| Literature DB >> 29141151 |
Yangyun Wang1, Yibin Deng1, Huanhuan Luo1, Aijun Zhu1, Hengte Ke1, Hong Yang1, Huabing Chen1.
Abstract
Stimuli-responsive nanostructures have shown great promise for intracellular delivery of anticancer compounds. A critical challenge remains in the exploration of stimuli-responsive nanoparticles for fast cytoplasmic delivery. Herein, near-infrared (NIR) light-responsive nanoparticles were rationally designed to generate highly efficient cytoplasmic delivery of anticancer agents for synergistic thermo-chemotherapy. The drug-loaded polymeric nanoparticles of selenium-inserted copolymer (I/D-Se-NPs) were rapidly dissociated in several minutes through reactive oxygen species (ROS)-mediated selenium oxidation upon NIR light exposure, and this irreversible dissociation of I/D-Se-NPs upon such a short irradiation promoted continuous drug release. Moreover, I/D-Se-NPs facilitated cytoplasmic drug translocation through ROS-triggered lysosomal disruption and thus resulted in highly preferable distribution to the nucleus even in 5 min postirradiation, which was further integrated with light-triggered hyperthermia for achieving synergistic tumor ablation without tumor regrowth.Entities:
Keywords: cytoplasmic delivery; light-responsive nanoparticles; micelles; photothermal therapy; synergistic therapy
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Year: 2017 PMID: 29141151 DOI: 10.1021/acsnano.7b05214
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881