| Literature DB >> 29757483 |
Zijian Zhou1, Alexander Chan1, Zhantong Wang1, Xiaolin Huang1, Guocan Yu1, Orit Jacobson1, Sheng Wang1, Yijing Liu1, Lingling Shan1, Yunlu Dai1, Zheyu Shen1, Lisen Lin1, Wei Chen1, Xiaoyuan Chen1.
Abstract
The approach of concurrent-to-synchronous chemoradiation has now been advanced by well-designed nanovesicles that permit X-ray irradiation-triggered instant drug release. The nanovesicles consist of Au nanoparticles tethered with irradiation labile linoleic acid hydroperoxide (LAHP) molecules and oxidation-responsive poly(propylene sulfide)-poly(ethylene glycol) (PPS-PEG) polymers, where DOX were loaded in the inner core of the vesicles (Au-LAHP-vDOX). Upon irradiation, the in situ formation of hydroxyl radicals from LAHP molecules triggers the internal oxidation of PPS from being hydrophobic to hydrophilic, leading to degradation of the vesicles and burst release of cargo drugs. In this manner, synchronous chemoradiation showed impressive anticancer efficacy both in vitro and in a subcutaneous mouse tumor model by one-dose injection and one-time irradiation.Entities:
Keywords: cancer therapy; chemoradiation; drug release; nanovesicles; oxidation responsive
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Year: 2018 PMID: 29757483 PMCID: PMC6251710 DOI: 10.1002/anie.201802351
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336