or joule heating at electrodes compared to DC electroporation. Adjusting the flow rate and the electrical parameters of the incident AC field precisely controls the operation (trap, trap with electroporation and release). The platform has been validated through trapping and simultaneous transfection of HEK-293 embryonic kidney cells with a plasmid vector containing a fluorescent protein tag. Numerical scaling analysis is provided that indicates promise for individual cell trapping and electroporation using low voltage AC fields. Nature Publishing Group UK 2019-08-19 /pmc/articles/PMC6700080/ /pubmed/31427614 http://dx.doi.org/10.1038/s41598-019-48198-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Punjiya, Meera
Nejad, Hojatollah Rezaei
Mathews, Juanita
Levin, Michael
Sonkusale, Sameer
A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation
title A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation
title_full A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation
title_fullStr A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation
title_full_unstemmed A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation
title_short A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation
title_sort flow through device for simultaneous dielectrophoretic cell trapping and ac electroporation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700080/
https://www.ncbi.nlm.nih.gov/pubmed/31427614
http://dx.doi.org/10.1038/s41598-019-48198-x
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