介-取代的 AB3 型吩噻嗪基卟啉及其铟和锌配合物对卵巢癌细胞的光敏特性、细胞毒性和光毒性。

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Brém Balázs, Bianca Stoean Vasile, Éva Molnár, Eva Fischer-Fodor, Ovidiu Bălăcescu, Raluca Borlan, Monica Focsan, Adriana Grozav, Patriciu Achimaş-Cadariu, Emese Gál, Luiza Gaina
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引用次数: 0

摘要

通过 Suzuki-Miyaura 和 Mizoroki-Heck 交叉偶联反应,分别合成了新的中取代 AB3 型吩噻嗪基卟啉和二茂铁乙烯基吩噻嗪基卟啉。游离卟啉被进一步用于合成新的铟(iii)或锌(ii)卟啉络合物。所有卟啉在溶液中都会发出红色荧光,荧光显微镜图像显示,这种特性在卵巢 A2780 癌细胞内化后依然保持不变。与游离基卟啉前体或 Zn(ii) 复合物 4b 相比,In(iii) 吩噻嗪基卟啉复合物的荧光发射量子产率更高(2aΦ F = 30%、4aΦ F = 29%、5aΦ F = 28%)(Φ F = 10%)。新型吩噻嗪基卟啉作为光敏剂的潜力通过两种不同的方法进行了评估。第一种方法是测量单线态氧量子产率 Φ Δ(1O2),第二种方法是在黑暗和光照条件下体外测量代谢活性、氧化应激、核因子-红细胞 2 相关因子 2 (Nrf-2)激活和肿瘤坏死因子-α (TNF-α)。从 IC50 值来看,In(iii) ferrocenylvinyl phenothiazinyl porphyrin 4a 对 A2780 细胞的细胞毒性最强(36.38 μM),其余化合物的细胞毒性较弱。与无光处理相比,用 4a 和 6a 处理并暴露在光下的 A2780 卵巢肿瘤细胞的代谢活性降低。在用 4a 处理 A2780 细胞并随后进行光照射时,氧化应激、TNF-α 和 Nrf-2 转录因子的作用尤为显著,氧化应激与 4a 记录的最高 Φ Δ(1O2)值(60%)有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
meso-Substituted AB3-type phenothiazinyl porphyrins and their indium and zinc complexes photosensitising properties, cytotoxicity and phototoxicity on ovarian cancer cells.

New meso-substituted AB3-type phenothiazinyl porphyrins and ferrocenylvinyl phenothiazinyl porphyrin were synthesised by Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions, respectively. The free porphyrins were further used in the synthesis of new indium(iii) or zinc(ii) porphyrin complexes. All porphyrins exhibit red fluorescence emission in solution, a property that remains unimpaired following internalisation in ovarian A2780 cancer cells, as evidenced by fluorescence microscopy images. The In(iii) phenothiazinyl porphyrin complexes show a higher quantum yield of fluorescence emission (2aΦ F = 30%, 4aΦ F = 29%, 5aΦ F = 28%) compared to the free base porphyrin precursors, or Zn(ii) complex 4b (Φ F = 10%). The potential of novel phenothiazinyl porphyrins to act as photosensitisers was evaluated using two distinct approaches. The first was through the measurement of the singlet oxygen quantum yield Φ Δ(1O2), while the second employed in vitro measurements of metabolic activity, oxidative stress, nuclear factor-erythroid 2 related factor 2 (Nrf-2) activation and tumour necrosis factor-alpha (TNF-α) under both dark and light irradiation conditions. As reflected by the IC50 values, the most potent cytotoxicity of the phenothiazinyl porphyrins against the A2780 cells was observed for In(iii) ferrocenylvinyl phenothiazinyl porphyrin 4a (36.38 μM), the remaining compounds are less cytotoxic. The reduction in metabolic activity was observed in A2780 ovarian tumour cells treated with 4a and 6a and exposed to light compared to treatment in the absence of light. The oxidative stress, TNF-α and Nrf-2 transcription factor were particularly notable when A2780 cells were treated with 4a and subsequently photoirradiated, the oxidative stress was linked to the highest value of Φ Δ(1O2) recorded for 4a (60%).

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