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Targeted Theranostic Nanoparticles for Brain Tumor Treatment

The poor prognosis and rapid recurrence of glioblastoma (GB) are associated to its fast-growing process and invasive nature, which make difficult the complete removal of the cancer infiltrated tissues. Additionally, GB heterogeneity within and between patients demands a patient-focused method of tre...

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Autores principales: Mendes, Maria, Sousa, João José, Pais, Alberto, Vitorino, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321593/
https://www.ncbi.nlm.nih.gov/pubmed/30304861
http://dx.doi.org/10.3390/pharmaceutics10040181
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author Mendes, Maria
Sousa, João José
Pais, Alberto
Vitorino, Carla
author_facet Mendes, Maria
Sousa, João José
Pais, Alberto
Vitorino, Carla
author_sort Mendes, Maria
collection PubMed
description The poor prognosis and rapid recurrence of glioblastoma (GB) are associated to its fast-growing process and invasive nature, which make difficult the complete removal of the cancer infiltrated tissues. Additionally, GB heterogeneity within and between patients demands a patient-focused method of treatment. Thus, the implementation of nanotechnology is an attractive approach considering all anatomic issues of GB, since it will potentially improve brain drug distribution, due to the interaction between the blood–brain barrier and nanoparticles (NPs). In recent years, theranostic techniques have also been proposed and regarded as promising. NPs are advantageous for this application, due to their respective size, easy surface modification and versatility to integrate multiple functional components in one system. The design of nanoparticles focused on therapeutic and diagnostic applications has increased exponentially for the treatment of cancer. This dual approach helps to understand the location of the tumor tissue, the biodistribution of nanoparticles, the progress and efficacy of the treatment, and is highly useful for personalized medicine-based therapeutic interventions. To improve theranostic approaches, different active strategies can be used to modulate the surface of the nanotheranostic particle, including surface markers, proteins, drugs or genes, and take advantage of the characteristics of the microenvironment using stimuli responsive triggers. This review focuses on the different strategies to improve the GB treatment, describing some cell surface markers and their ligands, and reports some strategies, and their efficacy, used in the current research.
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spelling pubmed-63215932019-01-11 Targeted Theranostic Nanoparticles for Brain Tumor Treatment Mendes, Maria Sousa, João José Pais, Alberto Vitorino, Carla Pharmaceutics Review The poor prognosis and rapid recurrence of glioblastoma (GB) are associated to its fast-growing process and invasive nature, which make difficult the complete removal of the cancer infiltrated tissues. Additionally, GB heterogeneity within and between patients demands a patient-focused method of treatment. Thus, the implementation of nanotechnology is an attractive approach considering all anatomic issues of GB, since it will potentially improve brain drug distribution, due to the interaction between the blood–brain barrier and nanoparticles (NPs). In recent years, theranostic techniques have also been proposed and regarded as promising. NPs are advantageous for this application, due to their respective size, easy surface modification and versatility to integrate multiple functional components in one system. The design of nanoparticles focused on therapeutic and diagnostic applications has increased exponentially for the treatment of cancer. This dual approach helps to understand the location of the tumor tissue, the biodistribution of nanoparticles, the progress and efficacy of the treatment, and is highly useful for personalized medicine-based therapeutic interventions. To improve theranostic approaches, different active strategies can be used to modulate the surface of the nanotheranostic particle, including surface markers, proteins, drugs or genes, and take advantage of the characteristics of the microenvironment using stimuli responsive triggers. This review focuses on the different strategies to improve the GB treatment, describing some cell surface markers and their ligands, and reports some strategies, and their efficacy, used in the current research. MDPI 2018-10-09 /pmc/articles/PMC6321593/ /pubmed/30304861 http://dx.doi.org/10.3390/pharmaceutics10040181 Text en © 2018 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
Mendes, Maria
Sousa, João José
Pais, Alberto
Vitorino, Carla
Targeted Theranostic Nanoparticles for Brain Tumor Treatment
title Targeted Theranostic Nanoparticles for Brain Tumor Treatment
title_full Targeted Theranostic Nanoparticles for Brain Tumor Treatment
title_fullStr Targeted Theranostic Nanoparticles for Brain Tumor Treatment
title_full_unstemmed Targeted Theranostic Nanoparticles for Brain Tumor Treatment
title_short Targeted Theranostic Nanoparticles for Brain Tumor Treatment
title_sort targeted theranostic nanoparticles for brain tumor treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321593/
https://www.ncbi.nlm.nih.gov/pubmed/30304861
http://dx.doi.org/10.3390/pharmaceutics10040181
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