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Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure

The mechanism(s) responsible for the breakdown (nanoporation) of cell plasma membranes after nanosecond pulse (nsEP) exposure remains poorly understood. Current theories focus exclusively on the electrical field, citing electrostriction, water dipole alignment and/or electrodeformation as the primar...

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Autores principales: Roth, Caleb C., Barnes Jr., Ronald A., Ibey, Bennett L., Beier, Hope T., Christopher Mimun, L., Maswadi, Saher M., Shadaram, Mehdi, Glickman, Randolph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598730/
https://www.ncbi.nlm.nih.gov/pubmed/26450165
http://dx.doi.org/10.1038/srep15063
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author Roth, Caleb C.
Barnes Jr., Ronald A.
Ibey, Bennett L.
Beier, Hope T.
Christopher Mimun, L.
Maswadi, Saher M.
Shadaram, Mehdi
Glickman, Randolph D.
author_facet Roth, Caleb C.
Barnes Jr., Ronald A.
Ibey, Bennett L.
Beier, Hope T.
Christopher Mimun, L.
Maswadi, Saher M.
Shadaram, Mehdi
Glickman, Randolph D.
author_sort Roth, Caleb C.
collection PubMed
description The mechanism(s) responsible for the breakdown (nanoporation) of cell plasma membranes after nanosecond pulse (nsEP) exposure remains poorly understood. Current theories focus exclusively on the electrical field, citing electrostriction, water dipole alignment and/or electrodeformation as the primary mechanisms for pore formation. However, the delivery of a high-voltage nsEP to cells by tungsten electrodes creates a multitude of biophysical phenomena, including electrohydraulic cavitation, electrochemical interactions, thermoelastic expansion, and others. To date, very limited research has investigated non-electric phenomena occurring during nsEP exposures and their potential effect on cell nanoporation. Of primary interest is the production of acoustic shock waves during nsEP exposure, as it is known that acoustic shock waves can cause membrane poration (sonoporation). Based on these observations, our group characterized the acoustic pressure transients generated by nsEP and determined if such transients played any role in nanoporation. In this paper, we show that nsEP exposures, equivalent to those used in cellular studies, are capable of generating high-frequency (2.5 MHz), high-intensity (>13 kPa) pressure transients. Using confocal microscopy to measure cell uptake of YO-PRO®-1 (indicator of nanoporation of the plasma membrane) and changing the electrode geometry, we determined that acoustic waves alone are not responsible for poration of the membrane.
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spelling pubmed-45987302015-10-13 Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure Roth, Caleb C. Barnes Jr., Ronald A. Ibey, Bennett L. Beier, Hope T. Christopher Mimun, L. Maswadi, Saher M. Shadaram, Mehdi Glickman, Randolph D. Sci Rep Article The mechanism(s) responsible for the breakdown (nanoporation) of cell plasma membranes after nanosecond pulse (nsEP) exposure remains poorly understood. Current theories focus exclusively on the electrical field, citing electrostriction, water dipole alignment and/or electrodeformation as the primary mechanisms for pore formation. However, the delivery of a high-voltage nsEP to cells by tungsten electrodes creates a multitude of biophysical phenomena, including electrohydraulic cavitation, electrochemical interactions, thermoelastic expansion, and others. To date, very limited research has investigated non-electric phenomena occurring during nsEP exposures and their potential effect on cell nanoporation. Of primary interest is the production of acoustic shock waves during nsEP exposure, as it is known that acoustic shock waves can cause membrane poration (sonoporation). Based on these observations, our group characterized the acoustic pressure transients generated by nsEP and determined if such transients played any role in nanoporation. In this paper, we show that nsEP exposures, equivalent to those used in cellular studies, are capable of generating high-frequency (2.5 MHz), high-intensity (>13 kPa) pressure transients. Using confocal microscopy to measure cell uptake of YO-PRO®-1 (indicator of nanoporation of the plasma membrane) and changing the electrode geometry, we determined that acoustic waves alone are not responsible for poration of the membrane. Nature Publishing Group 2015-10-09 /pmc/articles/PMC4598730/ /pubmed/26450165 http://dx.doi.org/10.1038/srep15063 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ 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/
spellingShingle Article
Roth, Caleb C.
Barnes Jr., Ronald A.
Ibey, Bennett L.
Beier, Hope T.
Christopher Mimun, L.
Maswadi, Saher M.
Shadaram, Mehdi
Glickman, Randolph D.
Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure
title Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure
title_full Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure
title_fullStr Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure
title_full_unstemmed Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure
title_short Characterization of Pressure Transients Generated by Nanosecond Electrical Pulse (nsEP) Exposure
title_sort characterization of pressure transients generated by nanosecond electrical pulse (nsep) exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598730/
https://www.ncbi.nlm.nih.gov/pubmed/26450165
http://dx.doi.org/10.1038/srep15063
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