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Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance

Chemotherapy is still a main option for cancer therapy, but its efficacy is often unsatisfying due to multidrug resistance (MDR). The tumor microenvironment is considered a dominant factor causing MDR. Stimuli-responsive nanomedicines exhibit many superiorities for reversal of MDR. As smart systems,...

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Detalles Bibliográficos
Autores principales: Zhou, Lei, Wang, Hao, Li, Yaping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817110/
https://www.ncbi.nlm.nih.gov/pubmed/29463999
http://dx.doi.org/10.7150/thno.22679
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author Zhou, Lei
Wang, Hao
Li, Yaping
author_facet Zhou, Lei
Wang, Hao
Li, Yaping
author_sort Zhou, Lei
collection PubMed
description Chemotherapy is still a main option for cancer therapy, but its efficacy is often unsatisfying due to multidrug resistance (MDR). The tumor microenvironment is considered a dominant factor causing MDR. Stimuli-responsive nanomedicines exhibit many superiorities for reversal of MDR. As smart systems, stimuli-responsive nanomedicines are desirable for achieving site-specific accumulation and triggered drug release in response to slight changes in physicochemical properties in pathological conditions or to exogenous stimuli. In this review, we highlight the current progress of various nanomedicines with different stimuli-responsive capabilities for overcoming MDR. The materials, design, construction as well as efficacy in overcoming MDR of these nanomedicines are discussed. Eventually, we look forward to forthcoming intelligent nanoparticle systems with new mechanisms to deliver drugs for practical applications in conquering cancer MDR.
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spelling pubmed-58171102018-02-20 Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance Zhou, Lei Wang, Hao Li, Yaping Theranostics Review Chemotherapy is still a main option for cancer therapy, but its efficacy is often unsatisfying due to multidrug resistance (MDR). The tumor microenvironment is considered a dominant factor causing MDR. Stimuli-responsive nanomedicines exhibit many superiorities for reversal of MDR. As smart systems, stimuli-responsive nanomedicines are desirable for achieving site-specific accumulation and triggered drug release in response to slight changes in physicochemical properties in pathological conditions or to exogenous stimuli. In this review, we highlight the current progress of various nanomedicines with different stimuli-responsive capabilities for overcoming MDR. The materials, design, construction as well as efficacy in overcoming MDR of these nanomedicines are discussed. Eventually, we look forward to forthcoming intelligent nanoparticle systems with new mechanisms to deliver drugs for practical applications in conquering cancer MDR. Ivyspring International Publisher 2018-01-01 /pmc/articles/PMC5817110/ /pubmed/29463999 http://dx.doi.org/10.7150/thno.22679 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Zhou, Lei
Wang, Hao
Li, Yaping
Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance
title Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance
title_full Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance
title_fullStr Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance
title_full_unstemmed Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance
title_short Stimuli-Responsive Nanomedicines for Overcoming Cancer Multidrug Resistance
title_sort stimuli-responsive nanomedicines for overcoming cancer multidrug resistance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817110/
https://www.ncbi.nlm.nih.gov/pubmed/29463999
http://dx.doi.org/10.7150/thno.22679
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