双功能
声动力疗法
材料科学
体内
生物相容性
体外
肿瘤缺氧
癌症研究
纳米技术
生物物理学
免疫疗法
医学
免疫系统
活性氧
放射治疗
免疫学
生物化学
催化作用
生物
化学
内科学
冶金
生物技术
作者
Chao Li,Yucong Gao,Yuanyue Wang,Jie Wang,Jiao‐Min Lin,Jing Du,Zhiguo Zhou,Xiaoming Liu,Shiping Yang,Hong Yang
标识
DOI:10.1002/adfm.202210348
摘要
Abstract Alleviating the hypoxia of tumor cells would be an effective strategy to improve the efficiency of sonodynamic therapy (SDT). Here, an Ir(III) phthalocyanine complex (IrPc) is synthesized and characterized, with which a nano‐assembly (IrPc‐NPs) is prepared by encapsulating its aggregates with BSA. IrPc‐NPs exhibit bifunctionality, catalysis on H 2 O 2 decomposition to evolve O 2, and sonosensitization to generate 1 O 2 both in vitro and in vivo. The bifunctionality concertedly and synergistically boosts the efficacy of SDT by alleviating the hypoxia of tumor cells. Its amplifying effect on photoacoustic signal provides a tool to monitor the accumulation of the nano‐assembly in a tumor that guides timely the application of ultrasonic (US) irradiation during SDT treatment. These results also suggest that immunogenic cell death‐mediated immunotherapy for tumor cells is attributed to the efficacy of SDT induced by IrPc‐NPs. IrPc‐NPs exhibit excellent biocompatibility in vitro, benignancy in vivo toward the overall growth of the tumor‐bearing mice inoculated with 4T1 cells and the controllability on timely applying US irradiation during their treatment with IrPc‐NPs renders the nanosystem great potentials in developing into a clinic drug for immunogenic sonodynamic therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI