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Strategies for the enhanced intracellular delivery of nanomaterials

The intracellular delivery of nanomaterials and drugs has been attracting increasing research interest, mainly because of their important effects and functions in several organelles. Targeting specific organelles can help treat or decrease the symptoms of diabetes, cancer, infectious, and autoimmune...

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Detalles Bibliográficos
Autores principales: Azevedo, Cláudia, Macedo, Maria Helena, Sarmento, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108348/
https://www.ncbi.nlm.nih.gov/pubmed/28919437
http://dx.doi.org/10.1016/j.drudis.2017.08.011
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author Azevedo, Cláudia
Macedo, Maria Helena
Sarmento, Bruno
author_facet Azevedo, Cláudia
Macedo, Maria Helena
Sarmento, Bruno
author_sort Azevedo, Cláudia
collection PubMed
description The intracellular delivery of nanomaterials and drugs has been attracting increasing research interest, mainly because of their important effects and functions in several organelles. Targeting specific organelles can help treat or decrease the symptoms of diabetes, cancer, infectious, and autoimmune diseases. Tuning biological and chemical properties enables the creation of functionalized nanomaterials with enhanced intracellular uptake, ability to escape premature lysosome degradation, and to reach a specific target. Here, we provide an update of recent advances in the intracellular delivery mechanisms that could help drugs reach their target more efficiently.
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spelling pubmed-71083482020-03-31 Strategies for the enhanced intracellular delivery of nanomaterials Azevedo, Cláudia Macedo, Maria Helena Sarmento, Bruno Drug Discov Today Article The intracellular delivery of nanomaterials and drugs has been attracting increasing research interest, mainly because of their important effects and functions in several organelles. Targeting specific organelles can help treat or decrease the symptoms of diabetes, cancer, infectious, and autoimmune diseases. Tuning biological and chemical properties enables the creation of functionalized nanomaterials with enhanced intracellular uptake, ability to escape premature lysosome degradation, and to reach a specific target. Here, we provide an update of recent advances in the intracellular delivery mechanisms that could help drugs reach their target more efficiently. Elsevier Ltd. 2018-05 2017-09-15 /pmc/articles/PMC7108348/ /pubmed/28919437 http://dx.doi.org/10.1016/j.drudis.2017.08.011 Text en © 2017 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Azevedo, Cláudia
Macedo, Maria Helena
Sarmento, Bruno
Strategies for the enhanced intracellular delivery of nanomaterials
title Strategies for the enhanced intracellular delivery of nanomaterials
title_full Strategies for the enhanced intracellular delivery of nanomaterials
title_fullStr Strategies for the enhanced intracellular delivery of nanomaterials
title_full_unstemmed Strategies for the enhanced intracellular delivery of nanomaterials
title_short Strategies for the enhanced intracellular delivery of nanomaterials
title_sort strategies for the enhanced intracellular delivery of nanomaterials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108348/
https://www.ncbi.nlm.nih.gov/pubmed/28919437
http://dx.doi.org/10.1016/j.drudis.2017.08.011
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