Drug and gene delivery across the blood-brain barrier with focused ultrasound.

Author: Timbie KF1, Mead BP1, Price RJ2
Affiliation:
1Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.
2Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA. Electronic address: rprice@virginia.edu.
Conference/Journal: J Control Release.
Date published: 2015 Dec 10
Other: Volume ID: 219 , Pages: 61-75 , Special Notes: doi: 10.1016/j.jconrel.2015.08.059. Epub 2015 Sep 8. , Word Count: 215


The blood-brain barrier (BBB) remains one of the most significant limitations to treatments of central nervous system (CNS) disorders including brain tumors, neurodegenerative diseases and psychiatric disorders. It is now well-established that focused ultrasound (FUS) in conjunction with contrast agent microbubbles may be used to non-invasively and temporarily disrupt the BBB, allowing localized delivery of systemically administered therapeutic agents as large as 100nm in size to the CNS. Importantly, recent technological advances now permit FUS application through the intact human skull, obviating the need for invasive and risky surgical procedures. When used in combination with magnetic resonance imaging, FUS may be applied precisely to pre-selected CNS targets. Indeed, FUS devices capable of sub-millimeter precision are currently in several clinical trials. FUS mediated BBB disruption has the potential to fundamentally change how CNS diseases are treated, unlocking potential for combinatorial treatments with nanotechnology, markedly increasing the efficacy of existing therapeutics that otherwise do not cross the BBB effectively, and permitting safe repeated treatments. This article comprehensively reviews recent studies on the targeted delivery of therapeutics into the CNS with FUS and offers perspectives on the future of this technology.

Copyright © 2015 Elsevier B.V. All rights reserved.

KEYWORDS: Blood–brain barrier; CNS drug delivery; Focused ultrasound; Nanoparticles

PMID: 26362698 PMCID: PMC4656107 [Available on 2016-12-10] DOI: 10.1016/j.jconrel.2015.08.059

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