Beijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Adv Mater. 2024 Sep;36(38):e2406815. doi: 10.1002/adma.202406815. Epub 2024 Jul 31.
Dinuclear iridium(III) complexes activated by light-inducible spatiotemporal control are emerging as promising candidates for cancer therapy. However, broader applications of current light-activated dinuclear iridium(III) complexes are limited by the ineffective tissue penetration and undesirable feedback on guidance activation. Here, an ultrasound (US) triggered near infrared-fluorescent dinuclear iridium(III) nanoparticle, NanoIr, is first reported to precisely and spatiotemporally inhibit tumor growth. It is demonstrated that reactive oxygen species can be generated by NanoIr upon exposure to US irradiation (NanoIr + US), thereby inducing immunogenic cell death. When combined with cisplatin, NanoIr + US elicits synergistic effects in patient-derived tumor xenograft mice models of ovarian cancer. This work first provides a design of dinuclear iridium(III) nanoparticles for immunogenic sonodynamic therapy.
光诱导时空控制的双核铱(III)配合物作为癌症治疗的有前途的候选物正在兴起。然而,当前光激活双核铱(III)配合物的更广泛应用受到组织穿透性差和对引导激活的不良反馈的限制。在这里,首次报道了超声(US)触发的近红外荧光双核铱(III)纳米颗粒 NanoIr 可精确且时空地抑制肿瘤生长。研究表明,双核铱(III)纳米颗粒 NanoIr 在超声辐射下可产生活性氧(NanoIr + US),从而诱导免疫原性细胞死亡。当与顺铂联合使用时,NanoIr + US 在卵巢癌患者来源的肿瘤异种移植小鼠模型中产生协同作用。这项工作首次为免疫声动力学治疗设计了双核铱(III)纳米颗粒。