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Glutathione dimerization-based plasmonic nanoswitch for biodetection of reactive oxygen and nitrogen species

机译:基于谷胱甘肽二聚化的等离激元纳米开关用于生物活性氧和氮的检测

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摘要

Reactive oxygen and nitrogen species (ROS and RNS) are continuously produced in the cellular systems and are controlled by several antioxidant mechanisms. Here, we developed a straightforward, sensitive, and quantitative assay for the colorimetric and spectroscopic detection of various ROS and RNS such as H_2O_2, ·OH, ~-OCl, NO·, and O_2 ~- using glutathione-modified gold nanoparticles (GSH-AuNPs). A basic principle here is that the GSHs on the AuNP surface can be readily detached via the formation of glutathione disulfides upon the addition of ROS and RNS, and destabilized particles can aggregate to generate the plasmonic couplings between plasmonic AuNPs that trigger the red shift in UV-vis spectrum and solution color change. For nonradical species such as H _2O_2, this process can be more efficiently achieved by converting them into radical species via the Fenton reaction. Using this strategy, we were able to rapidly and quantitatively distinguish among cancerous and normal cells based on ROS and RNS production.
机译:活性氧和氮物质(ROS和RNS)在细胞系统中连续产生,并受多种抗氧化剂机制控制。在这里,我们开发了一种简单,灵敏和定量的测定方法,用于使用谷胱甘肽修饰的金纳米粒子(GSH-)对比色法和光谱法检测各种ROS和RNS(例如H_2O_2,·OH,〜-OCl,NO·和O_2〜-)。 AuNPs)。此处的基本原理是,在加入ROS和RNS时,通过形成谷胱甘肽二硫化物可以很容易地分离AuNP表面的GSH,并且不稳定的颗粒可以聚集在一起,从而在等离子AuNP之间产生等离子耦合,从而触发UV的红移。 -可见光谱和溶液颜色变化。对于非自由基物质,例如H _2O_2,可以通过Fenton反应将其转化为自由基,从而更有效地实现此过程。使用这种策略,我们能够根据ROS和RNS的产生快速定量地区分癌细胞和正常细胞。

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