| Literature DB >> 30265899 |
Kai Zhang1, Yuedong Zhang2, Xiangdan Meng2, Huiting Lu2, Huan Chang2, Haifeng Dong3, Xueji Zhang4.
Abstract
Hypoxia tumor microenvironment is a major challenge for photodynamical therapy (PDT), and hypoxia-activated chemotherapy combined PDT could be promising for enhanced anticancer therapy. In this study, we report an innovative 2-nitroimidazole derivative conjugated polyethylene glycol (PEG) amphoteric polymer theranostic liposome encapsulated a photosensitizer Chlorin e6 (Ce6), hypoxia-activated prodrug Tirapazamine (TPZ) and gene probe for synergistic photodynamic-chemotherapy. Ce6-mediated PDT upon irradiation with a laser induces hypoxia, which leads to the disassembly of the liposome and activates the antitumor activity of TPZ for improved cancer cell-killing. The released co-delivered gene probe could effectively detect the oncogenic intracellular biomarker for diagnosis. Both in vitro and in vivo studies demonstrated the greatly improved anti-cancer activity compared to conventional PDT. This work contributes to the design of hypoxia-responsive multifunctional liposome for tumor diagnosis and hypoxia-activated chemotherapy combined PDT for synergetic therapy, which holds great promise for future cancer therapy.Entities:
Keywords: Drug delivery; Hypoxia activated prodrug; Liposomes; Photodynamic therapy; Tumor hypoxia
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Year: 2018 PMID: 30265899 DOI: 10.1016/j.biomaterials.2018.09.033
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479