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Updated: Jan 15, 2026

Method of Direct Segmental Intra-hepatic Delivery Using a Rat Liver Hilar Clamp Model
Published on: April 2, 2017
Side-Chain Sulfonation to Modulate Hydroxyl Radical Generators for Efficient Suppression of Hepatoma Cells under
Shouchi Ji1, Junjun Wang2, Lixin Ma1
1School of Chemistry and Chemical Engineering, Key Laboratory of Structure and Functional Regulation of Hybrid Materials Ministry of Education, Key Laboratory of Functional Inorganic Materials Chemistry of Anhui Province, and Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials of Anhui Province, Anhui University, Hefei 230601, P. R. China.
Abstract:
The development of type I photosensitizer (PS) targeting subcellular organelles that directly destroy key subcellular compartments and overcome the hypoxic environment has become a critical breakthrough for improving therapeutic effects on tumors. Herein, we proposed a simple tactic of side-chain sulfonation to construct the subcellular organelles targeting type I PS. Initially, the traditional lipophilic donor-π-acceptor (D-π-A) system (3SSYDI) was constructed, which exhibited type II reactive oxygen species generation capability and lipid droplets (LDs)-targeting property. Innovatively, the heavy-atom-free sulfonate ion was introduced to achieve side-chain sulfonation. The modulated 3SSYDS not only exhibited optimal biosafety but also possessed lower impedance and higher photocurrent intensity, which facilitated superior electron transfer to generate superoxide anions (O2-•). Notably, in biological aqueous systems, O2-• combined with protons to further produce hydrogen peroxide, thereby triggering the Haber-Weiss reaction to produce the most reactive hydroxyl radical (•OH), achieving more effective suppression of cancer cells even under hypoxic conditions. This study presents a simple strategy of side-chain sulfonation that activated highly toxic •OH generation in traditional D-π-A systems, providing an efficient solution for treating hypoxic tumors.
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