首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >A simple and robust LC-MS/MS method for quantification of free 3-nitrotyrosine in human plasma from patients receiving on-pump CABG surgery
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A simple and robust LC-MS/MS method for quantification of free 3-nitrotyrosine in human plasma from patients receiving on-pump CABG surgery

机译:一种简单而强大的LC-MS / MS方法,用于定量接受CABG手术患者的血浆中的游离3-硝基酪氨酸

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摘要

We have developed a simple, sensitive, and robust liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) method to determine free 3-nitrotyrosine concentrations in human plasma of patients receiving on-pump coronary artery bypass grafting surgery. A one-step solid-phase extraction protocol was optimized to enrich the analyte at low nanomolar concentrations. The processed samples were analyzed by LC-MS/MS with a 2.1 × 100 mm Kinetex PFP column and a triple quadrupole mass spectrometer. The method was validated for 3-nitrotyrosine concentrations close to real patient plasma levels. The relative standard deviations or relative errors of the intraday and interday determinations were all within 10%. Limit of detection and limit of quantitation were determined to be 0.034 nM and 0.112 nM, respectively, while lower limit of quantitation was below 0.625 nM. No deterioration of the column performance was noticed after running a large number of patient samples. The results showed that the 3-nitrotyrosine concentrations in coronary sinus plasma samples were elevated after cardiopulmonary bypass (CPB) procedure. The pre-CPB and post-CPB concentrations of 3-nitrotyrosine in patient plasmas were 1.494 ± 0.107 nM and 2.167 ± 0.177 nM (mean ± SEM), respectively. Application of this method to more patients in clinical studies may help validate 3-nitrotyrosine as a meaningful biomarker for nitrosative stress and link patient characteristics, clinical outcomes, and cardioprotective treatments to endogenous nitrosative stress levels.
机译:我们已经开发了一种简单,灵敏且可靠的液相色谱-质谱/质谱(LC-MS / MS)方法,用于确定接受泵上冠状动脉搭桥术的患者血浆中游离的3-硝基酪氨酸浓度。优化了一步固相萃取方案,以在低纳摩尔浓度下富集分析物。通过LC-MS / MS用2.1×100 mm Kinetex PFP色谱柱和三重四极杆质谱仪分析处理后的样品。该方法已针对接近实际患者血浆水平的3-硝基酪氨酸浓度进行了验证。日内和日间测定的相对标准偏差或相对误差均在10%以内。检出限和定量限分别确定为0.034 nM和0.112 nM,而定量下限则低于0.625 nM。运行大量患者样品后,未发现色谱柱性能下降。结果表明,体外循环(CPB)后,冠状窦血浆样品中的3-硝基酪氨酸浓度升高。患者血浆中3-硝基酪氨酸的CPB前和CPB后浓度分别为1.494±0.107 nM和2.167±0.177 nM(平均值±SEM)。在临床研究中将这种方法应用于更多患者可能有助于验证3-硝基酪氨酸作为亚硝化应激的有意义的生物标志物,并将患者的特征,临床结果以及心脏保护性治疗与内源性亚硝化应激水平联系起来。

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