School of Biomedical Engineering, Anhui Medical University, Hefei, 230032, P. R. China.
School of Pharmacy, Anhui Medical University, Hefei, 230032, P. R. China.
Adv Healthc Mater. 2023 Aug;12(20):e2300012. doi: 10.1002/adhm.202300012. Epub 2023 Mar 31.
The development of nanomedicines that combine photothermal therapy (PTT) with photodynamic therapy (PDT) is considered promising for cancer treatment, but still faces the challenge of enhancing tumoricidal efficiency. Fortunately, apart from the well-acknowledged effect on direct tumor cell-killing, nitric oxide (NO) is also considered to be effective for the enhancement of both PTT and PDT. However, both the low loading efficiency of NO precursor and the short half-life time and diffusion distance of NO hamper the synergistic therapeutic efficacy of NO. Taking the aforementioned factors into account, a mitochondria-targeted nitric oxide nanogenerator, EArgFe@Ce6, is constructed to achieve high loading of the NO donor l-Arginine (l-Arg) for synergistic photodynamic/gas/photothermal therapy upon single 660 nm light irradiation. The coordination of epigallocatechin gallate (EGCG) and ferric ions (Fe ) provides EArgFe@Ce6 supreme photothermal capability to perform low-temperature PTT (mPTT). EGCG endows EArgFe@Ce6 with mitochondria-targeting capability and meanwhile favors hypoxia alleviation for enhanced PDT. The PDT-produced massive reactive oxygen species (ROS) further catalyzes l-Arg to generate a considerable amount of NO to perform gas therapy and sensitize both mPTT and PDT. In vitro and in vivo studies demonstrate that the synergistic photodynamic/gas/photothermal therapy triggered by single 660 nm light irradiation is highly effective for tumor treatments.
将光热疗法(PTT)与光动力疗法(PDT)相结合的纳米医学的发展被认为是癌症治疗的有前途的方法,但仍面临着提高肿瘤杀伤效率的挑战。幸运的是,除了众所周知的直接杀伤肿瘤细胞的作用外,一氧化氮(NO)也被认为对 PTT 和 PDT 的增强有效。然而,NO 前体的低负载效率以及 NO 的半衰期和扩散距离短,阻碍了 NO 的协同治疗效果。考虑到上述因素,构建了一种靶向线粒体的一氧化氮纳米发生器 EArgFe@Ce6,以实现在 660nm 单光照射下协同光动力/气体/光热治疗的高负载 NO 供体 l-精氨酸(l-Arg)。没食子酸表儿茶素(EGCG)和铁离子(Fe )的配位为 EArgFe@Ce6 提供了卓越的光热能力,以进行低温 PTT(mPTT)。EGCG 赋予 EArgFe@Ce6 靶向线粒体的能力,同时有利于缓解缺氧以增强 PDT。PDT 产生的大量活性氧(ROS)进一步催化 l-Arg 生成相当数量的 NO 以进行气体治疗,并敏化 mPTT 和 PDT。体外和体内研究表明,由 660nm 单光激发引发的协同光动力/气体/光热治疗对肿瘤治疗非常有效。