Literature DB >> 27569390

Smart nanoparticles improve therapy for drug-resistant tumors by overcoming pathophysiological barriers.

Jian-Ping Liu1,2, Ting-Ting Wang2, Dang-Ge Wang2, An-Jie Dong1, Ya-Ping Li2, Hai-Jun Yu2.   

Abstract

The therapeutic outcome of chemotherapy is severely limited by intrinsic or acquired drug resistance, the most common causes of chemotherapy failure. In the past few decades, advancements in nanotechnology have provided alternative strategies for combating tumor drug resistance. Drug-loaded nanoparticles (NPs) have several advantages over the free drug forms, including reduced cytotoxicity, prolonged circulation in the blood and increased accumulation in tumors. Currently, however, nanoparticulate drugs have only marginally improved the overall survival rate in clinical trials because of the various pathophysiological barriers that exist in the tumor microenvironment, such as intratumoral distribution, penetration and intracellular trafficking, etc. Smart NPs with stimulus-adaptable physico-chemical properties have been extensively developed to improve the therapeutic efficacy of nanomedicine. In this review, we summarize the recent advances of employing smart NPs to treat the drug-resistant tumors by overcoming the pathophysiological barriers in the tumor microenvironment.

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Year:  2016        PMID: 27569390      PMCID: PMC5220546          DOI: 10.1038/aps.2016.84

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  67 in total

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  8 in total

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