Tuning Organelle Specificity and Photodynamic Therapy Efficiency by Molecular Function Design

• Published in: ACS nano Vol. 13; no. 10; pp. 11283 - 11293
• Main Authors: Liu, Zhiyang, Zou, Hang, Zhao, Zheng, Zhang, Pengfei, Shan, Guo-Gang, Kwok, Ryan T. K, Lam, Jacky W. Y, Zheng, Lei, Tang, Ben Zhong
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 22.10.2019
• Subjects: aggregation-induced emission; cationization; photodynamic therapy; organelle-specific imaging; reactive oxygen species
• ISSN: 1936-0851; 1936-086X; 1936-086X
• DOI: 10.1021/acsnano.9b04430

Efficient organic photosensitizers (PSs) have attracted much attention because of their promising applications in photodynamic therapy (PDT). However, guidelines on their molecular design are rarely reported. In this work, a series of PSs are designed and synthesized based on a triphenylamine-azafluorenone core. Their structure–property-application relationships are systematically studied. Cationization is an effective strategy to enhance the PDT efficiency of PSs by targeting mitochondria. From the molecularly dispersed state to the aggregate state, the fluorescence and the reactive oxygen species generation efficiency of PSs with aggregation-induced emission (AIE) increase due to the restriction of the intramolecular motions and enhancement of intersystem crossing. Cationized mitochondrion-targeting PSs show higher PDT efficiency than that of nonionized ones targeting lipid droplets. The ability of AIE PSs to kill cancer cells can be further enhanced by combination of PDT with radiotherapy. Such results should trigger research enthusiasm for designing and synthesizing AIE PSs with better PDT efficiency and properties.