吖啶二酮-邻苯二甲酰亚胺共轭物:用于光学和光动力疗法的分子内电子转移和单线态氧生成研究。

IF 2.7 3区 化学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Photochemical & Photobiological Sciences Pub Date : 2024-08-01 Epub Date: 2024-06-27 DOI:10.1007/s43630-024-00603-9
Mohamed E El-Khouly, Hassan A Khatab, Ayamn A Abdel-Shafi, Sherif F Hammad
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引用次数: 0

摘要

我们在此报告了用于光学和医学应用的邻苯二甲酰亚胺(Phth)和吖啶-1,8-二酮(Acr)混合共轭物的合成和表征。合成过程采用了三步合成策略。利用各种光谱技术,如稳态吸收、荧光和时间相关单光子计数等,考察了 1,8-吖啶二酮-邻苯二甲酰亚胺连接分子(AcrPhth 1-5)的光学特性。稳态吸收研究表明,AcrPhth 1-5 可吸收紫外线和可见光区域的光。与吖啶二酮对照化合物(Acr 1-5)相比,AcrPhth 1-5 的荧光研究显示出明显的荧光淬灭现象,这表明从电子捐赠的吖啶二酮分子(Acr)到电子接受的邻苯二甲酰亚胺分子(Phth)之间发生了电子转移反应。通过荧光寿命测量确定了电子转移反应的速率和效率,表明共价连接的 AcrPhth 1-5 共轭物具有快速的电子转移过程。利用 ab initio B3LYP/6-311G 方法进行的计算研究支持了 AcrPhth 共轭物的分子内电子转移反应。在优化结构中,发现 HOMO 完全位于 Acr 实体上,而 LUMO 则完全位于 Phth 实体上。此外,合成的化合物还被测试用作产生单线态氧的光敏剂,单线态氧是光动力疗法(PDT)应用中的一个关键因素。通过纳秒激光闪烁测量,我们可以检测到所研究的 Acr 和 AcrPhth 共轭物的三重激发态,确定三重量子产率,并直接准确地检测到单线态氧。通过观察发现,单线量子产率在 0.12-0.27 (Acr 1-5)和 0.07-0.19 (AcrPhth 1-5 共轭物)之间。分子对接研究显示,化合物 AcrPhth 2 与关键基因(p53、TOP2B、p38 和表皮生长因子受体)具有很高的结合亲和力,这表明它具有靶向抗癌疗法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Acridinedione-phthalimide conjugates: Intramolecular electron transfer and singlet oxygen generation studies for optical and photodynamic therapy applications.

We reported herein the synthesis, characterization of hybrid conjugates composed of phthalimide (Phth) and acridine-1,8-diones (Acr) for optical and medical applications. For the synthetic procedure, a three-step synthetic strategy has been utilized. The optical properties of the examined 1,8-acridinedione-phthalimide connected molecules (AcrPhth 1-5) have been examined utilizing various spectroscopic techniques, e.g., steady-state absorption and fluorescence, and time-correlated single photon counting. The steady-state absorption studies showed that AcrPhth 1-5 absorbs the light in the UV and visible region. The fluorescence studies of AcrPhth 1-5 exhibited significant fluorescence quenching compared to the acridinedione control compounds (Acr 1-5) suggesting the occurrence of electron-transfer reactions from the electron donating acridinedione moiety (Acr) to the electron accepting phthalimide moiety (Phth). The rate and efficiency of the electron-transfer reactions were determined from the fluorescence lifetime measurements indicating the fast electron-transfer processes of the covalently connected AcrPhth 1-5 conjugates. Computational studies supported the intramolecular electron-transfer reaction of AcrPhth conjugates using ab initio B3LYP/6-311G methods. In the optimized structures, the HOMO was found to be entirely located on the Acr entity, while the LUMO was found to be entirely on the Phth entity. Further, the synthesized compounds were tested as photosensitizers for generating the singlet oxygen species, which is a key factor in the photodynamic therapy (PDT) applications. The nanosecond laser flash measurements enable us to detect the triplet-excited states of examined Acr and AcrPhth conjugates, determining the triplet quantum yields, and direct detecting the singlet oxygen in an accurate way. From this observation, the singlet quantum yields were found to be in the range of 0.12-0.27 (for Acr 1-5) and 0.07-0.19 (for AcrPhth 1-5 conjugates). The molecular docking studies revealed that compound AcrPhth 2 exhibited high binding affinity with for key genes (p53, TOP2B, p38, and EGFR) suggesting its potential as a targeted anticancer therapy.

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来源期刊
Photochemical & Photobiological Sciences
Photochemical & Photobiological Sciences 生物-生化与分子生物学
CiteScore
5.60
自引率
6.50%
发文量
201
审稿时长
2.3 months
期刊介绍: A society-owned journal publishing high quality research on all aspects of photochemistry and photobiology.
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