4.8 Article

Imaging-Guided Combined Photothermal and Radiotherapy to Treat Subcutaneous and Metastatic Tumors Using Iodine-131-Doped Copper Sulfide Nanoparticles

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 25, Issue 29, Pages 4689-4699

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201502003

Keywords

cancer metastasis; copper sulfide; multimodal imaging; photothermal therapy; radiotherapy

Funding

  1. National Basic Research Program of China (973 Program) [2014CB931900, 2012CB932600]
  2. National Natural Science Foundation of China [81471716, 81302383, 31400861, 21207164, 51222203]
  3. National Natural Science Foundation of Jiangsu Province [BK20140320, BK20130005]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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Combining different therapeutic strategies to treat cancer by overcoming limitations of conventional cancer therapies has shown great promise in both fundamental and clinical studies. Herein, by adding I-131 when making iodine-doped CuS nanoparticles, CuS/[I-131]I nanoparticles are obtained, which after functionalization with polyethylene glycol (PEG) are used for radiotherapy (RT) and photothermal therapy (PTT), by utilizing their intrinsic high near-infrared absorbance and the doped I-131-radioactivity, respectively. The combined RT and PTT based on CuS/[I-131]I-PEG is then conducted, achieving remarkable synergistic therapeutic effects as demonstrated in the treatment of subcutaneous tumors. In the meanwhile, as revealed by bimodal nuclear imaging and computed tomography (CT) imaging, it is found that CuS/[I-131]I-PEG nanoparticles after being injected into primary solid tumors could migrate to and retain in their nearby sentinel lymph nodes. Importantly, the combined RT and PTT applied on those lymph nodes to assist surgical resection of primary tumors results in remarkably inhibited cancer metastasis and greatly prolonged animal survival. In vivo toxicology studies further reveal that our CuS/I-PEG is not obviously toxic to animals at fourfold of the treatment dose. This work thus demonstrates the potential of combining RT and PTT using a single nanoagent for imaging-guided treatment of metastatic tumors.

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