Yang Han, Li Xueyu, Wang Qian, Yang Fujun, Zhong Xiaoyuan, Gu Liping, Miao Yuqing, Liu Baolin, Li Yuhao
School of Materials and Chemistry, Institute of Bismuth Science, University of Shanghai for Science and Technology, Shanghai 200093, China.
Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai 200433, China.
J Colloid Interface Sci. 2025 Mar;681:319-330. doi: 10.1016/j.jcis.2024.11.168. Epub 2024 Nov 23.
Artificially synthesized nanozymes exhibit enzymatic activity similar to that of natural enzymes. However, in the complex tumor microenvironment, their diversity and catalytic activity show significant variations, limiting their effectiveness in catalytic therapy. Developing artificial enzymes with multiple enzymatic activities and spatiotemporal controllable catalytic abilities is of great clinical significance. Herein, we propose a novel strategy for synergistic enzyme catalysis and sonocatalytic therapy of tumors using polyoxometalates-based nanozymes. Copper-doped molybdenum-based polyoxometalates (denoted as CP) were rapidly synthesized at room temperature through a one-step method. CP contains mixed-valence states of Cu/Cu and Mo/Mo ions, endowing it with enzyme-like activities of peroxidase, catalase, and glutathione peroxidase. Additionally, the incorporation of copper ions introduces oxygen vacancies into the nano-polyoxometalate, which not only reduces the bandgap but also enhances carrier separation efficiency, thereby improving the sonocatalytic performance of CP as a semiconductor. The combined effects of enzyme-like catalysis and sonocatalysis generate multiple reactive oxygen species (ROS), synergistically depleting glutathione (GSH) and disrupting the redox homeostasis of the tumor, inducing ferroptosis in tumor cells and thereby inhibiting tumor proliferation. This study provides new insights into the design of artificial nanozymes with multiple enzymatic activities and ultrasound activation functions for combined tumor therapy.
人工合成的纳米酶表现出与天然酶相似的酶活性。然而,在复杂的肿瘤微环境中,它们的多样性和催化活性存在显著差异,限制了它们在催化治疗中的有效性。开发具有多种酶活性和时空可控催化能力的人工酶具有重要的临床意义。在此,我们提出了一种使用基于多金属氧酸盐的纳米酶进行肿瘤协同酶催化和声催化治疗的新策略。通过一步法在室温下快速合成了铜掺杂的钼基多金属氧酸盐(记为CP)。CP含有Cu/Cu和Mo/Mo离子的混合价态,赋予其过氧化物酶、过氧化氢酶和谷胱甘肽过氧化物酶等类酶活性。此外,铜离子的掺入在纳米多金属氧酸盐中引入了氧空位,这不仅降低了带隙,还提高了载流子分离效率,从而提高了CP作为半导体的声催化性能。类酶催化和声催化的联合作用产生多种活性氧(ROS),协同消耗谷胱甘肽(GSH)并破坏肿瘤的氧化还原稳态,诱导肿瘤细胞发生铁死亡,从而抑制肿瘤增殖。本研究为设计具有多种酶活性和超声激活功能的人工纳米酶用于联合肿瘤治疗提供了新的见解。