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一种对一氧化碳有响应的咪唑功能化荧光材料介导癌症化疗。

A CO-Responsive Imidazole-Functionalized Fluorescent Material Mediates Cancer Chemotherapy.

作者信息

Ngan Vo Thuy Thien, Chiou Po-Yen, Ilhami Fasih Bintang, Bayle Enyew Alemayehu, Shieh Yeong-Tarng, Chuang Wei-Tsung, Chen Jem-Kun, Lai Juin-Yih, Cheng Chih-Chia

机构信息

Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 10607, Taiwan.

Department of Chemical and Materials Engineering, National University of Kaohsiung, Kaohsiung 81148, Taiwan.

出版信息

Pharmaceutics. 2023 Jan 20;15(2):354. doi: 10.3390/pharmaceutics15020354.

Abstract

We present a breakthrough in the synthesis and development of functional gas-responsive materials as highly potent anticancer agents suitable for applications in cancer treatment. Herein, we successfully synthesised a stimuli-responsive multifunctional material (I-R6G) consisting of a carbon dioxide (CO)-sensitive imidazole moiety and spirolactam-containing conjugated rhodamine 6G (R6G) molecule. The resulting I-R6G is highly hydrophobic and non- or weakly fluorescent. Simple CO bubbling treatment induces hydrophobic I-R6G to completely dissolve in water and subsequently form self-assembled nanoparticles, which exhibit unique optical absorption and fluorescence behaviours in water and extremely low haemolytic ability against sheep red blood cells. Reversibility testing indicated that I-R6G undergoes reversible CO/nitrogen (N)-dependent stimulation in water, as its structural and physical properties can be reversibly and stably switched by alternating cycles of CO and N bubbling. Importantly, in vitro cellular assays clearly demonstrated that the CO-protonated imidazole moiety promotes rapid internalisation of CO-treated I-R6G into cancer cells, which subsequently induces massive levels of necrotic cell death. In contrast, CO-treated I-R6G was not internalised and did not affect the viability of normal cells. Therefore, this newly created system may provide an innovative and efficient route to remarkably improve the selectivity, safety and efficacy of cancer treatment.

摘要

我们展示了功能性气体响应材料在合成与开发方面的一项突破,该材料可作为高效抗癌剂,适用于癌症治疗。在此,我们成功合成了一种刺激响应性多功能材料(I-R6G),它由对二氧化碳(CO₂)敏感的咪唑部分和含螺内酰胺的共轭罗丹明6G(R6G)分子组成。所得的I-R6G具有高度疏水性,无荧光或荧光较弱。简单的CO₂鼓泡处理可使疏水性的I-R6G完全溶解于水中,并随后形成自组装纳米颗粒,这些纳米颗粒在水中表现出独特的光吸收和荧光行为,且对绵羊红细胞的溶血能力极低。可逆性测试表明,I-R6G在水中会经历可逆的CO₂/氮气(N₂)依赖性刺激,因为其结构和物理性质可通过交替进行CO₂和N₂鼓泡循环而可逆且稳定地切换。重要的是,体外细胞实验清楚地表明,CO₂质子化的咪唑部分促进了经CO₂处理的I-R6G快速内化进入癌细胞,随后诱导大量细胞坏死死亡。相比之下,经CO₂处理的I-R6G不会被正常细胞内化,也不会影响其活力。因此,这个新创建的系统可能为显著提高癌症治疗的选择性、安全性和疗效提供一条创新且高效的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a59/9959563/6631d613b887/pharmaceutics-15-00354-sch001.jpg

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