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钌(II)-芳基姜黄素配合物作为抗肿瘤和抗菌光动力治疗的光敏剂:体外和体内研究进展。

Ruthenium(II)-Arene Curcuminoid Complexes as Photosensitizer Agents for Antineoplastic and Antimicrobial Photodynamic Therapy: In Vitro and In Vivo Insights.

机构信息

Department of Biotechnology and Life Sciences (DBSV), University of Insubria, Via JH Dunant 3, 21100 Varese, Italy.

Department of Theoretical and Applied Sciences (DiSTA), University of Insubria, Via JH Dunant 3, 21100 Varese, Italy.

出版信息

Molecules. 2023 Nov 11;28(22):7537. doi: 10.3390/molecules28227537.

Abstract

Photodynamic therapy (PDT) is an anticancer/antibacterial strategy in which photosensitizers (PSs), light, and molecular oxygen generate reactive oxygen species and induce cell death. PDT presents greater selectivity towards tumor cells than conventional chemotherapy; however, PSs have limitations that have prompted the search for new molecules featuring more favorable chemical-physical characteristics. Curcumin and its derivatives have been used in PDT. However, low water solubility, rapid metabolism, interference with other drugs, and low stability limit curcumin use. Chemical modifications have been proposed to improve curcumin activity, and metal-based PSs, especially ruthenium(II) complexes, have attracted considerable attention. This study aimed to characterize six Ru(II)-arene curcuminoids for anticancer and/or antibacterial PDT. The hydrophilicity, photodegradation rates, and singlet oxygen generation of the compounds were evaluated. The photodynamic effects on human colorectal cancer cell lines were also assessed, along with the ability of the compounds to induce ROS production, apoptotic, necrotic, and/or autophagic cell death. Overall, our encouraging results indicate that the Ru(II)-arene curcuminoid derivatives are worthy of further investigation and could represent an interesting option for cancer PDT. Additionally, the lack of significant in vivo toxicity on the larvae of is an important finding. Finally, the photoantimicrobial activity of against Gram-positive bacteria is indeed promising.

摘要

光动力疗法(PDT)是一种抗癌/抗菌策略,其中光敏剂(PSs)、光和分子氧产生活性氧物种并诱导细胞死亡。PDT 对肿瘤细胞的选择性高于传统化疗;然而,PSs 存在一些限制,这促使人们寻找具有更有利的理化特性的新分子。姜黄素及其衍生物已用于 PDT。然而,低水溶性、快速代谢、与其他药物的干扰以及低稳定性限制了姜黄素的使用。已经提出了化学修饰来提高姜黄素的活性,并且基于金属的 PSs,特别是钌(II)配合物,引起了相当大的关注。本研究旨在表征六种 Ru(II)-芳基姜黄素类化合物用于抗癌和/或抗菌 PDT。评估了化合物的亲水性、光降解速率和单线态氧生成。还评估了化合物对人结肠癌细胞系的光动力作用,以及诱导 ROS 产生、凋亡、坏死和/或自噬细胞死亡的能力。总的来说,我们令人鼓舞的结果表明,Ru(II)-芳基姜黄素衍生物值得进一步研究,可能是癌症 PDT 的一个有趣选择。此外,在 幼虫中缺乏明显的体内毒性是一个重要发现。最后, 对革兰氏阳性菌的光抗菌活性确实很有前途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a86f/10673066/1e2af7196f1e/molecules-28-07537-g001.jpg

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