菁
光热治疗
化学
光动力疗法
生物医学中的光声成像
生物物理学
四苯乙烯
离域电子
合理设计
纳米技术
癌细胞
纳米颗粒
聚集诱导发射
纳米医学
吸收(声学)
量子点
光化学
量子产额
癌症
J-骨料
DNA损伤
树枝状大分子
限制
光生物学
电穿孔
作者
Mengyuan Cui,Wenqing Li,Yanli Chen,Huijia Liu,Li Liu,Min Ji,Peng Wang
摘要
ABSTRACT Current phototherapeutic agents based on heptamethine cyanine dyes often rely on symmetric structures, limiting their photodynamic therapy (PDT) efficiency. Herein, we report a novel asymmetric heptamethine cyanine dye (Cyp‐TPE) that features a twisted tetraphenylethylene moiety. This design facilitates the formation of stable aggregate nanoparticles (NPs) with a cross‐arranged structure, as revealed by molecular dynamics simulations. This specific aggregation mode promotes exciton delocalization and dramatically enhances spin‐orbit coupling, leading to an unprecedented ROS quantum yield of 154.54%. Under 808 nm laser irradiation, the Cyp‐TPE NPs demonstrate potent synergistic photodynamic and photothermal activity, concurrently triggering ferroptosis and lysosomal dysfunction, thereby achieving multimodal death of cancer cells. Furthermore, the excellent NIR absorption and photothermal conversion of these aggregates enable precise photothermal imaging (PTI) and photoacoustic imaging (PAI). This work highlights the potential of asymmetric molecular design to overcome the limitations of conventional photosensitizers, offering a robust nanoplatform for imaging‐guided cancer therapy.
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