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用于协同催化治疗的二维多孔蛭石基纳米催化剂

Two-dimensional porous vermiculite-based nanocatalysts for synergetic catalytic therapy.

作者信息

Nie Yichu, Chen Wei, Kang Yong, Yuan Xue, Li Yongjiang, Zhou Jun, Tao Wei, Ji Xiaoyuan

机构信息

Clinical Research Institute, First People's Hospital of Foshan, Foshan, Guangdong, 528000, China.

Center for Nanomedicine and Department of Anesthesiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Biomaterials. 2023 Apr;295:122031. doi: 10.1016/j.biomaterials.2023.122031. Epub 2023 Jan 28.

Abstract

This study reports an ultrasound-mediated and two-dimensional (2D) porous vermiculite nanosheets (VMT NSs)-based nanocatalyst platform (Arg@VMT@PDA-PEG) that synergistically harnessed the Fenton reaction-based chemodynamic therapy (CDT), 2D semiconductor-based sonodynamic therapy (SDT) and nitric oxide (NO)-based gas therapy for combination cancer therapy. The tumor microenvironment responsive degradation of polydopamine (PDA) shell could not only prevent L-Arg, a NO donor, leakage during blood circulation, but also selectively release the active sites of VMT NSs for catalytic reactions in tumor cells. Additionally, the Fenton reactions mediated by the abundant Fe/Fe in VMT NSs could efficiently produce ·OH and consume glutathione (GSH) for CDT. Moreover, the reactive oxygen species (ROS, ·OH and ·O) produced by ultrasound-triggered Arg@VMT@PDA-PEG could not only execute SDT but also oxidize L-Arg to NO for synergetic gas therapy. The results show that the transformation of ROS to NO can enhance curative efficacy owing to the ability of NO with much longer life-time in freely diffusing into cells from intercellular space. This biodegradable Arg@VMT@PDA-PEG nanocatalytic platform integrating three different catalytic reactions provides a new therapeutic paradigm for combination cancer therapy.

摘要

本研究报道了一种基于超声介导和二维(2D)多孔蛭石纳米片(VMT NSs)的纳米催化剂平台(Arg@VMT@PDA-PEG),该平台协同利用基于芬顿反应的化学动力疗法(CDT)、基于二维半导体的声动力疗法(SDT)和基于一氧化氮(NO)的气体疗法进行联合癌症治疗。聚多巴胺(PDA)壳的肿瘤微环境响应性降解不仅可以防止NO供体L-精氨酸(L-Arg)在血液循环过程中泄漏,还可以选择性地释放VMT NSs的活性位点以在肿瘤细胞中进行催化反应。此外,VMT NSs中丰富的Fe/Fe介导的芬顿反应可以有效地产生·OH并消耗谷胱甘肽(GSH)用于CDT。此外,超声触发的Arg@VMT@PDA-PEG产生的活性氧(ROS,·OH和·O)不仅可以执行SDT,还可以将L-Arg氧化为NO用于协同气体治疗。结果表明,由于NO具有更长的寿命,能够从细胞间空间自由扩散到细胞中,ROS向NO的转化可以提高治疗效果。这种整合三种不同催化反应的可生物降解的Arg@VMT@PDA-PEG纳米催化平台为联合癌症治疗提供了一种新的治疗模式。

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