Chemical Research in Chinese Universities ›› 2026, Vol. 42 ›› Issue (2): 400-411.doi: 10.1007/s40242-026-5315-x

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Polymer-based Phototherapeutic Nanoagents for Multimodal Image-guided Cancer Therapy

WANG Zhixiong1,2, ZHANG Zhenhui1,2   

  1. 1. MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, School of Optoelectronic Science and Engineering, South China Normal University, Guangzhou 510631, P. R. China;
    2. Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, School of Optoelectronic Science and Engineering, South China Normal University, Guangzhou 510631, P. R. China
  • Received:2025-12-31 Online:2026-04-01 Published:2026-04-02
  • Contact: WANG Zhixiong,E-mail:wangzhixiong@m.scnu.edu.cn;ZHANG Zhenhui,E-mail:zzh@scnu.edu.cn E-mail:wangzhixiong@m.scnu.edu.cn;zzh@scnu.edu.cn
  • Supported by:
    This work was supported by the China Postdoctoral Science Foundation(No. 2024M750971).

Abstract: Polymer-based phototherapeutic nanoagents provide an effective route to integrate fluorescence (FL) and photoacoustic (PA) imaging with photothermal therapy (PTT) and photodynamic therapy (PDT). This review highlights covalently engineered polymer-chromophore systems, in which photothermal agents or photosensitizers are incorporated into polymer backbones via robust linkages (e.g., amide/ester and related bonds) or through polymerizable chromophore monomers. Tumor microenvironment-responsive motifs (e.g., disulfide and thioketal units) further enable activatable behavior and improved selectivity. Importantly, amphiphilic conjugates self-assemble into nanodots, polymersomes, and nanofibers, and assembly morphology and chromophore packing can reprogram excited-state pathways, thereby tuning FL/PA outputs, photothermal conversion, and Type I/II ROS generation. We discuss representative porphyrin/phthalocyanine, heptamethine cyanine, Changsha Red (xanthene-derived), and Nile Blue platforms for multimodal image-guided cancer phototherapy, including mechanism-integrated strategies, such as microenvironment activation, organelle targeting, and immunomodulation. Finally, we outline key challenges and opportunities for translation, including quantitative structure-property correlations, scalable morphology control, standardized photophysical reporting, and biosafety evaluation.

Key words: Polymer-chromophore conjugate, Phototherapeutic nanoagent, Photoacoustic imaging, Fluorescence imaging, Photodynamic and photothermal therapy