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Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study

The purpose of this study is to assess the preclinical therapeutic efficacy of magnetic resonance imaging (MRI)-monitored focused ultrasound (FUS)-induced blood-brain barrier (BBB) disruption to enhance Temozolomide (TMZ) delivery for improving Glioblastoma Multiforme (GBM) treatment. MRI-monitored...

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Autores principales: Wei, Kuo-Chen, Chu, Po-Chun, Wang, Hay-Yan Jack, Huang, Chiung-Yin, Chen, Pin-Yuan, Tsai, Hong-Chieh, Lu, Yu-Jen, Lee, Pei-Yun, Tseng, I-Chou, Feng, Li-Ying, Hsu, Peng-Wei, Yen, Tzu-Chen, Liu, Hao-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602591/
https://www.ncbi.nlm.nih.gov/pubmed/23527068
http://dx.doi.org/10.1371/journal.pone.0058995
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author Wei, Kuo-Chen
Chu, Po-Chun
Wang, Hay-Yan Jack
Huang, Chiung-Yin
Chen, Pin-Yuan
Tsai, Hong-Chieh
Lu, Yu-Jen
Lee, Pei-Yun
Tseng, I-Chou
Feng, Li-Ying
Hsu, Peng-Wei
Yen, Tzu-Chen
Liu, Hao-Li
author_facet Wei, Kuo-Chen
Chu, Po-Chun
Wang, Hay-Yan Jack
Huang, Chiung-Yin
Chen, Pin-Yuan
Tsai, Hong-Chieh
Lu, Yu-Jen
Lee, Pei-Yun
Tseng, I-Chou
Feng, Li-Ying
Hsu, Peng-Wei
Yen, Tzu-Chen
Liu, Hao-Li
author_sort Wei, Kuo-Chen
collection PubMed
description The purpose of this study is to assess the preclinical therapeutic efficacy of magnetic resonance imaging (MRI)-monitored focused ultrasound (FUS)-induced blood-brain barrier (BBB) disruption to enhance Temozolomide (TMZ) delivery for improving Glioblastoma Multiforme (GBM) treatment. MRI-monitored FUS with microbubbles was used to transcranially disrupt the BBB in brains of Fisher rats implanted with 9L glioma cells. FUS-BBB opening was spectrophotometrically determined by leakage of dyes into the brain, and TMZ was quantitated in cerebrospinal fluid (CSF) and plasma by LC-MS\MS. The effects of treatment on tumor progression (by MRI), animal survival and brain tissue histology were investigated. Results demonstrated that FUS-BBB opening increased the local accumulation of dyes in brain parenchyma by 3.8-/2.1-fold in normal/tumor tissues. Compared to TMZ alone, combined FUS treatment increased the TMZ CSF/plasma ratio from 22.7% to 38.6%, reduced the 7-day tumor progression ratio from 24.03 to 5.06, and extended the median survival from 20 to 23 days. In conclusion, this study provided preclinical evidence that FUS BBB-opening increased the local concentration of TMZ to improve the control of tumor progression and animal survival, suggesting its clinical potential for improving current brain tumor treatment.
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spelling pubmed-36025912013-03-22 Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study Wei, Kuo-Chen Chu, Po-Chun Wang, Hay-Yan Jack Huang, Chiung-Yin Chen, Pin-Yuan Tsai, Hong-Chieh Lu, Yu-Jen Lee, Pei-Yun Tseng, I-Chou Feng, Li-Ying Hsu, Peng-Wei Yen, Tzu-Chen Liu, Hao-Li PLoS One Research Article The purpose of this study is to assess the preclinical therapeutic efficacy of magnetic resonance imaging (MRI)-monitored focused ultrasound (FUS)-induced blood-brain barrier (BBB) disruption to enhance Temozolomide (TMZ) delivery for improving Glioblastoma Multiforme (GBM) treatment. MRI-monitored FUS with microbubbles was used to transcranially disrupt the BBB in brains of Fisher rats implanted with 9L glioma cells. FUS-BBB opening was spectrophotometrically determined by leakage of dyes into the brain, and TMZ was quantitated in cerebrospinal fluid (CSF) and plasma by LC-MS\MS. The effects of treatment on tumor progression (by MRI), animal survival and brain tissue histology were investigated. Results demonstrated that FUS-BBB opening increased the local accumulation of dyes in brain parenchyma by 3.8-/2.1-fold in normal/tumor tissues. Compared to TMZ alone, combined FUS treatment increased the TMZ CSF/plasma ratio from 22.7% to 38.6%, reduced the 7-day tumor progression ratio from 24.03 to 5.06, and extended the median survival from 20 to 23 days. In conclusion, this study provided preclinical evidence that FUS BBB-opening increased the local concentration of TMZ to improve the control of tumor progression and animal survival, suggesting its clinical potential for improving current brain tumor treatment. Public Library of Science 2013-03-19 /pmc/articles/PMC3602591/ /pubmed/23527068 http://dx.doi.org/10.1371/journal.pone.0058995 Text en © 2013 Wei et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wei, Kuo-Chen
Chu, Po-Chun
Wang, Hay-Yan Jack
Huang, Chiung-Yin
Chen, Pin-Yuan
Tsai, Hong-Chieh
Lu, Yu-Jen
Lee, Pei-Yun
Tseng, I-Chou
Feng, Li-Ying
Hsu, Peng-Wei
Yen, Tzu-Chen
Liu, Hao-Li
Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study
title Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study
title_full Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study
title_fullStr Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study
title_full_unstemmed Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study
title_short Focused Ultrasound-Induced Blood–Brain Barrier Opening to Enhance Temozolomide Delivery for Glioblastoma Treatment: A Preclinical Study
title_sort focused ultrasound-induced blood–brain barrier opening to enhance temozolomide delivery for glioblastoma treatment: a preclinical study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602591/
https://www.ncbi.nlm.nih.gov/pubmed/23527068
http://dx.doi.org/10.1371/journal.pone.0058995
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