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Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)

BACKGROUND: Percutaneous image-guided tissue ablation (IGA) plays a growing role in the clinical management of solid malignancies. Electroporation is used for IGA in several modalities: irreversible electroporation (IRE), and reversible electroporation with chemotoxic drugs, called electrochemothera...

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Autores principales: Guenther, Enric, Klein, Nina, Mikus, Paul, Botea, Florin, Pautov, Mihail, Lugnani, Franco, Macchioro, Matteo, Popescu, Irinel, Stehling, Michael K., Rubinsky, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977482/
https://www.ncbi.nlm.nih.gov/pubmed/31998549
http://dx.doi.org/10.7717/peerj.7985
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author Guenther, Enric
Klein, Nina
Mikus, Paul
Botea, Florin
Pautov, Mihail
Lugnani, Franco
Macchioro, Matteo
Popescu, Irinel
Stehling, Michael K.
Rubinsky, Boris
author_facet Guenther, Enric
Klein, Nina
Mikus, Paul
Botea, Florin
Pautov, Mihail
Lugnani, Franco
Macchioro, Matteo
Popescu, Irinel
Stehling, Michael K.
Rubinsky, Boris
author_sort Guenther, Enric
collection PubMed
description BACKGROUND: Percutaneous image-guided tissue ablation (IGA) plays a growing role in the clinical management of solid malignancies. Electroporation is used for IGA in several modalities: irreversible electroporation (IRE), and reversible electroporation with chemotoxic drugs, called electrochemotherapy (ECT). It was shown that the combination of electrolysis and electroporation—E2—affords tissue ablation with greater efficiency, that is, lower voltages, lower energy and shorter procedure times than IRE and without the need for chemotoxic additives as in ECT. METHODS: A new E2 waveform was designed that delivers optimal doses of electroporation and electrolysis in a single waveform. A series of experiments were performed in the liver of pigs to evaluate E2 in the context of clinical applications. The goal was to find initial parameter boundaries in terms of electrical field, pulse duration and charge as well as tissue behavior to enable real time tissue ablation of clinically relevant volumes. RESULTS: Histological results show that a single several hundred millisecond long E2 waveform can ablate large volume of tissue at relatively low voltages while preserving the integrity of large blood vessels and lumen structures in the ablation zone without the use of chemotoxic drugs or paralyzing drugs during anesthesia. This could translate clinically into much shorter treatment times and ease of use compared to other techniques that are currently applied.
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spelling pubmed-69774822020-01-29 Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2) Guenther, Enric Klein, Nina Mikus, Paul Botea, Florin Pautov, Mihail Lugnani, Franco Macchioro, Matteo Popescu, Irinel Stehling, Michael K. Rubinsky, Boris PeerJ Biophysics BACKGROUND: Percutaneous image-guided tissue ablation (IGA) plays a growing role in the clinical management of solid malignancies. Electroporation is used for IGA in several modalities: irreversible electroporation (IRE), and reversible electroporation with chemotoxic drugs, called electrochemotherapy (ECT). It was shown that the combination of electrolysis and electroporation—E2—affords tissue ablation with greater efficiency, that is, lower voltages, lower energy and shorter procedure times than IRE and without the need for chemotoxic additives as in ECT. METHODS: A new E2 waveform was designed that delivers optimal doses of electroporation and electrolysis in a single waveform. A series of experiments were performed in the liver of pigs to evaluate E2 in the context of clinical applications. The goal was to find initial parameter boundaries in terms of electrical field, pulse duration and charge as well as tissue behavior to enable real time tissue ablation of clinically relevant volumes. RESULTS: Histological results show that a single several hundred millisecond long E2 waveform can ablate large volume of tissue at relatively low voltages while preserving the integrity of large blood vessels and lumen structures in the ablation zone without the use of chemotoxic drugs or paralyzing drugs during anesthesia. This could translate clinically into much shorter treatment times and ease of use compared to other techniques that are currently applied. PeerJ Inc. 2020-01-20 /pmc/articles/PMC6977482/ /pubmed/31998549 http://dx.doi.org/10.7717/peerj.7985 Text en © 2020 Gunther et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biophysics
Guenther, Enric
Klein, Nina
Mikus, Paul
Botea, Florin
Pautov, Mihail
Lugnani, Franco
Macchioro, Matteo
Popescu, Irinel
Stehling, Michael K.
Rubinsky, Boris
Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)
title Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)
title_full Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)
title_fullStr Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)
title_full_unstemmed Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)
title_short Toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (E2)
title_sort toward a clinical real time tissue ablation technology: combining electroporation and electrolysis (e2)
topic Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977482/
https://www.ncbi.nlm.nih.gov/pubmed/31998549
http://dx.doi.org/10.7717/peerj.7985
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