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用于近红外-II双光子光动力疗法的具有近红外-I聚集诱导发光的线粒体锚定光敏剂

Mitochondrion-Anchored Photosensitizer with Near Infrared-I Aggregation-Induced Emission for Near Infrared-II Two-Photon Photodynamic Therapy.

作者信息

He Zhenyan, Gao Yuting, Zhang Huimin, Xue Ying, Meng Fanling, Luo Liang

机构信息

National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.

Engineering Research Center of Nano-Geomaterials of the Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, 430074, P. R. China.

出版信息

Adv Healthc Mater. 2021 Dec;10(24):e2101056. doi: 10.1002/adhm.202101056. Epub 2021 Sep 26.

Abstract

Two-photon photodynamic therapy (2P-PDT) that employs photosensitizers (PSs) with 2P absorption is particularly intriguing in cancer treatment, in that 2P excitation enables precise spatial localization and deep tissue penetration. Here, a donor-π-acceptor PS (named TPBPy) with near infrared (NIR) aggregation-induced emission (AIE) is designed and synthesized for imaging-guided 2P-PDT. The maximal photoluminescence (PL) peak of TPBPy is as high as 720 nm when it is encapsulated in liposomes. Upon 2P irradiation by a laser in NIR-II window (λ = 1000 nm), TPBPy exhibits strong NIR-I PL in a multicellular tumor spheroids (MCTSs) model, showing an imaging depth of 210 µm that is significantly higher than upon one-photon irradiation. Moreover, TPBPy localizes specifically on mitochondrion, an important organelle in cell oxidative metabolism and apoptosis. When exposed to the NIR-II irradiation, TPBPy can efficiently generate singlet oxygen ( O ) and trigger cell death. The efficacy of TPBPy-mediated 2P-PDT has also been validated using 4T1 tumor mouse model, the growth of which is significantly suppressed upon NIR-II laser irradiation. TPBPy herein serves as an excellent candidate to suppress deep tumor tissues through NIR-II 2P-PDT, and also renders a new paradigm to construct mitochondrion-anchored AIE luminogens for future cancer theranostic applications.

摘要

采用具有双光子吸收的光敏剂(PSs)的双光子光动力疗法(2P-PDT)在癌症治疗中特别引人关注,因为双光子激发能够实现精确的空间定位和深层组织穿透。在此,设计并合成了一种具有近红外(NIR)聚集诱导发光(AIE)的供体-π-受体PS(名为TPBPy)用于成像引导的2P-PDT。当TPBPy封装在脂质体中时,其最大光致发光(PL)峰高达720 nm。在近红外-II窗口(λ = 1000 nm)中用激光进行双光子照射时,TPBPy在多细胞肿瘤球体(MCTSs)模型中表现出强烈的近红外-I PL,显示出210 µm的成像深度,这明显高于单光子照射时的成像深度。此外,TPBPy特异性定位于线粒体,线粒体是细胞氧化代谢和凋亡中的重要细胞器。当暴露于近红外-II照射时,TPBPy可以有效产生活性单线态氧(O)并触发细胞死亡。TPBPy介导的2P-PDT的疗效也已在4T1肿瘤小鼠模型中得到验证,在近红外-II激光照射下,该模型的肿瘤生长受到显著抑制。本文中的TPBPy是通过近红外-II 2P-PDT抑制深部肿瘤组织的优秀候选者,并为构建用于未来癌症诊疗应用的线粒体锚定AIE发光体提供了新的范例。

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