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具有多种类酶活性的氧化锰修饰氯氧化铋压电纳米平台用于癌症声动力治疗

Manganese oxide-modified bismuth oxychloride piezoelectric nanoplatform with multiple enzyme-like activities for cancer sonodynamic therapy.

作者信息

Zhao Yunchao, Huang Tian, Wang Shaobo, Yao Shuncheng, Hu Quanhong, Wan Xingyi, Guo Ning, Zhang Yang, Li Linlin

机构信息

Beijing Institute of Nanoenergy and Nanosystems, Chinese Academy of Sciences, Beijing 100140, PR China; Center on Nanoenergy Research, School of Physical Science and Technology, Guangxi University, Nanning 530004, PR China.

Beijing Institute of Nanoenergy and Nanosystems, Chinese Academy of Sciences, Beijing 100140, PR China; Center on Nanoenergy Research, School of Physical Science and Technology, Guangxi University, Nanning 530004, PR China; School of Nanoscience and Technology, University of Chinese Academy of Sciences, Beijing 100049, PR China.

出版信息

J Colloid Interface Sci. 2023 Jun 15;640:839-850. doi: 10.1016/j.jcis.2023.03.008. Epub 2023 Mar 7.

Abstract

Sonodynamic therapy (SDT) is considered as a new-rising strategy for cancer therapeutics, but the inefficient production of reactive oxygen species (ROS) by current sonosensitizers seriously hinders its further applications. Herein, a piezoelectric nanoplatform is fabricated for enhancing SDT against cancer, in which manganese oxide (MnO) with multiple enzyme-like activities is loaded on the surface of piezoelectric bismuth oxychloride nanosheets (BiOCl NSs) to form a heterojunction. When exposed to ultrasound (US) irradiation, piezotronic effect can remarkably promote the separation and transport of US-induced free charges, and further enhance ROS generation in SDT. Meanwhile, the nanoplatform shows multiple enzyme-like activities from MnO, which can not only downregulate the intracellular glutathione (GSH) level, but also disintegrate endogenous hydrogen peroxide (HO) to generate oxygen (O) and hydroxyl radicals (•OH). As a result, the anticancer nanoplatform substantially boosts ROS generation and reverses tumor hypoxia. Ultimately, it reveals remarkable biocompatibility and tumor suppression in a murine model of 4 T1 breast cancer under US irradiation. This work provides a feasible pathway for improving SDT using piezoelectric platforms.

摘要

声动力疗法(SDT)被认为是一种新兴的癌症治疗策略,但目前的声敏剂产生活性氧(ROS)的效率低下,严重阻碍了其进一步应用。在此,制备了一种压电纳米平台以增强针对癌症的SDT,其中具有多种类酶活性的氧化锰(MnO)负载在压电氯氧化铋纳米片(BiOCl NSs)表面以形成异质结。当暴露于超声(US)照射时,压电子效应可显著促进US诱导的自由电荷的分离和传输,并进一步增强SDT中ROS的产生。同时,该纳米平台表现出MnO的多种类酶活性,其不仅可以下调细胞内谷胱甘肽(GSH)水平,还可以分解内源性过氧化氢(HO)以产生氧气(O)和羟基自由基(•OH)。结果,抗癌纳米平台大幅提高ROS的产生并逆转肿瘤缺氧。最终,它在US照射下的4T1乳腺癌小鼠模型中显示出显著的生物相容性和肿瘤抑制作用。这项工作为使用压电平台改善SDT提供了一条可行的途径。

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