Cai Lihan, Sun Tao, Han Fuping, Zhang Han, Zhao Jiyu, Hu Qiao, Shi Tiancong, Zhou Xiao, Cheng Fang, Peng Chong, Zhou Ye, Long Saran, Sun Wen, Fan Jiangli, Du Jianjun, Peng Xiaojun
State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, Dalian University of Technology, Dalian 116024, P. R. China.
Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen 518060, P. R. China.
J Am Chem Soc. 2024 Dec 11;146(49):34188-34198. doi: 10.1021/jacs.4c14489. Epub 2024 Nov 24.
Piezoelectric materials can generate charges and reactive oxygen species (ROS) under external force stimulation for ultrasound-induced sonodynamic therapy (SDT). However, their poor piezoelectricity, fast electron-hole pair recombination rate, and biological toxicity of piezoelectric materials limit the therapeutic effects of piezoelectric SDT. In this study, hollow ZnO (HZnO) nanospheres were synthesized by using a one-step method. The hollow structure facilitated the deformation of HZnO under stimulation by ultrasound mechanical force and increased the piezoelectric constant. Subsequently, black phosphorus quantum dots (BPQDs) and arginine-glycine-aspartic acid peptide (RGD)-poly(ethylene glycol) (PEG) were combined with HZnO to further enhance the piezoelectric effect by constructing heterojunctions and enable tumor-targeting ability. During treatment, HZnO-BPQDs-PEG could degrade in an acidic tumor microenvironment and release Zn and PO ions to induce pro-death autophagy. The ROS produced by SDT also accelerated autophagy and promoted ferroptosis in cancer cells. This study demonstrates that HZnO-BPQDs-PEG has a strong piezoelectric SDT effect and can effectively induce autophagy in cancer cells, providing a new idea for the design and application of piezoelectric materials for tumor therapy.
压电材料在外力刺激下可产生电荷和活性氧(ROS),用于超声诱导的声动力疗法(SDT)。然而,它们较差的压电性、快速的电子 - 空穴对复合率以及压电材料的生物毒性限制了压电SDT的治疗效果。在本研究中,采用一步法合成了中空ZnO(HZnO)纳米球。中空结构促进了HZnO在超声机械力刺激下的变形,并提高了压电常数。随后,将黑磷量子点(BPQDs)和精氨酸 - 甘氨酸 - 天冬氨酸肽(RGD) - 聚乙二醇(PEG)与HZnO结合,通过构建异质结进一步增强压电效应,并赋予肿瘤靶向能力。在治疗过程中,HZnO - BPQDs - PEG可在酸性肿瘤微环境中降解并释放Zn和PO离子以诱导促死亡自噬。SDT产生的ROS也加速了自噬并促进癌细胞的铁死亡。本研究表明,HZnO - BPQDs - PEG具有强大的压电SDT效应,可有效诱导癌细胞自噬,为肿瘤治疗的压电材料设计与应用提供了新思路。