菁
光敏剂
光热治疗
光动力疗法
光漂白
光化学
系统间交叉
化学
合理设计
偶氮苯
聚集诱导发射
生物物理学
酞菁
材料科学
光毒性
吲哚青绿
组合化学
共轭体系
光降解
动力学
癌症研究
癌细胞
光电子学
作者
Xiang Sun,Di Li,Yuqin Chen,Huanren Cheng,Ruping Huang,Juan Jin,Wentao Yang,Bin Huang,Ning Gu
标识
DOI:10.1016/j.bioactmat.2026.01.048
摘要
Photothermal and photodynamic therapies (PTT/PDT) have emerged as promising noninvasive tumor treatments. Effective regulation of excited-state properties in near-infrared (NIR) photosensitizers (PSs) is crucial for enhancing therapeutic efficacy by minimizing photobleaching and optimizing energy dissipation pathways. Rational molecular design of NIR PSs to simultaneously improve photostability and favor non-radiative decay mechanism holds significant potential for revolutionizing tumor treatment. In this work, a series of NIR photosensitizer isomers ( o 2CyO-AB and p 2CyO-AB) were designed and synthesized by combining azobenzene group and a cyanine dye (Cy-Cl). Compared with Cy-Cl, both isomers exhibited significantly improved photostability and non-radiative transitions. For the first time, single-crystal structural analysis revealed that azobenzene incorporation shortened the conjugated double-bond system in the cyanine dye, leading to a dramatic enhancement in photostability. Different substitution positions exerted a significant influence on the non-radiative transition process. Notably, the non-radiative transition of o 2CyO-AB was dominated by intersystem crossing with a remarkable 15-fold increase in the yield of 1 O 2 compared with the clinical NIR PS Indocyanine green, while the non-radiative decay of p 2CyO-AB mainly proceeded via thermal deactivation with a high photothermal conversion efficiency of 51.02%. In a proof-of-concept study using oral squamous cell carcinoma HN6 as a model, o 2CyO-AB mediated potent combined PTT/PDT effects, achieving a high tumor growth inhibition rate of 95.41% in vivo within 14 days. Therefore, modifying PSs with azobenzene groups holds promise for enhancing their phototherapeutic performance, offering new strategies and approaches for developing efficient and precise tumor PSs. • A series of NIR isomers with simultaneously enhanced photostability and non-radiative transitions were synthesized. • Azobenzene incorporation shortened the conjugated double-bond system in the PSs, leading to enhanced photostability. • o 2CyO-AB mediated potent combined PTT/PDT effects, achieving a high tumor growth inhibition rate of 95.41% in vivo .
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