首页> 外文期刊>Analytical and bioanalytical chemistry >Field-amplified sample injection combined with pressure-assisted capillary electrophoresis UV detection for the simultaneous analysis of allantoin, uric acid, and malondialdehyde in human plasma
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Field-amplified sample injection combined with pressure-assisted capillary electrophoresis UV detection for the simultaneous analysis of allantoin, uric acid, and malondialdehyde in human plasma

机译:现场放大样品注射结合压力辅助毛细管电泳UV检测可同时分析人血浆中的尿囊素,尿酸和丙二醛

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摘要

The allantoin/uric acid (All/UA) ratio and malondialdehyde (MDA) plasma levels have been proposed as important markers for monitoring oxidation triggered by the action of free radicals (FR). Here, we describe an easy field amplified sample injection capillary electrophoresis method with UV detection for the separation and quantification of All, UA, and free MDA in human plasma. The plasma samples were simply filtered through centrifugation membrane tubes for protein elimination and directly injected on a capillary without complex cleanup and/or sample derivatization procedures. The use of a run buffer composed of 300?mmol/L sodium borate at pH 10 with 50?mmol/L of N-methyl-d-glucamine and an overimposed pressure/voltage of 0.1?psi during the electrophoretic run allows basline resolution of the analytes within 17?min. The electrokinetic injection allows a detection limit of 15?nmol/L for All, 20?nmol/L for UA and 10?nmol/L for MDA in a plasma sample, thus significantly improving the LOD of previous described methods based on capillary electrophoresis. Precision tests indicate a good repeatability of our method both for migration times (CV?=?1.85%) and areas (CV?=?2.87%). Moreover, a good reproducibility of intra- and inter-assay tests was obtained (CV?=?4.63% and CV?=?6.59% respectively). The suitability of the method was tested by measuring analyte levels in 40 healthy volunteers.
机译:尿囊素/尿酸(All / UA)比率和丙二醛(MDA)血浆水平已被提议作为监测自由基(FR)触发的氧化的重要标志物。在这里,我们描述了一种方便的现场扩增的样品注入毛细管电泳方法,该方法具有紫外线检测功能,用于分离和定量人血浆中的All,UA和游离MDA。血浆样品可通过离心膜管简单过滤以消除蛋白质,然后直接注入毛细管中,而无需进行复杂的纯化和/或样品衍生化程序。在电泳运行过程中,使用pH 300为300 mmol / L的硼酸钠与50 mmol / L的N-甲基-d-葡萄糖胺组成的运行缓冲液,在电泳运行过程中施加0.1 psi的过大压力/电压,可以实现碱性分离。在17分钟内分析物。电动进样可以使血浆样品中的全部检出限分别为15?nmol / L,UA的20?nmol / L和MDA的10?nmol / L,从而显着改善了上述基于毛细管电泳方法的LOD。精密度测试表明,我们的方法在迁移时间(CVα=?1.85%)和面积(CVα=?2.87%)方面都具有良好的重复性。而且,在测定内和测定间试验中都获得了良好的再现性(CVα=≥4.63%和CVα=≥6.59%)。通过测量40名健康志愿者的分析物水平来测试该方法的适用性。

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