Biomimetic redox-responsive prodrug micelles with diselenide linkage for platinum nanozymes augmented sonodynamic/chemo combined therapy of colon cancer

声动力疗法 前药 胶束 体内 癌症研究 化学 药理学 生物物理学 组合化学 细胞凋亡 医学 生物化学 水溶液 生物 有机化学 生物技术
作者
Yuanru Zhao,Jingwen Xu,Yuanyuan Zhang,Feng Wu,Wei Zhao,Runqing Li,Yun Yang,Mingzhen Zhang,Yujie Zhang,Cheng Guo
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:472: 144911-144911 被引量:25
标识
DOI:10.1016/j.cej.2023.144911
摘要

Due to the complexity of tumorigenesis, it is hard to completely cure tumors with a single tumor therapy. Combined sonodynamic therapy and chemotherapy (sono-chemotherapy) based on the stimulus-responsive nano-delivery system is a prospective antitumor strategy that has demonstrated synergistic treatment effects and higher treatment effects than any monotherapy. The multiple diselenide linkages-contained DSeDP-alt-PEG conjugated with Ce6/PTX to yield prodrugs DC and DP micelles, and platinum nanozymes that possessed multiple enzyme activities were loaded in DC to form stable micelles (DC@Pt). The nanomicelles were modified with the homologous tumor cell membrane (DPC@Pt@M) to generate a REDOX-responsive bionic nanoplatform to realize the sono-chemotherapy combined treatment for colon cancer. As a redox-responsive nanoplatform, DPC@Pt@M exhibited excellent water solubility and bioavailability, and good targeting ability both in vitro and in vivo to realize the controlled release of Ce6 and PTX at the tumor site. Pt nanozymes acted as a cascade catalyst (SOD-CAT, SOD-POD) to alleviate hypoxia and improve SDT. Under ultrasonic irradiation, the novel micelle DPC@Pt@M increased ROS production and induced apoptosis efficiently in vitro and in vivo to improve sono-chemotherapeutic efficiency for colon cancer. Therefore, sonodynamic/chemo therapies demonstrated a clear synergistic effect, and this research is expected to provide a paradigm of combination therapy strategies for colon cancer.
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