铱
材料科学
单线态氧
激发态
光化学
化学
氧气
催化作用
有机化学
原子物理学
物理
作者
Gan Lin,Geoffrey T. Nash,Taokun Luo,Indranil Ghosh,Siddhartha Sohoni,Andrew J. Christofferson,Gang Liu,Gregory S. Engel,Wenbin Lin
标识
DOI:10.1002/adma.202212069
摘要
Abstract Although sonodynamic therapy (SDT) has shown promise for cancer treatment, the lack of efficient sonosensitizers (SSs) has limited the clinical application of SDT. Here, a new strategy is reported for designing efficient nano‐sonosensitizers based on 2D nanoscale metal–organic layers (MOLs). Composed of Hf‐oxo secondary building units (SBUs) and iridium‐based linkers, the MOL is anchored with 5,10,15,20‐tetra( p ‐benzoato)porphyrin (TBP) sensitizers on the SBUs to afford TBP@MOL. TBP@MOL shows 14.1‐ and 7.4‐fold higher singlet oxygen ( 1 O 2 ) generation than free TBP ligands and Hf‐TBP, a 3D nanoscale metal–organic framework, respectively. The 1 O 2 generation of TBP@MOL is enhanced by isolating TBP SSs on the SBUs of the MOL, which prevents aggregation‐induced quenching of the excited sensitizers, and by triplet–triplet Dexter energy transfer between excited iridium‐based linkers and TBP SSs, which more efficiently harnesses broad‐spectrum sonoluminescence. Anchoring TBP on the MOL surface also enhances the energy transfer between the excited sensitizer and ground‐state triplet oxygen to increase 1 O 2 generation efficacy. In mouse models of colorectal and breast cancer, TBP@MOL demonstrates significantly higher SDT efficacy than Hf‐TBP and TBP. This work uncovers a new strategy to design effective nano‐sonosensitizers by facilitating energy transfer to efficiently capture broad‐spectrum sonoluminescence and enhance 1 O 2 generation.
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