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用于超声触发和线粒体靶向的压电动力学癌症治疗的压电催化 2D WS 纳米片协同能量代谢靶向化疗。

Piezocatalytic 2D WS Nanosheets for Ultrasound-Triggered and Mitochondria-Targeted Piezodynamic Cancer Therapy Synergized with Energy Metabolism-Targeted Chemotherapy.

机构信息

Department of Nano-Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.

Department of Materials Science and Engineering, Gachon University, Seongnam, Gyeonggi-Do, 13306, Republic of Korea.

出版信息

Adv Mater. 2023 May;35(18):e2300437. doi: 10.1002/adma.202300437. Epub 2023 Mar 24.

DOI:10.1002/adma.202300437
PMID:36780270
Abstract

Piezoelectric nanomaterials that can generate reactive oxygen species (ROS) by piezoelectric polarization under an external mechanical force have emerged as an effective platform for cancer therapy. In this study, piezoelectric 2D WS nanosheets are functionalized with mitochondria-targeting triphenylphosphonium (TPP) for ultrasound (US)-triggered, mitochondria-targeted piezodynamic cancer therapy. In addition, a glycolysis inhibitor (FX11) that can inhibit cellular energy metabolism is loaded into TPP- and poly(ethylene glycol) (PEG)-conjugated WS nanosheet (TPEG-WS ) to potentiate its therapeutic efficacy. Upon US irradiation, the sono-excited electrons and holes generated in the WS are efficiently separated by piezoelectric polarization, which subsequently promotes the production of ROS. FX11-loaded TPEG-WS (FX11@TPEG-WS ) selectively accumulates in the mitochondria of human breast cancer cells. In addition, FX11@TPEG-WS effectively inhibits the production of adenosine triphosphate . Thus, FX11@TPEG-WS exhibits outstanding anticancer effects under US irradiation. An in vivo study using tumor-xenograft mice demonstrates that FX11@TPEG-WS effectively accumulated in the tumors. Its tumor accumulation is visualized using in vivo computed tomography . Notably, FX11@TPEG-WS with US irradiation remarkably suppresses the tumor growth of mice without systemic toxicity. This study demonstrates that the combination of piezodynamic therapy and energy metabolism-targeted chemotherapy using mitochondria-targeting 2D WS is a novel strategy for the selective and effective treatment of tumors.

摘要

压电纳米材料在外力作用下通过压电极化可以产生活性氧物种 (ROS),因此成为癌症治疗的有效平台。在这项研究中,二维二硫化钨 (WS) 纳米片通过靶向线粒体的三苯基膦 (TPP) 功能化,用于超声 (US) 触发、靶向线粒体的压动动力学癌症治疗。此外,负载了一种可以抑制细胞能量代谢的糖酵解抑制剂 (FX11) 的 TPP 和聚乙二醇 (PEG) 修饰的 WS 纳米片 (TPEG-WS) 可以增强其治疗效果。在 US 照射下,WS 中产生的电子和空穴被压电极化有效分离,随后促进 ROS 的产生。负载 FX11 的 TPEG-WS (FX11@TPEG-WS) 选择性地积聚在人乳腺癌细胞的线粒体中。此外,FX11@TPEG-WS 有效地抑制了三磷酸腺苷的产生。因此,在 US 照射下,FX11@TPEG-WS 表现出出色的抗癌效果。使用肿瘤异种移植小鼠的体内研究表明,FX11@TPEG-WS 有效地积聚在肿瘤中。其肿瘤积聚可以通过体内计算机断层扫描可视化。值得注意的是,US 照射下的 FX11@TPEG-WS 显著抑制了小鼠的肿瘤生长,而没有全身毒性。这项研究表明,使用靶向线粒体的二维 WS 的压动动力学治疗与能量代谢靶向化疗的结合是一种选择性和有效治疗肿瘤的新策略。

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