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一种高荧光且易于获取的全有机光敏剂模型,可用于推进图像引导的癌症 PDT。

A highly fluorescent and readily accessible all-organic photosensitizer model for advancing image-guided cancer PDT.

机构信息

Institute for Liver and Digestive Health, Royal Free Hospital Campus, University College London, Pond Street, London NW3 2QG, UK.

Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, 28040 Madrid, Spain.

出版信息

J Mater Chem B. 2024 Aug 7;12(31):7618-7625. doi: 10.1039/d4tb00385c.

Abstract

The potential of using image-guided photodynamic therapy (ig-PDT) for cancer, especially with highly biocompatible fluorescent agents free of heavy atoms, is well recognized. This is due to key advantages related to minimizing adverse side effects associated with standard cancer chemotherapy. However, this theragnostic approach is strongly limited by the lack of synthetically-accessible and easily-modulable chemical scaffolds, enabling the rapid design and construction of advanced agents for clinical ig-PDT. In fact, there are still very few ig-PDT agents clinically approved. Herein we report a readily accessible, easy-tunable and highly fluorescent all-organic small photosensitizer, as a model design for accelerating the development and translation of advanced ig-PDT agents for cancer. This scaffold is based on BODIPY, which assures high fluorescence, accessibility, and ease of performance adaptation by workable chemistry. The optimal PDT performance of this BODIPY dye, tested in highly resistant pancreatic cancer cells, despite its high fluorescent behavior, maintained even after fixation and cancer cell death, is based on its selective accumulation in mitochondria. This induces apoptosis upon illumination, as evidenced by proteomic studies and flow cytometry. All these characteristics make the reported BODIPY-based fluorescent photosensitizer a valuable model for the rapid development of ig-PDT agents for clinical use.

摘要

利用图像引导的光动力疗法(ig-PDT)治疗癌症的潜力,特别是使用高度生物相容的不含重金属原子的荧光剂,已经得到了广泛的认可。这是因为与标准癌症化疗相关的不良反应最小化具有关键优势。然而,这种治疗方法受到缺乏可合成且易于修饰的化学支架的强烈限制,这限制了用于临床 ig-PDT 的先进试剂的快速设计和构建。事实上,临床上批准的 ig-PDT 试剂仍然很少。在这里,我们报告了一种易于获得、易于调节且具有高荧光的全有机小分子光敏剂,作为加速开发和转化用于癌症的先进 ig-PDT 试剂的模型设计。该支架基于 BODIPY,通过可行的化学方法确保了高荧光性、可及性和性能适应性的容易调节。该 BODIPY 染料在高度耐药的胰腺癌细胞中的最佳 PDT 性能,尽管其荧光强度很高,但在固定和癌细胞死亡后仍能保持,这是基于其在线粒体中的选择性积累。这会在光照下诱导细胞凋亡,这一点可以通过蛋白质组学研究和流式细胞术来证明。所有这些特性使所报道的基于 BODIPY 的荧光光敏剂成为用于临床的 ig-PDT 试剂快速开发的有价值的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d08/11305095/165bcd4b9967/d4tb00385c-f1.jpg

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