Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, P. R. China.
Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
ACS Appl Mater Interfaces. 2024 Oct 30;16(43):58357-58369. doi: 10.1021/acsami.4c13687. Epub 2024 Oct 16.
Sonodynamic therapy (SDT) is a promising treatment modality for breast cancer; however, its effectiveness is often impeded by the hypoxic tumor microenvironment owing to an insufficient oxygen supply in the solid tumors. To overcome this challenge, we elaborately developed a 4T1 tumor-targeted multifunctional nanoagent by integrating both dendrimer-structured copper chelating agents and organic sonosensitizers (IR820) into a biotin-modified nanoliposome via a microfluidic-assisted self-assembly. In particular, the aforementioned copper chelating agent was constructed by introducing multiple xanthate groups into a dendrimer polymer, which showed a significant selectivity for the consumption of the intracellular copper levels. Based on this, the nanoliposome-based therapeutic not only disrupted the activity of the mitochondrial complex IV to directly inhibit the tumor cell proliferation but also suppressed the resistance to the SDT via inhibition of the oxygen consumption for cellular respiration. Both and studies confirmed that the designed nanoagents exhibit a synergistic tumor inhibition effect of copper consumption and IR820-mediated SDT. Taken together, this approach establishes a proof-of-concept for the construction of a copper-ion-modulated nanomedicine to significantly enhance the efficiency of oxygen-dependent cancer treatments.
声动力学疗法(SDT)是一种有前途的乳腺癌治疗方式;然而,由于实体肿瘤中氧气供应不足,其效果常常受到缺氧肿瘤微环境的阻碍。为了克服这一挑战,我们通过微流控辅助自组装,将树枝状结构的铜螯合剂和有机声敏剂(IR820)整合到生物素修饰的脂质体中,精心开发了一种 4T1 肿瘤靶向多功能纳米制剂。具体来说,上述铜螯合剂是通过在树枝状聚合物中引入多个黄原酸基团构建的,它对细胞内铜水平的消耗表现出显著的选择性。基于此,基于脂质体的治疗不仅破坏了线粒体复合物 IV 的活性,直接抑制肿瘤细胞增殖,还通过抑制细胞呼吸对氧气的消耗来抑制对 SDT 的耐药性。和 研究均证实,所设计的纳米制剂表现出铜消耗和 IR820 介导的 SDT 的协同肿瘤抑制作用。综上所述,该方法为构建铜离子调节的纳米药物以显著提高依赖氧的癌症治疗效率建立了概念验证。