Mn-single-atom nano-multizyme enabled NIR-II photoacoustically monitored, photothermally enhanced ROS storm for combined cancer therapy.

IF 8.1 Q1 ENGINEERING, BIOMEDICAL Biomaterials research Pub Date : 2023-12-04 DOI:10.1186/s40824-023-00464-w
Xiaozhe Wang, Xiaofeng Ren, Jie Yang, Zican Zhao, Xiaoyu Zhang, Fan Yang, Zheye Zhang, Peng Chen, Liping Li, Ruiping Zhang
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Abstract

Rationale: To realize imaging-guided multi-modality cancer therapy with minimal side effects remains highly challenging.

Methods: We devised a bioinspired hollow nitrogen-doped carbon sphere anchored with individually dispersed Mn atoms (Mn/N-HCN) via oxidation polymerization with triton micelle as a soft template, followed by carbonization and annealing. Enzyme kinetic analysis and optical properties were performed to evaluate the imaging-guided photothermally synergized nanocatalytic therapy.

Results: Simultaneously mimicking several natural enzymes, namely peroxidase (POD), catalase (CAT), oxidase (OXD), and glutathione peroxidase (GPx), this nano-multizyme is able to produce highly cytotoxic hydroxyl radical (•OH) and singlet oxygen (1O2) without external energy input through parallel and series catalytic reactions and suppress the upregulated antioxidant (glutathione) in tumor. Furthermore, NIR-II absorbing Mn/N-HCN permits photothermal therapy (PTT), enhancement of CAT activity, and photoacoustic (PA) imaging to monitor the accumulation kinetics of the nanozyme and catalytic process in situ. Both in vitro and in vivo experiments demonstrate that near-infrared-II (NIR-II) PA-imaging guided, photothermally enhanced and synergized nanocatalytic therapy is efficient to induce apoptosis of cancerous cells and eradicate tumor tissue.

Conclusions: This study not only demonstrates a new method for effective cancer diagnosis and therapy but also provides new insights into designing multi-functional nanozymes.

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mn -单原子纳米多酶使NIR-II光声监测,光热增强ROS风暴用于联合癌症治疗。
基本原理:实现成像引导的多模式肿瘤治疗与最小的副作用仍然是非常具有挑战性的。方法:以triton胶束为软模板,通过氧化聚合,设计了一种由分散的Mn原子(Mn/N-HCN)锚定的生物空心氮掺杂碳球,然后进行碳化和退火。通过酶动力学分析和光学性质对成像引导光热协同纳米催化疗法进行评价。结果:该纳米多酶能同时模拟几种天然酶,即过氧化物酶(POD)、过氧化氢酶(CAT)、氧化酶(OXD)和谷胱甘肽过氧化物酶(GPx),无需外部能量输入即可通过平行和串联催化反应产生高细胞毒性的羟基自由基(•OH)和谷胱甘肽过氧化物酶(1O2),抑制肿瘤中上调的抗氧化剂(谷胱甘肽)。此外,NIR-II吸收Mn/N-HCN允许光热治疗(PTT),增强CAT活性和光声成像(PA),以监测纳米酶的积累动力学和原位催化过程。体外和体内实验均表明,近红外- ii (NIR-II) pa成像引导、光热增强和协同纳米催化治疗可有效诱导癌细胞凋亡和根除肿瘤组织。结论:本研究不仅为癌症的有效诊断和治疗提供了新的方法,而且为设计多功能纳米酶提供了新的思路。
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