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Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery

The blood–brain barrier (BBB) is formed by brain microvascular endothelial cells that are sealed by tight junctions, making it a significant obstacle for most brain therapeutics. The poor BBB penetration of newly developed therapeutics has therefore played a major role in limiting their clinical suc...

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Detalles Bibliográficos
Autores principales: Luo, Huilong, Shusta, Eric V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697580/
https://www.ncbi.nlm.nih.gov/pubmed/33198244
http://dx.doi.org/10.3390/pharmaceutics12111085
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author Luo, Huilong
Shusta, Eric V.
author_facet Luo, Huilong
Shusta, Eric V.
author_sort Luo, Huilong
collection PubMed
description The blood–brain barrier (BBB) is formed by brain microvascular endothelial cells that are sealed by tight junctions, making it a significant obstacle for most brain therapeutics. The poor BBB penetration of newly developed therapeutics has therefore played a major role in limiting their clinical success. A particularly challenging therapeutic target is glioma, which is the most frequently occurring malignant brain tumor. Thus, to enhance therapeutic uptake in tumors, researchers have been developing strategies to modulate BBB permeability. However, most conventional BBB opening strategies are difficult to apply in the clinical setting due to their broad, non-specific modulation of the BBB, which can result in damage to normal brain tissue. In this review, we have summarized strategies that could potentially be used to selectively and efficiently modulate the tumor BBB for more effective glioma treatment.
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spelling pubmed-76975802020-11-29 Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery Luo, Huilong Shusta, Eric V. Pharmaceutics Review The blood–brain barrier (BBB) is formed by brain microvascular endothelial cells that are sealed by tight junctions, making it a significant obstacle for most brain therapeutics. The poor BBB penetration of newly developed therapeutics has therefore played a major role in limiting their clinical success. A particularly challenging therapeutic target is glioma, which is the most frequently occurring malignant brain tumor. Thus, to enhance therapeutic uptake in tumors, researchers have been developing strategies to modulate BBB permeability. However, most conventional BBB opening strategies are difficult to apply in the clinical setting due to their broad, non-specific modulation of the BBB, which can result in damage to normal brain tissue. In this review, we have summarized strategies that could potentially be used to selectively and efficiently modulate the tumor BBB for more effective glioma treatment. MDPI 2020-11-12 /pmc/articles/PMC7697580/ /pubmed/33198244 http://dx.doi.org/10.3390/pharmaceutics12111085 Text en © 2020 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 Review
Luo, Huilong
Shusta, Eric V.
Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery
title Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery
title_full Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery
title_fullStr Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery
title_full_unstemmed Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery
title_short Blood–Brain Barrier Modulation to Improve Glioma Drug Delivery
title_sort blood–brain barrier modulation to improve glioma drug delivery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697580/
https://www.ncbi.nlm.nih.gov/pubmed/33198244
http://dx.doi.org/10.3390/pharmaceutics12111085
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