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Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound

PURPOSE: The purpose of this study was to evaluate the permeability of the blood–brain barrier after sonication by pulsed high-intensity focused ultrasound and to determine if such an approach increases the tumor:ipsilateral brain permeability ratio. MATERIALS AND METHODS: F98 glioma-bearing Fischer...

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Autores principales: Yang, Feng-Yi, Wang, Hsin-Ell, Lin, Guan-Liang, Lin, Hui-Hsien, Wong, Tai-Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282611/
https://www.ncbi.nlm.nih.gov/pubmed/22359451
http://dx.doi.org/10.2147/IJN.S28503
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author Yang, Feng-Yi
Wang, Hsin-Ell
Lin, Guan-Liang
Lin, Hui-Hsien
Wong, Tai-Tong
author_facet Yang, Feng-Yi
Wang, Hsin-Ell
Lin, Guan-Liang
Lin, Hui-Hsien
Wong, Tai-Tong
author_sort Yang, Feng-Yi
collection PubMed
description PURPOSE: The purpose of this study was to evaluate the permeability of the blood–brain barrier after sonication by pulsed high-intensity focused ultrasound and to determine if such an approach increases the tumor:ipsilateral brain permeability ratio. MATERIALS AND METHODS: F98 glioma-bearing Fischer 344 rats were injected intravenously with Evans blue with or without blood–tumor barrier disruption induced by transcranial pulsed high-intensity focused ultrasound. Sonication was applied at a frequency of 1 MHz with a 5% duty cycle and a repetition frequency of 1 Hz. The permeability of the blood–brain barrier was assessed by the extravasation of Evans blue. Contrast-enhanced magnetic resonance images were used to monitor the gadolinium deposition path associated with transcranial pulsed high-intensity focused ultrasound, and the influencing size and location was also investigated. In addition, whole brain histological analysis was performed. The results were compared by two-tailed unpaired t-test. RESULTS: The accumulation of Evans blue in brains and the tumor:ipsilateral brain permeability ratio of Evans blue were significantly increased after pulsed high-intensity focused ultrasound exposure. Evans blue injection followed by sonication showed an increase in the tumor:ipsilateral brain ratio of the target tumors (9.14:1) of about 2.23-fold compared with the control tumors (x4.09) on day 6 after tumor implantation. Magnetic resonance images showed that pulsed high-intensity focused ultrasound locally enhances the permeability of the blood–tumor barrier in the glioma-bearing rats. CONCLUSION: This method could allow enhanced synergistic effects with respect to other brain tumor treatment regimens.
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spelling pubmed-32826112012-02-22 Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound Yang, Feng-Yi Wang, Hsin-Ell Lin, Guan-Liang Lin, Hui-Hsien Wong, Tai-Tong Int J Nanomedicine Original Research PURPOSE: The purpose of this study was to evaluate the permeability of the blood–brain barrier after sonication by pulsed high-intensity focused ultrasound and to determine if such an approach increases the tumor:ipsilateral brain permeability ratio. MATERIALS AND METHODS: F98 glioma-bearing Fischer 344 rats were injected intravenously with Evans blue with or without blood–tumor barrier disruption induced by transcranial pulsed high-intensity focused ultrasound. Sonication was applied at a frequency of 1 MHz with a 5% duty cycle and a repetition frequency of 1 Hz. The permeability of the blood–brain barrier was assessed by the extravasation of Evans blue. Contrast-enhanced magnetic resonance images were used to monitor the gadolinium deposition path associated with transcranial pulsed high-intensity focused ultrasound, and the influencing size and location was also investigated. In addition, whole brain histological analysis was performed. The results were compared by two-tailed unpaired t-test. RESULTS: The accumulation of Evans blue in brains and the tumor:ipsilateral brain permeability ratio of Evans blue were significantly increased after pulsed high-intensity focused ultrasound exposure. Evans blue injection followed by sonication showed an increase in the tumor:ipsilateral brain ratio of the target tumors (9.14:1) of about 2.23-fold compared with the control tumors (x4.09) on day 6 after tumor implantation. Magnetic resonance images showed that pulsed high-intensity focused ultrasound locally enhances the permeability of the blood–tumor barrier in the glioma-bearing rats. CONCLUSION: This method could allow enhanced synergistic effects with respect to other brain tumor treatment regimens. Dove Medical Press 2012 2012-02-13 /pmc/articles/PMC3282611/ /pubmed/22359451 http://dx.doi.org/10.2147/IJN.S28503 Text en © 2012 Yang et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Yang, Feng-Yi
Wang, Hsin-Ell
Lin, Guan-Liang
Lin, Hui-Hsien
Wong, Tai-Tong
Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
title Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
title_full Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
title_fullStr Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
title_full_unstemmed Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
title_short Evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
title_sort evaluation of the increase in permeability of the blood–brain barrier during tumor progression after pulsed focused ultrasound
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282611/
https://www.ncbi.nlm.nih.gov/pubmed/22359451
http://dx.doi.org/10.2147/IJN.S28503
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