Upconversion NIR-II fluorophores for mitochondria-targeted cancer imaging and photothermal therapy.
Hui ZhouXiaodong ZengAnguo LiWenyi ZhouLin TangWenbo HuQu-Li FanXianli MengHai DengLian DuanYanqin LiZixin DengXuechuan HongYuling XiaoPublished in: Nature communications (2020)
NIR-II fluorophores have shown great promise for biomedical applications with superior in vivo optical properties. To date, few small-molecule NIR-II fluorophores have been discovered with donor-acceptor-donor (D-A-D) or symmetrical structures, and upconversion-mitochondria-targeted NIR-II dyes have not been reported. Herein, we report development of D-A type thiopyrylium-based NIR-II fluorophores with frequency upconversion luminescence (FUCL) at ~580 nm upon excitation at ~850 nm. H4-PEG-PT can not only quickly and effectively image mitochondria in live or fixed osteosarcoma cells with subcellular resolution at 1 nM, but also efficiently convert optical energy into heat, achieving mitochondria-targeted photothermal cancer therapy without ROS effects. H4-PEG-PT has been further evaluated in vivo and exhibited strong tumor uptake, specific NIR-II signals with high spatial and temporal resolution, and remarkable NIR-II image-guided photothermal therapy. This report presents the first D-A type thiopyrylium NIR-II theranostics for synchronous upconversion-mitochondria-targeted cell imaging, in vivo NIR-II osteosarcoma imaging and excellent photothermal efficiency.
Keyphrases
- photodynamic therapy
- cancer therapy
- fluorescence imaging
- drug release
- drug delivery
- high resolution
- small molecule
- cell death
- fluorescent probe
- reactive oxygen species
- mass spectrometry
- endoplasmic reticulum
- stem cells
- squamous cell carcinoma
- dna damage
- cell proliferation
- single cell
- machine learning
- young adults
- big data
- signaling pathway
- heat stress
- endoplasmic reticulum stress