Synergizing Pyroelectric Catalysis and Enzyme Catalysis: Establishing a Reciprocal and Synergistic Model to Enhance Anti-Tumor Activity

IF 27.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Materials Pub Date : 2024-02-27 DOI:10.1002/adma.202401111
Yan Wang, Rui Zhang, Pengyu Zang, Ruoxi Zhao, Linzhi Wu, Yanlin Zhu, Dan Yang, Shili Gai, Piaoping Yang
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Abstract

Nanozyme activity is greatly weakened by the microenvironment and multidrug resistance of tumor cells. Hence, a bi-catalytic nanoplatform, which promotes the anti-tumor activity through “charging empowerment” and “mutual complementation” processes involved in enzymatic and pyroelectric catalysis, by loading ultra-small nanoparticles (USNPs) of pyroelectric ZnSnO3 onto MXene nanozyme (V2CTx nanosheets), is developed. Here, the V2CTx nanosheets exhibit enhanced peroxidase activity by reacting V3+ with H2O2 to generate toxic ·OH, accelerated by the near-infrared (NIR) light mediated heat effect. The resulting V4+ is then converted to V3+ by oxidizing endogenous glutathione (GSH), realizing an enzyme-catalyzed cycle. However, the cycle will lose its persistence once GSH is insufficient; nevertheless, the pyroelectric charges generated by ZnSnO3 USNPs continuously support the V4+/V3+ conversion and ensure nanoenzyme durability. Moreover, the hyperthermia arising from the V2CTx nanosheets by NIR irradiation results in an ideal local temperature gradient for the ZnSnO3 USNPs, giving rise to an excellent pyroelectric catalytic effect by promoting band bending. Furthermore, polarized charges increase the tumor cell membrane permeability and facilitate nanodrug accumulation, thereby resolving the multidrug resistance issue. Thus, the combination of pyroelectric and enzyme catalysis together with the photothermal effect solves the dilemma of nanozymes and improves the antitumor efficiency.

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热释电催化与酶催化的协同作用:建立互惠协同模式以增强抗肿瘤活性
肿瘤细胞的微环境和多药耐药性会大大削弱纳米酶的活性。因此,我们开发了一种双催化纳米平台,通过在 MXene 纳米酶(V2CTx 纳米片)上负载热释电 ZnSnO3 的超小纳米颗粒(USNPs),在酶催化和热释电催化的 "充电赋能 "和 "互补 "过程中促进抗肿瘤活性。在这里,V2CTx 纳米片通过 V3+ 与 H2O2 反应生成有毒的 -OH,并在近红外(NIR)光介导的热效应下加速反应,从而显示出更强的过氧化物酶活性。生成的 V4+ 再通过氧化内源性谷胱甘肽(GSH)转化为 V3+,实现酶催化循环。然而,一旦谷胱甘肽不足,该循环就会失去持续性;不过,ZnSnO3 USNPs 产生的热释电荷可持续支持 V4+/V3+ 转换,并确保纳米酶的持久性。此外,在近红外照射下,V2CTx 纳米片产生的高热会使 ZnSnO3 USNPs 产生理想的局部温度梯度,从而通过促进带弯曲产生出色的热释电催化作用。此外,极化电荷还能增加肿瘤细胞膜的通透性,促进纳米药物的积累,从而解决多药耐药性问题。因此,热释电催化和酶催化与光热效应的结合解决了纳米酶的困境,提高了抗肿瘤效率。
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来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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