Donor–Acceptor Modulating of Ionic AIE Photosensitizers for Enhanced ROS Generation and NIR‐II Emission

Author:

Yang Xueqin12ORCID,Wang Xinyuan13,Zhang Xun3,Zhang Jianyu1,Lam Jacky W. Y.1,Sun Haitao45,Yang Jinglei1,Liang Yongye3,Tang Ben Zhong16ORCID

Affiliation:

1. Department of Chemistry Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Department of Mechanical and Aerospace Engineering Division of Life Science State Key Laboratory of Molecular Neuroscience and Department of Chemical and Biological Engineering The Hong Kong University of Science and Technology Clear Water Bay Kowloon Hong Kong

2. Bioscience and Biomedical Engineering Thrust System Hub The Hong Kong University of Science and Technology (Guangzhou) Guangdong 511400 China

3. Department of Materials Science and Engineering Southern University of Science and Technology Guangdong 518055 China

4. State Key Laboratory of Precision Spectroscopy School of Physics and Electronic Science East China Normal University Shanghai 200241 China

5. Collaborative Innovation Center of Extreme Optics Shanxi University Taiyuan Shanxi 030006 China

6. School of Science and Engineering Shenzhen Institute of Aggregate Science and Technology The Chinese University of Hong Kong Shenzhen (CUHK‐Shenzhen) Guangdong 518172 China

Abstract

AbstractPhotosensitizers (PSs) with aggregation‐induced emission (AIE) characteristics are competitive candidates for bioimaging and therapeutic applications. However, their short emission wavelength and nonspecific organelle targeting hinder their therapeutic effectiveness. Herein, a donor–acceptor modulation approach is reported to construct a series of ionic AIE photosensitizers with enhanced photodynamic therapy (PDT) outcomes and fluorescent emission in the second near‐infrared (NIR‐II) window. By employing dithieno[3,2‐b:2′,3′‐d]pyrrole (DTP) and indolium (In) as the strong donor and acceptor, respectively, the compound DTP‐In exhibits a substantial redshift in absorption and fluorescent emission reach to NIR‐II region. The reduced energy gap between singlet and triplet states in DTP‐In also increases the reactive oxygen species (ROS) generation rate. Further, DTP‐In can self‐assemble in aqueous solutions, forming positively charged nanoaggregates, which are superior to conventional encapsulated nanoparticles in cellular uptake and mitochondrial targeting. Consequently, DTP‐In aggregates show efficient photodynamic ablation of 4T1 cancer cells and outstanding tumor theranostic in vivo under 660 nm laser irradiation. This work highlights the potential of molecular engineering of donor–acceptor AIE PSs with multiple functionalities, thereby facilitating the development of more effective strategies for cancer therapy.

Funder

Innovation and Technology Commission

Publisher

Wiley

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