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基于谷胱甘肽转移酶的丙烯酰胺简单、选择性及快速检测

Simple, selective and fast detection of acrylamide based on glutathione -transferase.

作者信息

Bucur Madalina-Petruta, Bucur Bogdan, Radu Gabriel-Lucian

机构信息

National Institute of Research and Development for Biological Sciences, Centre of Bioanalysis 296, Splaiul Independentei 060031 Bucharest Romania

出版信息

RSC Adv. 2018 Jul 2;8(42):23931-23936. doi: 10.1039/c8ra02252f. eCollection 2018 Jun 27.

Abstract

Acrylamide (AA) is a toxic compound formed in thermally prepared foods by Maillard reaction. Besides foods, AA may be found in cosmetic products as an impurity of the widely-used non-toxic polyacrylamide. We present a novel, fast and selective detection method based on the amperometric monitoring of the coupling reaction between reduced glutathione (GSH) and AA catalyzed by glutathione -transferase (GST) to produce an electrochemically inactive compound. We have used electrodes modified with cobalt-phthalocyanine to monitor the decrease of GHS concentration at +300 mV. Our system is simple, does not require supplementary substrates such as 1-chloro-2,4-dinitrobenzene (CDNB) nor have disadvantageous competitive kinetics characteristic to inhibition like signals. Using the optimum concentration of 100 μM GSH we have obtained a linear calibration graph from 7 to 50 μM AA and a limit of detection of 5 μM AA. The method is not affected by interfering compounds usually found in foods and was applied for real sample analysis.

摘要

丙烯酰胺(AA)是热加工食品中通过美拉德反应形成的一种有毒化合物。除食品外,AA还可能作为广泛使用的无毒聚丙烯酰胺的杂质存在于化妆品中。我们提出了一种基于安培法监测还原型谷胱甘肽(GSH)与AA在谷胱甘肽转移酶(GST)催化下的偶联反应以产生电化学惰性化合物的新型、快速且选择性的检测方法。我们使用了钴酞菁修饰的电极来监测在 +300 mV 时 GSH 浓度的降低。我们的系统简单,不需要诸如 1 - 氯 - 2,4 - 二硝基苯(CDNB)等补充底物,也没有像信号抑制那样不利的竞争动力学特征。使用 100 μM GSH 的最佳浓度,我们得到了 7 至 50 μM AA 的线性校准曲线以及 5 μM AA 的检测限。该方法不受食品中常见干扰化合物的影响,并应用于实际样品分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c89/9081860/c9e1a63f8e51/c8ra02252f-f1.jpg

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