Ternary Heteronanocrystals with Dual-Heterojunction for Boosting Near-Infrared-Triggered Photo-Chemodynamic Therapy
Yufang Kou, Minchao Liu, Mengmeng Hou, Tiancong Zhao, Liang Chen, Jia Jia, Yating Zhan, Kui Yan, Boya Wang, Fan Zhang, Dongyuan Zhao, Xiaomin Li
Abstract
Strongly coupled interfaces in the epitaxial growth heteronanocrystals (HNCs) provide advanced functionalities regarding interface connection, electron transfer, and carrier separation. However, the majority of current nanocomposites primarily focus on a single heterojunction involving only two subunits, which hinders the achievement of optimized synergy energy transfer among more than two components. Herein, ternary NaGdF 4:Yb,Tm-TiO 2:F-Fe 3 O 4 HNCs with dual-heterojunction were synthesized based on the crystal plane epitaxial growth strategy for boosting near-infrared (NIR)-triggered photo-chemodynamic therapy (PCDT). Fluorine is doped into TiO 2 (TiO 2:F), which not only enhances the exposure of the (001) facet of TiO 2 for Fe 3 O 4 subunit growth but also promotes the growth of the NaGdF 4:Yb,Tm upconversion nanocrystal (UCNC) subunit, enabling an epitaxial combination of all three components. Upon NIR irradiation, the UCNC subunit transfers the light energy of the absorbed NIR light to the TiO 2:F subunit, thereby facilitating the generation of electron–hole pairs within TiO 2:F. Due to different work functions between TiO 2:F and Fe 3 O 4 in the ternary HNCs, electrons tend to transfer from TiO 2:F into Fe 3 O 4, resulting in a reduction of inactive Fe 3+ into active Fe 2+ and further enhancing the Fenton-catalysis performance. Simultaneously, the efficient separation of electrons and holes improves the photocatalytic oxidation property induced by TiO 2:F. Based on ternary UCNC-TiO 2:F-Fe 3 O 4 HNCs boosting Fenton catalysis and photocatalysis at the single particle level, as a proof of concept, we propose a NIR light-triggered PCDT (NIR-PCDT) synergistically enhanced tumor treatment strategy. In vitro and in vivo experiments demonstrate that this NIR-PCDT agent exhibits a pronounced ability to generate reactive oxygen species, effectively inducing apoptosis in tumor cells.