Programmable Chemotherapy and Immunotherapy against Breast Cancer Guided by Multiplexed Fluorescence Imaging in the Second Near-Infrared Window.
Xiaoxia HaoChunyan LiYejun ZhangHaozhi WangGuangcun ChenMao WangQiangbin WangPublished in: Advanced materials (Deerfield Beach, Fla.) (2018)
Combined chemotherapy and immunotherapy have demonstrated great potential in cancer treatment. However, it is difficult to provide clear information of the pharmacokinetics and pharmacodynamics of chemodrugs and transplanted immune cells in vivo by traditional approaches, resulting in inadequate therapy. Here, a multiplexed intravital imaging strategy by using fluorescence in the second near-infrared window (NIR-II) is first developed to visualize the two events of chemotherapy and immunotherapy in vivo, so that a combinational administration is programed to improve the therapeutical effects against a mouse model of human breast cancer. In detail, Ag2 Se quantum dots (QDs) (λEm = 1350 nm) loaded with stromal-cell-derived factor-1α (SDF-1α) and chemodrug doxorubicin (DOX) are first administrated to deliver the SDF-1α and DOX to the tumor site. After their arrival, monitored by Ag2 Se QD fluorescence, natural killer (NK)-92 cells labeled with Ag2 S QDs (λEm = 1050 nm) are intravenously injected so that the cells are recruited to the tumor by the chemotaxis of SDF-1α, which is visualized by Ag2 S QD fluorescence. Such an imaging approach allows simultaneous evaluation of the behaviors of individual injections in vivo, and facilitates optimized administration regimens, resulting in enhanced tumor inhibition.
Keyphrases
- quantum dots
- fluorescence imaging
- photodynamic therapy
- energy transfer
- nk cells
- mouse model
- single molecule
- locally advanced
- high resolution
- drug delivery
- sensitive detection
- highly efficient
- induced apoptosis
- single cell
- visible light
- bone marrow
- cancer therapy
- endothelial cells
- stem cells
- risk assessment
- squamous cell carcinoma
- radiation therapy
- mass spectrometry
- computed tomography
- ultrasound guided
- cell proliferation
- induced pluripotent stem cells
- drug release
- pluripotent stem cells
- wound healing
- human health
- breast cancer risk