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Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation
Treatment of intracranial disorders suffers from the inability to accumulate therapeutic drug concentrations due to protection from the blood–brain barrier (BBB). Electroporation-based therapies have demonstrated the capability of permeating the BBB, but knowledge of the longevity of BBB disruption...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966593/ https://www.ncbi.nlm.nih.gov/pubmed/31771214 http://dx.doi.org/10.3390/cancers11121850 |
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author | Lorenzo, Melvin F. Thomas, Sean C. Kani, Yukitaka Hinckley, Jonathan Lee, Matthew Adler, Joy Verbridge, Scott S. Hsu, Fang-Chi Robertson, John L. Davalos, Rafael V. Rossmeisl, John H. |
author_facet | Lorenzo, Melvin F. Thomas, Sean C. Kani, Yukitaka Hinckley, Jonathan Lee, Matthew Adler, Joy Verbridge, Scott S. Hsu, Fang-Chi Robertson, John L. Davalos, Rafael V. Rossmeisl, John H. |
author_sort | Lorenzo, Melvin F. |
collection | PubMed |
description | Treatment of intracranial disorders suffers from the inability to accumulate therapeutic drug concentrations due to protection from the blood–brain barrier (BBB). Electroporation-based therapies have demonstrated the capability of permeating the BBB, but knowledge of the longevity of BBB disruption (BBBD) is limited. In this study, we quantify the temporal, high-frequency electroporation (HFE)-mediated BBBD in an in vivo healthy rat brain model. 40 male Fisher rats underwent HFE treatment; two blunt tipped monopolar electrodes were advanced into the brain and 200 bursts of HFE were delivered at a voltage-to-distance ratio of 600 V/cm. BBBD was verified with contrast enhanced T1W MRI (gadopentetate dimeglumine) and pathologically (Evans blue dye) at time points of 1, 24, 48, 72, and 96 h after HFE. Contrast enhanced T1W scans demonstrated BBBD for 1 to 72 h after HFE but intact BBB at 96 h. Histologically, tissue damage was restricted to electrode insertion tracks. BBBD was induced with minimal muscle contractions and minimal cell death attributed to HFE. Numerical modeling indicated that brief BBBD was induced with low magnitude electric fields, and BBBD duration increased with field strength. These data suggest the spatiotemporal characteristics of HFE-mediated BBBD may be modulated with the locally applied electric field. |
format | Online Article Text |
id | pubmed-6966593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69665932020-02-04 Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation Lorenzo, Melvin F. Thomas, Sean C. Kani, Yukitaka Hinckley, Jonathan Lee, Matthew Adler, Joy Verbridge, Scott S. Hsu, Fang-Chi Robertson, John L. Davalos, Rafael V. Rossmeisl, John H. Cancers (Basel) Article Treatment of intracranial disorders suffers from the inability to accumulate therapeutic drug concentrations due to protection from the blood–brain barrier (BBB). Electroporation-based therapies have demonstrated the capability of permeating the BBB, but knowledge of the longevity of BBB disruption (BBBD) is limited. In this study, we quantify the temporal, high-frequency electroporation (HFE)-mediated BBBD in an in vivo healthy rat brain model. 40 male Fisher rats underwent HFE treatment; two blunt tipped monopolar electrodes were advanced into the brain and 200 bursts of HFE were delivered at a voltage-to-distance ratio of 600 V/cm. BBBD was verified with contrast enhanced T1W MRI (gadopentetate dimeglumine) and pathologically (Evans blue dye) at time points of 1, 24, 48, 72, and 96 h after HFE. Contrast enhanced T1W scans demonstrated BBBD for 1 to 72 h after HFE but intact BBB at 96 h. Histologically, tissue damage was restricted to electrode insertion tracks. BBBD was induced with minimal muscle contractions and minimal cell death attributed to HFE. Numerical modeling indicated that brief BBBD was induced with low magnitude electric fields, and BBBD duration increased with field strength. These data suggest the spatiotemporal characteristics of HFE-mediated BBBD may be modulated with the locally applied electric field. MDPI 2019-11-23 /pmc/articles/PMC6966593/ /pubmed/31771214 http://dx.doi.org/10.3390/cancers11121850 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lorenzo, Melvin F. Thomas, Sean C. Kani, Yukitaka Hinckley, Jonathan Lee, Matthew Adler, Joy Verbridge, Scott S. Hsu, Fang-Chi Robertson, John L. Davalos, Rafael V. Rossmeisl, John H. Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation |
title | Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation |
title_full | Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation |
title_fullStr | Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation |
title_full_unstemmed | Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation |
title_short | Temporal Characterization of Blood–Brain Barrier Disruption with High-Frequency Electroporation |
title_sort | temporal characterization of blood–brain barrier disruption with high-frequency electroporation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966593/ https://www.ncbi.nlm.nih.gov/pubmed/31771214 http://dx.doi.org/10.3390/cancers11121850 |
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