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用于药物性肝损伤模型中检测过氧亚硝酸盐波动的双靶标荧光探针。

Dual-targetable fluorescent probe for mapping the fluctuation of peroxynitrite in drug-induced liver injury model.

机构信息

Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province and State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China; Laboratory for Nanomedical Photonics, School of Basic Medical Science, Henan University, Kaifeng 475004, PR China.

Laboratory for Nanomedical Photonics, School of Basic Medical Science, Henan University, Kaifeng 475004, PR China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2023 Feb 5;286:121892. doi: 10.1016/j.saa.2022.121892. Epub 2022 Sep 17.

Abstract

Drug-induced liver injury (DILI) is one of the most common and serious adverse drug reactions which can cause acute liver failure or even death in severe cases. With the incidence rate increasing over the years, DILI has became a frequent clinical liver disease and a global public health problem. As a biomarker of DILI, the detection of peroxynitrite (ONOO) has became a powerful tool for the early diagnosis of liver injury. Here, we synthesized five mitochondria-targetable probes, 1-5, for detecting endogenous ONOO. Through dye-screening, probe 5 was stood out by its excellent performance. In the presence of ONOO, the fluorescence signal of probe 5 reduced 40-fold in 19 s with a low detection limit (9.36 nM). At the same time, the transformation can be observed with the naked eye under sunlight or UV lamp without being affected by the other reactive species. Even better, with low toxicity and high biocompatibility, probe 5 could successfully detect endogenous ONOO in the mitochondrion of cells. Finally, probe 5 could specifically target the liver, and can be employed for monitoring the therapeutic effect of hepatoprotective medicine after drug-induced hepatotoxicity in vivo. In brief, probe 5 has the practical application capability for diagnosing the severity of the liver injury and researching the therapeutic effect of antidote in complex bio-systems.

摘要

药物性肝损伤(DILI)是最常见和最严重的药物不良反应之一,在严重的情况下可导致急性肝衰竭甚至死亡。随着近年来发病率的上升,DILI 已成为一种常见的临床肝病和全球公共卫生问题。过氧亚硝酸盐(ONOO)作为 DILI 的生物标志物,其检测已成为肝损伤早期诊断的有力工具。在这里,我们合成了 5 种线粒体靶向探针 1-5 来检测内源性 ONOO。通过染料筛选,探针 5 因其优异的性能脱颖而出。在 ONOO 的存在下,探针 5 的荧光信号在 19 秒内减少了 40 倍,检测限低至 9.36 nM。同时,在阳光或紫外灯下无需受其他活性物质的影响,即可用肉眼观察到这种转变。更好的是,探针 5 具有低毒性和高生物相容性,可成功检测细胞线粒体中的内源性 ONOO。最后,探针 5 可以特异性靶向肝脏,并可用于监测体内药物性肝毒性后肝保护药物的治疗效果。总之,探针 5 具有在复杂生物体系中诊断肝损伤严重程度和研究解毒剂治疗效果的实际应用能力。

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