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一种谷胱甘肽可激活的光动力和荧光成像单色光敏剂。

A glutathione-activatable photodynamic and fluorescent imaging monochromatic photosensitizer.

作者信息

Li Zhensheng, Liu Yang, Chen Li, Hu Xiuli, Xie Zhigang

机构信息

School of Chemistry and Chemical Engineering, Xuchang University, 88 Bayi Street, Xuchang 461000, P. R. China.

出版信息

J Mater Chem B. 2017 Jun 14;5(22):4239-4245. doi: 10.1039/c7tb00724h. Epub 2017 May 22.

Abstract

The currently available photodynamic sensitizers usually lead to undesirable side effects, including dark toxicity from heavy-atom effect and nonspecific phototoxicity. To address these issues, we designed and prepared a smart photosensitizer from boron dipyrromethene (BODIPY), and the dark toxicity and phototoxicity were reduced via heavy-atom-free substitution and controllable photosensitization, respectively. Importantly, the photodynamic effect together with fluorescence imaging can be simultaneously switched on through the suppression of intramolecular charge transfer (ICT) and photoinduced electron-transfer (PeT) induced by cancer-related biothiol glutathione (GSH) in a buffer solution. Moreover, the sensitizer exhibits obvious fluorescence enhancement and selective phototoxicity towards cancer cells in a biological system upon irradiation. The present monochromatic photosensitizer, which combines fluorescence imaging and targeted PDT treatment within a single chromophore, possesses great potentials as a new activatable theranostic reagent in cancer therapy.

摘要

目前可用的光动力敏化剂通常会导致不良副作用,包括重原子效应引起的暗毒性和非特异性光毒性。为了解决这些问题,我们设计并制备了一种基于硼二吡咯亚甲基(BODIPY)的智能光敏剂,分别通过无重原子取代和可控光致敏作用降低了暗毒性和光毒性。重要的是,在缓冲溶液中,通过抑制由癌症相关生物硫醇谷胱甘肽(GSH)诱导的分子内电荷转移(ICT)和光致电子转移(PeT),可以同时开启光动力效应和荧光成像。此外,该敏化剂在生物系统中经照射后对癌细胞表现出明显的荧光增强和选择性光毒性。这种将荧光成像和靶向光动力疗法治疗结合在单个发色团中的单色光敏剂,作为癌症治疗中一种新型的可激活治疗诊断试剂具有巨大潜力。

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