Yang Yuanqi, Xu Qingqing, Gu Wei, Nan Kaisheng, Chen Siyu, Wang Siling, Zhang Jinghai, Zhao Qinfu
Department of Microbial and Biochemical Pharmacy, School of Life Sciences and Biopharmaceuticals, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, Liaoning Province 110016, PR China.
Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, Liaoning Province 110016, PR China.
J Colloid Interface Sci. 2025 Apr;683(Pt 1):910-925. doi: 10.1016/j.jcis.2024.12.076. Epub 2024 Dec 13.
Photodynamic therapy (PDT) has witnessed remarkable progress in recent years owing to its specific properties. Given that the antioxidation system of tumor microenvironment (TME) adversely affects treatment outcomes, powerful TME modulators can significantly resolve the limitation of PDT. Herein, we developed a PEG-modified Cu-doped hollow mesoporous carbon nanozyme (CHC-PEG) and loaded insoluble photosensitizer IR780 into its pores and cavities to construct the multifunctional nano-system IR780/CHCP. CHC-PEG nanozyme could perform photothermal therapy (PTT) effect and protect IR780 from aggregation-caused quenching (ACQ) effect, while exerting peroxidase (POD)-mimetic activity and the ability of consuming glutathione (GSH) to achieve oxidative stress-augmented PDT effect. When exposed to near-infrared (NIR) light, IR780 was stimulated to produce singlet oxygen (O) and CHC-PEG could increase the temperature of TME to exert stronger POD-mimetic activity for producing more hydroxyl radicals (OH), therefore the IR780/CHCP nano-system exhibited remarkable tumor growth inhibition. Benefited by the enhanced synergistic effect, IR780/CHCP exhibited remarkable in vivo tumor growth inhibition, with the tumor inhibition rate of 93 %, and had no significant effect on major organs. Above all, IR780/CHCP could resist the antioxidant system in TME to enhance the level of oxidative stress, thereby enabling effective anti-tumor therapy. This study introduced a novel strategy to effectively promote the synergistic PTT/PDT effect by the enhanced oxidative stress.
近年来,光动力疗法(PDT)因其独特的性质取得了显著进展。鉴于肿瘤微环境(TME)的抗氧化系统会对治疗效果产生不利影响,强大的TME调节剂可以显著解决PDT的局限性。在此,我们开发了一种聚乙二醇(PEG)修饰的铜掺杂中空介孔碳纳米酶(CHC-PEG),并将不溶性光敏剂IR780负载到其孔腔中,构建了多功能纳米系统IR780/CHCP。CHC-PEG纳米酶可发挥光热疗法(PTT)作用,保护IR780免受聚集诱导猝灭(ACQ)效应的影响,同时发挥过氧化物酶(POD)模拟活性和消耗谷胱甘肽(GSH)的能力,以实现氧化应激增强的PDT效应。当暴露于近红外(NIR)光下时,IR780被激发产生单线态氧(O),CHC-PEG可提高TME的温度,以发挥更强的POD模拟活性,产生更多的羟基自由基(OH),因此IR780/CHCP纳米系统表现出显著的肿瘤生长抑制作用。得益于增强的协同效应,IR780/CHCP在体内表现出显著的肿瘤生长抑制作用,肿瘤抑制率为93%,且对主要器官无显著影响。最重要的是,IR780/CHCP可以抵抗TME中的抗氧化系统,提高氧化应激水平,从而实现有效的抗肿瘤治疗。本研究引入了一种新策略,通过增强氧化应激有效地促进PTT/PDT的协同效应。