4.6 Article

A glutathione-activatable photodynamic and fluorescent imaging monochromatic photosensitizer

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 5, Issue 22, Pages 4239-4245

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7tb00724h

Keywords

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Funding

  1. National Natural Science Foundation of China [21504089, 51373167, 51522307]
  2. Program for Science and Technology Innovation Talents in Universities of Henan Province [15HASTIT002]
  3. Natural Science Foundation of Xuchang University [2017ZD007]
  4. Science and Technology of Henan Province [162300410209]

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The currently available photodynamic sensitizers usually lead to undesirable side effects, including dark toxicity from heavy-atom effect and nonspecific phototoxicity. To address these issues, we designed and prepared a smart photosensitizer from boron dipyrromethene (BODIPY), and the dark toxicity and phototoxicity were reduced via heavy-atom-free substitution and controllable photosensitization, respectively. Importantly, the photodynamic effect together with fluorescence imaging can be simultaneously switched on through the suppression of intramolecular charge transfer (ICT) and photoinduced electron-transfer (PeT) induced by cancer-related biothiol glutathione (GSH) in a buffer solution. Moreover, the sensitizer exhibits obvious fluorescence enhancement and selective phototoxicity towards cancer cells in a biological system upon irradiation. The present monochromatic photosensitizer, which combines fluorescence imaging and targeted PDT treatment within a single chromophore, possesses great potentials as a new activatable theranostic reagent in cancer therapy.

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