| Literature DB >> 26881288 |
Sheng Wang1,2,3, Peng Huang1, Xiaoyuan Chen3.
Abstract
Both passive targeting and actively enhanced cellular internalization play significant roles in tumor-targeted therapy. Programmed specific targeting, as a novel targeting strategy that exploits stimuli-responsive structures, expects that nanocarriers show high stability during blood circulation for efficient passive targeting, then respond to tumor internal or external stimuli and transform into more cell-interactive forms upon arrival at the tumor tissue for enhanced cellular internalization. In this Perspective, we introduce recent advances in the design and development of stimuli-responsive programmed specific targeting nanomedicines, which are based on switchable surface charge, activatable targeting molecules, and variable coatings, to combine the advantages of passive targeting and actively enhanced cellular internalization.Entities:
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Year: 2016 PMID: 26881288 PMCID: PMC5223089 DOI: 10.1021/acsnano.6b00870
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881