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氧化还原活性多酚纳米颗粒剥夺内源性谷胱甘肽的电子以产生 ROS 并进行肿瘤化学动力学治疗。

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

机构信息

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Material Science and Engineering, Frontiers Science Center for Materiobiology and Dynamic Chemistry, East China University of Science and Technology, Shanghai 200237, PR China.

State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Key Laboratory for Advanced Materials and Joint International Research Laboratory for Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Centre for Computational Chemistry and Research Institute of Industrial Catalysis, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, PR China.

出版信息

Acta Biomater. 2023 Dec;172:423-440. doi: 10.1016/j.actbio.2023.09.037. Epub 2023 Sep 30.

Abstract

Chemodynamic therapy (CDT) based on generating reactive oxygen species (ROS) is promising for cancer treatment. However, the intrinsic HO is deficient for CDT, and glutathione (GSH) eliminates ROS to protect tumor cells from ROS cytotoxicity. Herein, we propose a strategy to switch the electron flow direction of GSH for O 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 for HO generation; the following •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 produce 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 HO and •OH release, mimicking the intrinsic ROS production conducted 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.

摘要

基于生成活性氧 (ROS) 的化学动力学疗法 (CDT) 有望用于癌症治疗。然而,内源性 HO 对 CDT 不足,谷胱甘肽 (GSH) 消除 ROS 以保护肿瘤细胞免受 ROS 细胞毒性。在此,我们提出了一种策略,通过使用聚多巴胺 (PDA) 接枝的二茂铁羧酸 (Fc) 聚合物 P(DA-Fc) 纳米粒子,将 GSH 的电子流方向从 O 还原和 ROS 生成而不是 ROS 清除切换,该纳米粒子具有酚醌转化能力,可以模拟 NOX 酶从 GSH 剥夺电子以还原 O 生成 HO;随后 Fc 可以触发 •OH 释放。GSH 处理后,P(DA-Fc) 中的半醌自由基显著增强,通过计算进一步证明了其具有很强的单电子还原能力。体外和体内实验表明,P(DA-Fc) 可以消耗内源性 GSH 产生内源性 ROS;ROS 的生成强烈依赖于 GSH/pH 水平,最终导致肿瘤细胞死亡。我们的工作首次尝试将 GSH 的功能从 ROS 清除剂转变为 ROS 产生剂,探索了基于 PDA 的纳米材料在 CDT 中的除光热试剂和药物载体之外的新作用,并提供了提高 CDT 效率的新策略。

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