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Direct infusion electrospray ionization-ion mobility-mass spectrometry for comparative profiling of fatty acids based on stable isotope labeling

机译:直接注入电喷雾电离离子淌度质谱用于基于稳定同位素标记的脂肪酸比较分析

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A rapid method for fatty acids (FAs) comparative profiling based on carboxyl-specific stable isotope labeling (SIL) and direct infusion electrospray ionization-ion mobility-mass spectrometry (ESI-IM-MS) is established. The design of the method takes advantage of the three-dimensional characteristics of IM -MS including drift time, m/z and ion intensity, for comparison of d0-/d6-2,4-dimethoxy-6-piperazin-1-yl pyrimidine (DMPP)-labeled FAs. In particular, without chromatographic separation, the method allowed direct FAs profiling in complex samples due to the advantageous priority of DMPP in signal enhancement as well as the extra resolution that IM-MS offered. Additionally, the d0-/d6-DMPP-labeled FAs showed expected features, including very similar drift times, 6 Da mass deviations, specific reporter ions, similar MS responses, and adherence to the drift time rule regarding the influence of carbon chain length and unsaturation on relative drift times. Therefore, the introduction of isotope analogs minimized the matrix effect and variations in quantification and ensured accurate identification of non-targeted FAs by those typical features. Peak intensity ratios between d0-/d6-DMPP-labeled ions were subsequently used in relative quantification for the detected FAs. The established strategy has been applied successfully in the rapid profiling of trace free FAs between normal and cancerous human thyroid tissues. Sixteen free FAs were found with the increased level with a statistically significant difference (p < 0.05) compared to the normal tissue samples. The integrated SIL technique and ESI-IM-MS are expected to serve as an alternative tool for high-throughput analysis of FAs in complex samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:建立了一种基于羧基特异性稳定同位素标记(SIL)和直接注入电喷雾电离离子淌度质谱(ESI-IM-MS)的脂肪酸(FAs)比较分析的快速方法。该方法的设计利用了IM -MS的三维特征,包括漂移时间,m / z和离子强度,用于比较d0- / d6-2,4-二甲氧基-6-哌嗪-1-基嘧啶(DMPP)标记的FA。尤其是,在没有色谱分离的情况下,由于DMPP在信号增强方面的优先权以及IM-MS提供的额外分辨率,该方法允许在复杂样品中直接进行FA分析。此外,d0- / d6-DMPP标记的FA表现出预期的特征,包括非常相似的漂移时间,6 Da质量偏差,特定的报告离子,相似的MS响应以及遵守关于碳链长度和相对漂移时间不饱和。因此,同位素类似物的引入最大程度地降低了基质效应和定量变化,并确保通过这些典型特征准确识别非目标FA。 d0- / d6-DMPP标记离子之间的峰强度比随后用于检测到的FA的相对定量。既定的策略已成功应用于正常和癌性人类甲状腺组织之间的痕量游离FA的快速分析。与正常组织样品相比,发现了十六种游离FA,其水平升高,具有统计学上的显着差异(p <0.05)。集成的SIL技术和ESI-IM-MS有望作为高通量分析复杂样品中FA的替代工具。 (C)2015 Elsevier B.V.保留所有权利。

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