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基于硼二吡咯-铜配合物的一氧化氮可激活光动力治疗剂

Nitric Oxide Activatable Photodynamic Therapy Agents Based on BODIPY-Copper Complexes.

作者信息

Ilhan Huriye, Şeker Merve, Gülseren Gülcihan, Bakırcı Melike Ebrar, Boyacı Ayşe İlayda, Cakmak Yusuf

机构信息

Department of Biotechnology, Graduate School of Natural & Applied Sciences, Konya Food and Agriculture University, 42080 Konya, Turkey.

Department of Metallurgical and Materials Engineering & Science and Technology Research and Application Center (BITAM), Necmettin Erbakan University, 42090 Konya, Turkey.

出版信息

ACS Pharmacol Transl Sci. 2024 Dec 10;8(3):679-689. doi: 10.1021/acsptsci.4c00428. eCollection 2025 Mar 14.

Abstract

In this work, two BODIPY-bipyridine Cu ion complexes for targeted nitric oxide (NO) activatable photodynamic therapy are reported. The design is based on the relatively high concentration of these small gas molecules in the tumor microenvironment. Copper(II) ion complexation to the photosensitizer renders it in the OFF position in terms of fluorescence and reactive oxygen species (ROS) production. The interaction of the Cu-BODIPY complex with nitric oxide interchanges both fluorescence and therapy mode into the ON state through the detachment of the cation. Therefore, targeting the cancer cells would be expected to be achieved in this way. Moreover, one of the compounds, , has increased aqueous solubility due to the polar structure. The designed structures also have near-infrared (IR) absorption ability up to 800 nm aqueous solutions. In addition, through using in vitro cell culture studies with HeLa and RAW264.7 cell lines, we confirmed that and could be activated in the presence of NO, and cell photocytotoxicity occurred extensively compared with the NO-absent cells. We believe that this work will provide new opportunities for the increased efficacy of the photodynamic treatment of cancer and smart photosensitizer design.

摘要

在这项工作中,报道了两种用于靶向一氧化氮(NO)可激活光动力疗法的BODIPY-联吡啶铜离子配合物。该设计基于肿瘤微环境中这些小分子气体的相对高浓度。铜(II)离子与光敏剂络合使其在荧光和活性氧(ROS)产生方面处于关闭状态。Cu-BODIPY配合物与一氧化氮的相互作用通过阳离子的脱离将荧光和治疗模式都转换为开启状态。因此,预计通过这种方式可以实现对癌细胞的靶向。此外,其中一种化合物,由于其极性结构而具有增加的水溶性。所设计的结构在高达800 nm的水溶液中也具有近红外(IR)吸收能力。此外,通过使用HeLa和RAW264.7细胞系进行体外细胞培养研究,我们证实了在有NO的情况下 和 可以被激活,并且与无NO的细胞相比,细胞光细胞毒性广泛发生。我们相信这项工作将为提高癌症光动力治疗的疗效和智能光敏剂设计提供新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f86f/11915034/1d6e7e9c520a/pt4c00428_0001.jpg

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