"一石三鸟 "纳米平台:用于线粒体靶向光动力治疗缺氧性肿瘤的高效近红外触发 I 型 AIE 光敏剂

IF 13.9 Q1 CHEMISTRY, MULTIDISCIPLINARY
Shengnan Liu, Yu Pei, Yan Sun, Ziwei Wang, Haoran Chen, Dongxia Zhu, Martin R. Bryce, Ben Zhong Tang, Yulei Chang
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引用次数: 0

摘要

目前,有三大问题严重限制了癌症光动力疗法(PDT)的实际应用:(i) 肿瘤微环境(TME)缺氧;(ii) 聚集的有毒活性氧(ROS)生成效率低;(iii) 激发光的组织穿透深度浅。用单一设计解决上述三个问题的方法非常有限。本文展示了一种合理的 "一石三鸟 "分子和纳米工程策略:基于掺杂镧系元素的上转换纳米粒子(UCNPs)和具有 AIE 活性的二核 Ir(III)复合物的共价组合的光动力纳米平台 U-Ir@PAA-ABS,在 980 纳米波长的照射下,通过佛斯特共振能量转移(FRET)实现了低氧浓度依赖性的 I 型光化学过程。U-Ir@PAA-ABS 以线粒体为靶标,即使在严重缺氧环境下,经 980 纳米波长照射后也具有出色的光毒性,可诱导细胞凋亡和铁凋亡的双模式细胞死亡机制。综上所述,体外和体内研究结果表明,这是一种成功的策略,可提高光动力疗法对缺氧性肿瘤的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

“Three birds with one stone” nanoplatform: Efficient near-infrared-triggered type‑I AIE photosensitizer for mitochondria-targeted photodynamic therapy against hypoxic tumors

“Three birds with one stone” nanoplatform: Efficient near-infrared-triggered type‑I AIE photosensitizer for mitochondria-targeted photodynamic therapy against hypoxic tumors

“Three birds with one stone” nanoplatform: Efficient near-infrared-triggered type‑I AIE photosensitizer for mitochondria-targeted photodynamic therapy against hypoxic tumors

Currently three major problems seriously limit the practical application of cancer photodynamic therapy (PDT): (i) the hypoxic tumor microenvironment (TME); (ii) low generation efficiency of toxic reactive oxygen species (ROS) in aggregates and (iii) shallow tissue penetration depth of excitation light. Very limited approaches are available for addressing all the above three problems with a single design. Herein, a rational “three birds with one stone” molecular and nanoengineering strategy is demonstrated: a photodynamic nanoplatform U-Ir@PAA-ABS based on the covalent combination of lanthanide-doped upconversion nanoparticles (UCNPs) and an AIE-active dinuclear Ir(III) complex provides a low oxygen concentration-dependent type-I photochemical process upon 980 nm irradiation by Föster resonance energy transfer (FRET). U-Ir@PAA-ABS targets mitochondria and has excellent phototoxicity even in severe hypoxia environments upon 980 nm irradiation, inducing a dual-mode cell death mechanism by apoptosis and ferroptosis. Taken together, the in vitro and in vivo results demonstrate a successful strategy for improving the efficacy of PDT against hypoxic tumors.

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