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Cucurbit[8]uril Regulated Activatable Supramolecular Photosensitizer for Targeted Cancer Imaging and Photodynamic Therapy

机译:葫芦[8]尿素调控的可活化超分子光敏剂,用于靶向癌症的成像和光动力疗法

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摘要

Activatable photosensitizers (aPSs) have emerged as promising photodynamic therapy (PDT) agents for simultaneous imaging and selective ablation of cancer. However, traditional synthetic aPSs are limited by complex design and tedious synthesis. Here, aPS regulated by cucurbit[8]uril (CB[8]) for targeted cancer imaging and PDT is reported. This system is based on the host guest interaction between biotinylated toluidine blue (TB-B) and CB[8] to form 2TB-B@CB [8]. Moreover, a facile strategy to turn off/on the fluorescence and photodynamic activity of TB B is developed through the reversible assembly/disassembly of 2TB-B@CB [8]. This established system can achieve selective accumulation in tumor, light-up cancer imaging, and enhanced anticancer behavior. Therefore, this work provides a novel and promising strategy for the aPS build via simple and facile regulation of supramolecular chemistry.
机译:可激活的光敏剂(aPSs)已成为有前途的光动力疗法(PDT)剂,用于同时成像和选择性消融癌症。但是,传统的合成aPS受复杂的设计和繁琐的合成限制。在这里,据报道葫芦[8]尿素(CB [8])调节的aPS用于靶向癌症成像和PDT。该系统基于生物素化甲苯胺蓝(TB-B)和CB [8]之间形成2TB-B @ CB的宿主客体相互作用[8]。此外,通过2TB-B @ CB的可逆组装/拆卸,开发了一种简便的策略来关闭/打开TB B的荧光和光动力活性[8]。这个已建立的系统可以在肿瘤中选择性积累,照亮癌症成像并增强抗癌行为。因此,这项工作通过对超分子化学的简单而轻松的调节,为aPS构建提供了一种新颖而有希望的策略。

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