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用于原位乳腺癌多模态光热诊疗的近红外二区聚集诱导发光分子的多维供体工程

Multi-dimensional donor engineering of NIR-II AIEgens for multimodal phototheranostics of orthotopic breast cancer.

作者信息

Yuan Tao, Cui Jie, Zhu Jun, Mei Ju, Wang Dong, Hua Jianli

机构信息

Key Laboratory for Advanced Materials and Joint International Research Laboratory for Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, China.

Center for AIE Research, Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Materials Science and Engineering, Shenzhen University, Shenzhen, 518060, China; School of Pharmacy, Guangdong Medical University, Dongguan, 523808, China.

出版信息

Biomaterials. 2025 Aug;319:123193. doi: 10.1016/j.biomaterials.2025.123193. Epub 2025 Feb 19.

Abstract

"One-for-all" multimodal phototheranostic agents, which integrate multiple photodiagnostic and phototherapeutic functionalities into a single component, have emerged as promising platforms for advancing cancer treatment. Among these, agents featuring second near-infrared (NIR-II) emission are particularly appealing due to their superior tissue penetration depth and high signal-to-background ratio (SBR). However, most reported NIR-II fluorophores suffer from severely imbalanced radiative and non-radiative excited-state energy dissipation in biological environments, resulting in extremely low fluorescence quantum yields (QYs) and limited diagnostic efficacy. This highlights the urgent need for innovative molecular design strategies to develop high-performance NIR-II "one-for-all" multimodal phototheranostic agents. Herein, we present, for the first time, a multi-dimensional donor engineering protocol that optimizes donor design at the molecular, aggregated, and solvent-interaction levels. By introducing 2,4,4-trimethylpentan-2-yl groups into the diphenylamine indeno[1,2-b]thiophene donor unit, we developed a donor-acceptor-donor (D-A-D) type NIR-II aggregation-induced emission-active luminogen (AIEgen), i.e. OPITBT. When formulated into nanoparticles (NPs), OPITBT NPs exhibited a 16-fold enhancement in fluorescence QY compared to OPITBT in tetrahydrofuran, along with excellent photothermal conversion efficiency (PCE) and acceptable type-I reactive oxygen species (ROS) generation. When further fabricated into tumor-targeting NPs, the resulted OPITBT-R NPs effectively eliminated orthotopic breast cancer through fluorescence-photoacoustic-photothermal multimodal imaging-guided photodynamic-photothermal synergistic therapy under single 808 nm laser irradiation. Notably, the exceptional NIR-II fluorescence brightness of OPITBT-R NPs enables high-resolution NIR-IIb whole-body vascular imaging in living mice. This work provides a versatile strategy to enhance radiative dissipation of NIR-II fluorophores for balanced phototheranostic performance and advances the development of "one-for-all" phototheranostic systems.

摘要

“一药多用”的多模态光诊疗剂将多种光诊断和光治疗功能集成于单一组件中,已成为推进癌症治疗的有前景的平台。其中,具有第二近红外(NIR-II)发射特性的试剂因其卓越的组织穿透深度和高信背比(SBR)而格外引人注目。然而,大多数已报道的NIR-II荧光团在生物环境中存在辐射和非辐射激发态能量耗散严重失衡的问题,导致荧光量子产率(QYs)极低,诊断效果有限。这凸显了迫切需要创新的分子设计策略来开发高性能的NIR-II“一药多用”多模态光诊疗剂。在此,我们首次提出一种多维供体工程方案,该方案在分子、聚集和溶剂相互作用水平上优化供体设计。通过将2,4,4-三甲基戊烷-2-基引入二苯胺茚并[1,2-b]噻吩供体单元,我们开发了一种供体-受体-供体(D-A-D)型NIR-II聚集诱导发光活性发光体(AIEgen),即OPITBT。当制备成纳米颗粒(NPs)时,与OPITBT在四氢呋喃中的情况相比,OPITBT NPs的荧光QY提高了16倍,同时具有优异的光热转换效率(PCE)和可接受的I型活性氧(ROS)生成能力。当进一步制备成肿瘤靶向NPs时,所得的OPITBT-R NPs在单次808 nm激光照射下,通过荧光-光声-光热多模态成像引导的光动力-光热协同治疗有效地消除了原位乳腺癌。值得注意的是,OPITBT-R NPs出色地NIR-II荧光亮度使得在活体小鼠中能够进行高分辨率的NIR-IIb全身血管成像。这项工作提供了一种通用策略来增强NIR-II荧光团的辐射耗散,以实现平衡的光诊疗性能,并推动了“一药多用”光诊疗系统的发展。

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