Redox-active polyphenol nanoparticles deprive endogenous glutathione of electrons for ROS generation and tumor chemodynamic therapy

被引:5
|
作者
Wang, Yifei [1 ]
Wang, Jia [4 ,5 ,6 ]
Jiao, Yunke [1 ]
Chen, Kangli [1 ]
Chen, Tianhao [1 ]
Wu, Xinping [4 ,5 ,6 ]
Jiang, Xingwu [2 ,3 ]
Bu, Wenbo [2 ,3 ]
Liu, Changsheng [1 ]
Qu, Xue [1 ,7 ,8 ]
机构
[1] East China Univ Sci & Technol, Frontiers Sci Ctr Materiobiol & Dynam Chem, Sch Mat Sci & Engn, Key Lab Ultrafine Mat,Minist Educ, Shanghai 200237, Peoples R China
[2] Fudan Univ, Dept Mat Sci, Shanghai 200433, Peoples R China
[3] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[4] East China Univ Sci & Technol, Sch Chem & Mol Engn, State Key Lab Green Chem Engn & Ind Catalysis, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
[5] East China Univ Sci & Technol, Sch Chem & Mol Engn, Frontiers Sci Ctr Materiobiol & Dynam Chem, Feringa Nobel Prize Scientist Joint Res Ctr,Ctr Co, 130 Meilong Rd, Shanghai 200237, Peoples R China
[6] East China Univ Sci & Technol, Res Inst Ind Catalysis, Sch Chem & Mol Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
[7] Shanghai Univ, Wenzhou Inst, Wenzhou 325000, Peoples R China
[8] Shanghai Frontier Sci Ctr Optogenet Tech Cell Meta, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyphenol-based CDT nanomaterial; Redox activity; Electron transporting; NOX enzyme-like ROS generator; GSH function reverse; QUINONES; PRODRUG; CELLS; XPS;
D O I
10.1016/j.actbio.2023.09.037
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chemodynamic therapy (CDT) based on generating reactive oxygen species (ROS) is promising for cancer treatment. However, the intrinsic H2O2 is deficient for CDT, and glutathione (GSH) eliminates ROS to pro-tect tumor cells from ROS cytotoxicity. Herein, we propose a strategy to switch the electron flow direction of GSH for O 2 reduction and ROS generation rather than ROS clearance by using P(DA-Fc) nanoparticles, which are polymerized from ferrocenecarboxylic acid (Fc) coupled dopamine. P(DA-Fc) NPs with phenol-quinone conversion ability mimic NOX enzyme to deprive electrons from GSH to reduce O 2 for H2O2 generation; the following center dot OH release can be triggered by Fc. Semiquinone radicals in P(DA-Fc) are significantly enhanced after GSH treatment, further demonstrated with strong single-electron reduction ability by calculation. In vitro and in vivo experiments indicate that P(DA-Fc) can consume intrinsic GSH to pro-duce endogenous ROS; ROS generation strongly depends on GSH/pH level and eventually causes tumor cell death. Our work makes the first attempt to reverse the function of GSH from ROS scavenger to ROS producer, explores new roles of PDA-based nanomaterials in CDT beyond photothermal reagents and drug carriers, and provides a new strategy to improve the efficiency of CDT.Statement of Significance P(DA-Fc) nanoparticles performing tumor microenvironment response capacity and tumor reductive power utilize ability were fabricated for CDT tumor suppression. After endocytosis by tumor cells, P(DA-Fc) deprived GSH of electrons for H2O2 and center dot OH release, mimicking the intrinsic ROS production con-ducted by NADPH, further inducing tumor cell necrosis and apoptosis. Our work makes the first attempt to reverse the function of GSH from ROS scavenger to producer, explores new functions of PDA-based nanomaterials in CDT beyond photothermal reagents and drug carriers, and provides a new strategy to improve CDT efficiency.(c) 2023 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:423 / 440
页数:18
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