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Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption

Focused ultrasound combined with microbubble for blood-brain barrier disruption (FUS-BBBD) is a promising technique for noninvasive and localized brain drug delivery. This study demonstrates that passive cavitation imaging (PCI) is capable of predicting the location and concentration of nanoclusters...

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Autores principales: Yang, Yaoheng, Zhang, Xiaohui, Ye, Dezhuang, Laforest, Richard, Williamson, Jeffrey, Liu, Yongjian, Chen, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391404/
https://www.ncbi.nlm.nih.gov/pubmed/30808897
http://dx.doi.org/10.1038/s41598-019-39090-9
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author Yang, Yaoheng
Zhang, Xiaohui
Ye, Dezhuang
Laforest, Richard
Williamson, Jeffrey
Liu, Yongjian
Chen, Hong
author_facet Yang, Yaoheng
Zhang, Xiaohui
Ye, Dezhuang
Laforest, Richard
Williamson, Jeffrey
Liu, Yongjian
Chen, Hong
author_sort Yang, Yaoheng
collection PubMed
description Focused ultrasound combined with microbubble for blood-brain barrier disruption (FUS-BBBD) is a promising technique for noninvasive and localized brain drug delivery. This study demonstrates that passive cavitation imaging (PCI) is capable of predicting the location and concentration of nanoclusters delivered by FUS-BBBD. During FUS-BBBD treatment of mice, the acoustic emissions from FUS-activated microbubbles were passively detected by an ultrasound imaging system and processed offline using a frequency-domain PCI algorithm. After the FUS treatment, radiolabeled gold nanoclusters, (64)Cu-AuNCs, were intravenously injected into the mice and imaged by positron emission tomography/computed tomography (PET/CT). The centers of the stable cavitation dose (SCD) maps obtained by PCI and the corresponding centers of the (64)Cu-AuNCs concentration maps obtained by PET coincided within 0.3 ± 0.4 mm and 1.6 ± 1.1 mm in the transverse and axial directions of the FUS beam, respectively. The SCD maps were found to be linearly correlated with the (64)Cu-AuNCs concentration maps on a pixel-by-pixel level. These findings suggest that SCD maps can spatially “paint” the delivered nanocluster concentration, a technique that we named as cavitation dose painting. This PCI-based cavitation dose painting technique in combination with FUS-BBBD opens new horizons in spatially targeted and modulated brain drug delivery.
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spelling pubmed-63914042019-02-28 Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption Yang, Yaoheng Zhang, Xiaohui Ye, Dezhuang Laforest, Richard Williamson, Jeffrey Liu, Yongjian Chen, Hong Sci Rep Article Focused ultrasound combined with microbubble for blood-brain barrier disruption (FUS-BBBD) is a promising technique for noninvasive and localized brain drug delivery. This study demonstrates that passive cavitation imaging (PCI) is capable of predicting the location and concentration of nanoclusters delivered by FUS-BBBD. During FUS-BBBD treatment of mice, the acoustic emissions from FUS-activated microbubbles were passively detected by an ultrasound imaging system and processed offline using a frequency-domain PCI algorithm. After the FUS treatment, radiolabeled gold nanoclusters, (64)Cu-AuNCs, were intravenously injected into the mice and imaged by positron emission tomography/computed tomography (PET/CT). The centers of the stable cavitation dose (SCD) maps obtained by PCI and the corresponding centers of the (64)Cu-AuNCs concentration maps obtained by PET coincided within 0.3 ± 0.4 mm and 1.6 ± 1.1 mm in the transverse and axial directions of the FUS beam, respectively. The SCD maps were found to be linearly correlated with the (64)Cu-AuNCs concentration maps on a pixel-by-pixel level. These findings suggest that SCD maps can spatially “paint” the delivered nanocluster concentration, a technique that we named as cavitation dose painting. This PCI-based cavitation dose painting technique in combination with FUS-BBBD opens new horizons in spatially targeted and modulated brain drug delivery. Nature Publishing Group UK 2019-02-26 /pmc/articles/PMC6391404/ /pubmed/30808897 http://dx.doi.org/10.1038/s41598-019-39090-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yang, Yaoheng
Zhang, Xiaohui
Ye, Dezhuang
Laforest, Richard
Williamson, Jeffrey
Liu, Yongjian
Chen, Hong
Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
title Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
title_full Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
title_fullStr Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
title_full_unstemmed Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
title_short Cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
title_sort cavitation dose painting for focused ultrasound-induced blood-brain barrier disruption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391404/
https://www.ncbi.nlm.nih.gov/pubmed/30808897
http://dx.doi.org/10.1038/s41598-019-39090-9
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