| Literature DB >> 31808983 |
Zhiyong Liu1, Tianye Cao2,3, Yudong Xue1, Mengting Li2, Mengsi Wu1, Jonathan W Engle2, Qianjun He3, Weibo Cai2, Minbo Lan1, Weian Zhang1.
Abstract
Nanocarriers are employed to deliver photosensitizers for photodynamic therapy (PDT) through the enhanced penetration and retention effect, but disadvantages including the premature leakage and non-selective release of photosensitizers still exist. Herein, we report a 1 O2 -responsive block copolymer (POEGMA-b-P(MAA-co-VSPpaMA) to enhance PDT via the controllable release of photosensitizers. Once nanoparticles formed by the block copolymer have accumulated in a tumor and have been taken up by cancer cells, pyropheophorbide a (Ppa) could be controllably released by singlet oxygen (1 O2 ) generated by light irradiation, enhancing the photosensitization. This was demonstrated by confocal laser scanning microscopy and in vivo fluorescence imaging. The 1 O2 -responsiveness of POEGMA-b-P(MAA-co-VSPpaMA) block copolymer enabled the realization of self-amplified photodynamic therapy by the regulation of Ppa release using NIR illumination. This may provide a new insight into the design of precise PDT.Entities:
Keywords: block copolymer; drug delivery; photodynamic therapy; reactive oxygen species; self-amplification
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Year: 2020 PMID: 31808983 PMCID: PMC7028480 DOI: 10.1002/anie.201914434
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336