光敏剂
木筏
聚合
化学
糖类聚合物
催化作用
光动力疗法
高分子化学
光化学
有机化学
聚合物
作者
Jiaoyang Zhu,Jiahui Lin,Ruili Wang,Zhiyuan Ma,Weiwei Zuo,Meifang Zhu
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2025-03-24
卷期号:26 (4): 2654-2664
被引量:4
标识
DOI:10.1021/acs.biomac.5c00090
摘要
PET-RAFT polymerization enables precise polymer synthesis, yet conventional systems require an excess chain transfer agent (CTA) over unbound photocatalysts (PCs). Herein, a self-catalyzed strategy employing polymerizable porphyrin MTPPZnH as a dual-functional PC effectively embeds high photosensitizer content into glycopolymers for photodynamic therapy (PDT). Three galactose-bearing monomers (acrylate, methacrylate, 4-vinylbenzoate) were polymerized via PET-RAFT under optimized light conditions, achieving satisfactory Mn and relatively narrow Đ. Mechanistic studies revealed that photoexcited MTPPZnH transfers electrons/energy to CTA via a PET process, initiating polymerization, with DMSO enhancing oxygen depletion. Water-soluble glycopolymeric photosensitizers exhibited high fluorescence and singlet oxygen quantum yield. In vitro, galactose-bearing photosensitizers showed superior ASGPR-mediated endocytosis in HepG2 cells over Huh-7 and MCF-7 cells, enabling targeted PDT. The incorporation of MTPPZnH contributes to an effective multifunctional strategy, offering a promising approach for the development of high photosensitizer-embedded polymeric photosensitizers for potential PDT applications.
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