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使用硫醇-二硫化物交换剂二硫苏糖醇测定生物样品中的谷胱甘肽二硫化物水平。

Determination of glutathione disulfide levels in biological samples using thiol-disulfide exchanging agent, dithiothreitol.

作者信息

Ates Burhan, Ercal Baris Can, Manda Kalyan, Abraham Linu, Ercal Nuran

机构信息

Department of Chemistry, Missouri University of Science and Technology, 400 West 11th Street, Rolla, MO 65409, USA.

出版信息

Biomed Chromatogr. 2009 Feb;23(2):119-23. doi: 10.1002/bmc.1083.

Abstract

A reverse-phase HPLC method incorporating dithiothreitol (DTT) reduction for quantitative determination of oxidized glutathione (GSSG) in biological samples is described here. This method is based on our previous enzymatic reduction technique that uses N-1-(pyrenyl) maleimide (NPM) as a derivatizing agent. In our earlier method, glutathione disulfide (GSSG) was measured by first reducing it to GSH with glutathione reductase (GR) in the presence of NADPH. However, this is a very costly and time-consuming technique. The method described here employs a common and inexpensive thiol-disulfide exchanging agent, DTT, for reduction of GSSG to GSH, followed by derivatization with NPM. The calibration curves are linear over a concentration range of 25-1250 nm (r(2) > 0.995). The coefficients of variations for intra-run precision and inter-run precision range from 0.49 to 5.10% with an accuracy range of 1.78-6.15%. The percentage of relative recovery ranges from 97.3 to 103.2%. This new method provides a simple, efficient, and cost-effective way of determining glutathione disulfide levels with a 2.5 nm limit of detection per 5 microL injection volume.

摘要

本文介绍了一种结合二硫苏糖醇(DTT)还原法的反相高效液相色谱法,用于定量测定生物样品中的氧化型谷胱甘肽(GSSG)。该方法基于我们之前的酶促还原技术,该技术使用N-1-(芘基)马来酰亚胺(NPM)作为衍生剂。在我们早期的方法中,首先在NADPH存在下用谷胱甘肽还原酶(GR)将谷胱甘肽二硫化物(GSSG)还原为GSH,然后进行测定。然而,这是一种非常昂贵且耗时的技术。本文所述方法采用一种常见且廉价的硫醇-二硫化物交换剂DTT,将GSSG还原为GSH,然后用NPM进行衍生化。校准曲线在25 - 1250 nM的浓度范围内呈线性(r(2) > 0.995)。批内精密度和批间精密度的变异系数范围为0.49%至5.10%,准确度范围为1.78%至6.15%。相对回收率范围为97.3%至103.2%。这种新方法提供了一种简单、高效且经济高效的方法来测定谷胱甘肽二硫化物水平,每5 μL进样体积的检测限为2.5 nM。

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