Abstract
Diketopyrrolopyrrole (DPP) derivatived photosensitizers (PSs) with near infrared (NIR) absorption and good photophysical properties have drawn tremendous attention in cancer phototherapy. However, current DPP derivatives present unsatisfactory quantum yield of singlet oxygen (1O2) due to the large energy gap between the excited singlet and triplet states. To tackle this challenge, herein the DPP core is functionalized with triphenylphosphine-Au(I) group (ThDPP-Au), leading to a high 1O2 quantum yield of 0.65. Theoretical calculation attributes the enhancement to spin-orbit coupling and population of the triplet excition upon photoexcitation. The hydrophilic ThDPP-Au nanoparticals (NPs) are prepared via nano-reprecipitation, which displays homogeneous size and excellent light absorption ability (ε=4.382×104 M−1 cm−1). And the ThDPP-Au NPs exhibit low dark toxicity and high phototoxicity, which can effectively kill tumor cells via 1O2 induced mitochondrial apoptotic pathway upon irradiation. Furthermore, in vivo experiments demonstrate that ThDPP-Au NPs can selective accumulation in tumor and present excellent synergistic photodynamic/photothermal therapy guided by fluorescence and photothermal dual imaging.
Original language | English |
---|---|
Pages (from-to) | 55-64 |
Number of pages | 10 |
Journal | Science China Chemistry |
Volume | 63 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 1 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019, Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature.
ASJC Scopus Subject Areas
- General Chemistry
Keywords
- diketopyrrolopyrrole-Au(I)
- photodynamic therapy
- photothermal therapy
- singlet oxygen