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新型近红外磷光铱(III)配合物的合成、表征及其作为基于寿命的活细胞内 O 传感器的应用探索。

Novel NIR-Phosphorescent Ir(III) Complexes: Synthesis, Characterization and Their Exploration as Lifetime-Based O Sensors in Living Cells.

机构信息

Institute of Chemistry, Saint-Petersburg State University, Universitetskii pr., 26, 198504 St. Petersburg, Russia.

出版信息

Molecules. 2022 May 14;27(10):3156. doi: 10.3390/molecules27103156.

Abstract

A series of [Ir()()] NIR-emitting orthometalated complexes (-) has been prepared and structurally characterized using elemental analysis, mass-spectrometry, and NMR spectroscopy. The complexes display intense phosphorescence with vibrationally structured emission bands exhibiting the maxima in the range 713-722 nm. The DFT and TD DFT calculations showed that the photophysical characteristics of these complexes are largely determined by the properties of the metalating ligands, with their major contribution into formation of the lowest S and T excited states responsible for low energy absorption and emission, respectively. Emission lifetimes of in degassed methanol solution vary from 1.76 to 5.39 µs and show strong quenching with molecular oxygen to provide an order of magnitude lifetime reduction in aerated solution. The photophysics of two complexes ( and ) were studied in model physiological media containing fetal bovine serum (FBS) and Dulbecco's Modified Eagle Medium (DMEM) to give linear Stern-Volmer calibrations with substantially lower oxygen-quenching constants compared to those obtained in methanol solution. These observations were interpreted in terms of the sensors' interaction with albumin, which is an abundant component of FBS and cell media. The studied complexes displayed acceptable cytotoxicity and preferential localization, either in mitochondria () or in lysosomes () of the CHO-K1 cell line. The results of the phosphorescence lifetime imaging (PLIM) experiments demonstrated considerable variations of the sensors' lifetimes under normoxia and hypoxia conditions and indicated their applicability for semi-quantitative measurements of oxygen concentration in living cells. The complexes' emission in the NIR domain and the excitation spectrum, extending down to ca. 600 nm, also showed that they are promising for use in in vivo studies.

摘要

一系列Ir()近红外发射的正交金属配合物(-)已被制备并通过元素分析、质谱和 NMR 光谱进行了结构表征。这些配合物显示出强烈的磷光,其振动结构发射带的最大值在 713-722nm 范围内。DFT 和 TD DFT 计算表明,这些配合物的光物理特性主要取决于金属化配体的性质,它们对形成最低 S 和 T 激发态的贡献最大,分别负责低能量吸收和发射。在真空甲醇溶液中,的发射寿命从 1.76 到 5.39µs 不等,并与分子氧强烈猝灭,在充气溶液中提供一个数量级的寿命缩短。在含有胎牛血清(FBS)和 Dulbecco's Modified Eagle Medium(DMEM)的模型生理介质中研究了两个配合物(和)的光物理性质,给出了与甲醇溶液相比氧猝灭常数大大降低的线性 Stern-Volmer 校准。这些观察结果是根据传感器与白蛋白的相互作用来解释的,白蛋白是 FBS 和细胞培养基中的丰富成分。研究的配合物表现出可接受的细胞毒性和优先定位,要么在 CHO-K1 细胞系的线粒体()中,要么在溶酶体()中。磷光寿命成像(PLIM)实验的结果表明,在正常氧和缺氧条件下,传感器的寿命有很大的变化,并表明它们适用于活细胞中氧浓度的半定量测量。配合物在近红外区域的发射和激发光谱,延伸至约 600nm,也表明它们有希望用于体内研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1415/9144934/fa324b375beb/molecules-27-03156-sch001.jpg

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