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Nano to micro delivery systems: targeting angiogenesis in brain tumors

Treating brain tumors using inhibitors of angiogenesis is extensively researched and tested in clinical trials. Although anti-angiogenic treatment holds a great potential for treating primary and secondary brain tumors, no clinical treatment is currently approved for brain tumor patients. One of the...

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Detalles Bibliográficos
Autores principales: Gilert, Ariel, Machluf, Marcelle
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964525/
https://www.ncbi.nlm.nih.gov/pubmed/20932320
http://dx.doi.org/10.1186/2040-2384-2-20
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author Gilert, Ariel
Machluf, Marcelle
author_facet Gilert, Ariel
Machluf, Marcelle
author_sort Gilert, Ariel
collection PubMed
description Treating brain tumors using inhibitors of angiogenesis is extensively researched and tested in clinical trials. Although anti-angiogenic treatment holds a great potential for treating primary and secondary brain tumors, no clinical treatment is currently approved for brain tumor patients. One of the main hurdles in treating brain tumors is the blood brain barrier - a protective barrier of the brain, which prevents drugs from entering the brain parenchyma. As most therapeutics are excluded from the brain there is an urgent need to develop delivery platforms which will bypass such hurdles and enable the delivery of anti-angiogenic drugs into the tumor bed. Such delivery systems should be able to control release the drug or a combination of drugs at a therapeutic level for the desired time. In this mini-review we will discuss the latest improvements in nano and micro drug delivery platforms that were designed to deliver inhibitors of angiogenesis to the brain.
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spelling pubmed-29645252010-10-28 Nano to micro delivery systems: targeting angiogenesis in brain tumors Gilert, Ariel Machluf, Marcelle J Angiogenes Res Review Treating brain tumors using inhibitors of angiogenesis is extensively researched and tested in clinical trials. Although anti-angiogenic treatment holds a great potential for treating primary and secondary brain tumors, no clinical treatment is currently approved for brain tumor patients. One of the main hurdles in treating brain tumors is the blood brain barrier - a protective barrier of the brain, which prevents drugs from entering the brain parenchyma. As most therapeutics are excluded from the brain there is an urgent need to develop delivery platforms which will bypass such hurdles and enable the delivery of anti-angiogenic drugs into the tumor bed. Such delivery systems should be able to control release the drug or a combination of drugs at a therapeutic level for the desired time. In this mini-review we will discuss the latest improvements in nano and micro drug delivery platforms that were designed to deliver inhibitors of angiogenesis to the brain. BioMed Central 2010-10-08 /pmc/articles/PMC2964525/ /pubmed/20932320 http://dx.doi.org/10.1186/2040-2384-2-20 Text en Copyright ©2010 Gilert and Machluf; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Gilert, Ariel
Machluf, Marcelle
Nano to micro delivery systems: targeting angiogenesis in brain tumors
title Nano to micro delivery systems: targeting angiogenesis in brain tumors
title_full Nano to micro delivery systems: targeting angiogenesis in brain tumors
title_fullStr Nano to micro delivery systems: targeting angiogenesis in brain tumors
title_full_unstemmed Nano to micro delivery systems: targeting angiogenesis in brain tumors
title_short Nano to micro delivery systems: targeting angiogenesis in brain tumors
title_sort nano to micro delivery systems: targeting angiogenesis in brain tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964525/
https://www.ncbi.nlm.nih.gov/pubmed/20932320
http://dx.doi.org/10.1186/2040-2384-2-20
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