4.8 Article

Biodegradable Calcium Phosphate Nanotheranostics with Tumor-Specific Activatable Cascade Catalytic Reactions-Augmented Photodynamic Therapy

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 14, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202009848

关键词

biomineralization; calcium phosphate nanotheranostics; glucose oxidase; oxygen self-supplying; photodynamic therapy

资金

  1. National Natural Science Foundation of China [21807074, 51802202, 31900945]
  2. National Key R&D Program of China [2018YFA0704000]
  3. Shenzhen Science and Technology Program [KQTD20190929172538530]
  4. Guangdong Province Natural Science Foundation of Ph.D. Start-up Fund [2018A030310574, 2018A030310566]
  5. Guangdong Province Natural Science Foundation of Major Basic Research and Cultivation Project [2018B030308003]
  6. Basic Research Program of Shenzhen [JCYJ20180507182413022, JCYJ20170412111100742]
  7. Fundamental Research Funds for the Central Universities [2020CDJQY-A060]

向作者/读者索取更多资源

This study presents a novel nanoplatform GMCD for tumor microenvironment-specific activatable cascade catalytic reactions-augmented PDT, which can effectively accumulate at tumor sites, promote GOx catalytic reaction, alleviate tumor hypoxia, enhance production of cytotoxic singlet oxygen, and amplify oxidative damage of cancer cells. GMCD demonstrates superior therapeutic effects on 4T1-tumor bearing mice through a long-term cascade catalytic reactions-augmented PDT.
Photodynamic therapy (PDT) is exploited as a promising strategy for cancer treatment. However, the hypoxic solid tumor and the lack of tumor-specific photosensitizer administration hinder the further application of oxygen (O-2)-dependent PDT. In this study, a biodegradable and O-2 self-supplying nanoplatform for tumor microenvironment (TME)-specific activatable cascade catalytic reactions-augmented PDT is reported. The nanoplatform (named GMCD) is constructed by coloading catalase (CAT) and sinoporphyrin sodium (DVDMS) in the manganese (Mn)-doped calcium phosphate mineralized glucose oxidase (GOx) nanoparticles. The GMCD can effectively accumulate in tumor sites to achieve an off to on fluorescence transduction and a TME-activatable magnetic resonance imaging. After internalization into cancer cells, the endogenous hydrogen peroxide (H2O2) can be catalyzed to generate O-2 by CAT, which not only promotes GOx catalytic reaction to consume more intratumoral glucose, but also alleviates tumor hypoxia and enhances the production of cytotoxic singlet oxygen from light-triggered DVDMS. Moreover, the H2O2 generated by GOx-catalysis can be converted into highly toxic hydroxyl radicals by Mn2+-mediated Fenton-like reaction, further amplifying the oxidative damage of cancer cells. As a result, GMCD displays superior therapeutic effects on 4T1-tumor bearing mice by a long term cascade catalytic reactions augmented PDT.

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