| Literature DB >> 30387923 |
Lu Yang1, Hao Sun2, Yuan Liu1,3, Weijia Hou1, Yu Yang1,4, Ren Cai3, Cheng Cui1,3, Penghui Zhang1, Xiaoshu Pan1, Xiaowei Li1, Long Li1, Brent S Sumerlin2, Weihong Tan1,3,4.
Abstract
Photoresponsive materials are emerging as ideal carriers for precisely controlled drug delivery owing to their high spatiotemporal selectivity. However, drawbacks such as slow release kinetics, inherent toxicity, and lack of targeting ability hinder their translation into clinical use. We constructed a new DNA aptamer-grafted photoresponsive hyperbranched polymer, which can self-assemble into nanoparticles, thereby achieving biocompatibility and target specificity, as well as light-controllable release behavior. Upon UV-irradiation, rapid release induced by disassembly was observed for Nile Red-loaded nanoparticles. Further in vitro cell studies confirmed this delivery system's specific binding and internalization performance arising from the DNA aptamer corona. The DOX-loaded nanoassembly exhibited selective phototriggered cytotoxicity towards cancer cells, indicating its promising therapeutic effect as a smart drug delivery system.Entities:
Keywords: aptamers; drug delivery; hyperbranched polymers; photoresponsive systems; self-assembly
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Year: 2018 PMID: 30387923 PMCID: PMC6442708 DOI: 10.1002/anie.201809753
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336