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两种基于罗丹明偶氮的荧光探针用于识别三价金属离子:晶体结构阐明和生物应用。

Two rhodamine-azo based fluorescent probes for recognition of trivalent metal ions: crystal structure elucidation and biological applications.

机构信息

Department of Chemistry, Jadavpur University, Kolkata-700032, India.

Department of Life Science and Biotechnology, Jadavpur University, Kolkata-700032, India.

出版信息

Dalton Trans. 2022 Oct 18;51(40):15555-15570. doi: 10.1039/d2dt00399f.

Abstract

Two rhodamine and azo based chemosensors (HL1 = (3',6'-bis(ethylamino)-2-((2-hydroxy-3-methoxy-5-(phenyldiazenyl)benzylidene)amino)-2',7'-dimethylspiro[isoindoline-1,9'-xanthen]-3-one) and HL2 = (3',6'-bis(ethylamino)-2-(((2-hydroxy-3-methoxy-5-(-tolyldiazenyl)benzylidene)amino)-2',7'-dimethylspiro[isoindoline-1,9'-xanthen]-3-one) have been synthesized for colorimetric and fluorometric detection of three trivalent metal ions, Al, Cr and Fe. The chemosensors have been thoroughly characterized by different spectroscopic techniques and X-ray crystallography. They are non-fluorescent due to the presence of a spirolactam ring. The trivalent metal ions initiate an opening of the spirolactam ring when excited at 490 nm in Britton-Robinson buffer solution (HO/MeOH 1 : 9 v/v; pH 7.4). The opening of the spirolactam ring increases conjugation within the probe, which is supported by an intense fluorescent pinkish-yellow colouration and an enhancement of the fluorescence intensity of the chemosensors by ∼400 times in the presence of Al and Cr ions and by ∼100 times in the presence of Fe ions. Such a type of enormous fluorescence enhancement is rarely observed in other chemosensors for the detection of trivalent metal ions. A 2 : 1 binding stoichiometry of the probes with the respective ions has been confirmed by Job's plot analysis. Elucidation of the crystal structures of the Al bound chemosensors (1 and 4) also justifies the 2 : 1 binding stoichiometry and the presence of an open spirolactam ring within the chemosensor framework. The limit of detection (LOD) values for both the chemosensors towards the respective metal ions are in the order of ∼10 M which supports their application in the biological field. The biocompatibility of the ligands has been studied with the help of the MTT assay. The results show that no significant toxicity was observed up to 100 μM of chemosensor concentration. The capability of our synthesized chemosensors to detect intracellular Al, Cr and Fe ions in the cervical cancer cell line HeLa was evaluated with the aid of fluorescence imaging.

摘要

两种基于若丹明和偶氮的化学传感器(HL1=(3',6'-双(乙基氨基)-2-((2-羟基-3-甲氧基-5-(苯基亚氨基)亚苄基)氨基)-2',7'-二甲基螺[异吲哚啉-1,9'-氧杂蒽]-3-酮)和 HL2=(3',6'-双(乙基氨基)-2-((2-羟基-3-甲氧基-5-(-甲苯基亚氨基)亚苄基)氨基)-2',7'-二甲基螺[异吲哚啉-1,9'-氧杂蒽]-3-酮)已被合成用于三价金属离子 Al、Cr 和 Fe 的比色和荧光检测。化学传感器已经通过不同的光谱技术和 X 射线晶体学进行了彻底的表征。由于螺内酯环的存在,它们没有荧光。当在 Britton-Robinson 缓冲溶液(HO/MeOH 1:9 v/v;pH 7.4)中在 490nm 处激发时,三价金属离子会引发螺内酯环的打开。螺内酯环的打开增加了探针内的共轭,这得到了强烈的粉红色-黄色荧光着色和化学传感器荧光强度增强约 400 倍的支持,在存在 Al 和 Cr 离子的情况下,以及在存在 Fe 离子的情况下增强约 100 倍。在其他用于检测三价金属离子的化学传感器中很少观察到这种类型的巨大荧光增强。通过 Job 图分析证实了探针与相应离子的 2:1 结合化学计量比。对 Al 结合化学传感器(1 和 4)晶体结构的阐明也证明了 2:1 的结合化学计量比和化学传感器框架内存在开环螺内酯环。两种化学传感器对各自金属离子的检测限(LOD)值均在约 10 M 的范围内,支持其在生物领域的应用。借助 MTT 测定法研究了配体的生物相容性。结果表明,在高达 100 μM 的化学传感器浓度下,没有观察到明显的毒性。利用荧光成像评估了我们合成的化学传感器在宫颈癌 HeLa 细胞系中检测细胞内 Al、Cr 和 Fe 离子的能力。

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