Spatiotemporally controlled O2 and singlet oxygen self-sufficient nanophotosensitizers enable the in vivo high-yield synthesis of drugs and efficient hypoxic tumor therapy. Issue 33 (11th August 2020)

• Record Type: Journal Article
• Authors: He, Suisui; Lu, Siyu; Liu, Sha; Li, Tianrong; Li, Jieling; Sun, Shihao; Liu, Meilin; Liang, Kun; Fu, Xu; Chen, Fengjuan; Meng, Genping; Zhang, Lang; Hai, Jun; Wang, Baodui
• Is Part Of: Chemical science. Volume 11:Issue 33(2020)
• Page Start: 8817
• Page End: 8827
• Publication Date: 2020-08-11
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc02387f
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : A porous photosensitizer displaying catalase-like activity and drug synthesis ability was synthesized for the synergistic chemo-photodynamic therapy, opening new promising ways for carrying out the precise cooperative treatment of hypoxic tumors. Abstract : Carrying out the in vivo syntheses of drugs toxic to tumors based on the specific features of the tumor microenvironment is critical for ensuring specific antitumor efficacy. However, achieving in situ high-yield synthetic toxic drugs from non-toxic agents and reducing their drug resistance in hypoxic tumors remain challenges. Herein we created a tumor-microenvironment-responsive porous Pt/Pt(iv ) methylene blue coordination polymer nanoshuttle (Pt/PtMBCPNS) photosensitizer with spatiotemporally controlled O2 and singlet oxygen ( 1 O2 ) self-sufficient for the in vivo high-yield synthesis of drugs and efficient hypoxic tumor therapy. After being endocytosed, the nanophotosensitizer as a cascade catalyst was observed to effectively catalyze the conversion of endogenous H2 O2 to O2, and was hence found to play a dual role in the enhanced tumor therapy. PtMBCPNSs, upon being irradiated with red light, efficiently converted O2 into 1 O2 . Subsequently, 1 O2 oxidized non-toxic 1, 5-dihydroxynaphthalene to form the anticancer agent juglone with a high yield. In addition, O2 was found to be able to improve the hypoxic microenvironment without light irradiation, thus enhancing the antitumor efficacy of the produced drugs and reducing drug resistance. As a result, by enhancing the synergistic effect of the treatment, this nanophotosensitizer significantly inhibited the growth of tumors and avoided damage to normal tissues/organs. Collectively, this work highlights a robust nanoplatform with the spatiotemporally controlled in vivo high-yield synthesis of drugs and generation of O2 to help overcome the current limitations of chemical-based therapies against hypoxic tumors.