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基于尿液样本和直接进样质谱法的代谢组学方法的开发。

Development of a metabolomic approach based on urine samples and direct infusion mass spectrometry.

作者信息

González-Domínguez Raúl, Castilla-Quintero Rocío, García-Barrera Tamara, Gómez-Ariza José Luis

机构信息

Department of Chemistry and CC.MM, Faculty of Experimental Science, Campus de El Carmen, University of Huelva, 21007 Huelva, Spain; International Campus of Excellence on Agrofood (CEIA3), University of Huelva, 21007 Huelva, Spain; Research Center of Health and Environment (CYSMA), Campus de El Carmen, University of Huelva, 21007 Huelva, Spain.

Department of Chemistry and CC.MM, Faculty of Experimental Science, Campus de El Carmen, University of Huelva, 21007 Huelva, Spain; International Campus of Excellence on Agrofood (CEIA3), University of Huelva, 21007 Huelva, Spain; Research Center of Health and Environment (CYSMA), Campus de El Carmen, University of Huelva, 21007 Huelva, Spain.

出版信息

Anal Biochem. 2014 Nov 15;465:20-7. doi: 10.1016/j.ab.2014.07.016. Epub 2014 Jul 23.

Abstract

The analysis of urine by direct infusion mass spectrometry suffers from ion suppression due to its high salt content and inter-sample variability caused by the differences in urine volume between persons. Thus, urine metabolomics requires a careful selection of the sample preparation procedure and a normalization strategy to deal with these problems. Several approaches were tested for metabolomic analysis of urine samples by direct infusion electrospray mass spectrometry (DI-ESI-MS), including solid phase extraction, liquid-liquid extraction, and sample dilution. In addition, normalization of results based on conductivity values and statistical treatment was performed to minimize sample variability. Both urine dilution and solid phase extraction with mixed mode sorbent considerably reduced the salt content in urine, providing comprehensive metabolomic fingerprints. Moreover, statistical data normalization enabled the correction of inter-sample physiological variability, improving the quality of results obtained. Therefore, high-throughput DI-ESI-MS fingerprinting of urine samples can be achieved with simple pretreatment procedures allowing the use of this noninvasive sampling in metabolomics. Finally, the optimized approach was tested in a pilot metabolomic investigation of urine samples from transgenic mice models of Alzheimer's disease (APP/PS1) in order to illustrate the potential of the methodology.

摘要

直接进样质谱法分析尿液时,由于其高盐含量会导致离子抑制,且不同人尿液体积的差异会引起样本间的变异性。因此,尿液代谢组学需要仔细选择样品制备程序和归一化策略来处理这些问题。通过直接进样电喷雾质谱法(DI-ESI-MS)对尿液样本进行代谢组学分析测试了几种方法,包括固相萃取、液液萃取和样品稀释。此外,基于电导率值进行结果归一化并进行统计处理,以尽量减少样品变异性。尿液稀释和使用混合模式吸附剂的固相萃取都大大降低了尿液中的盐含量,提供了全面的代谢组学指纹图谱。此外,统计数据归一化能够校正样本间的生理变异性,提高所得结果的质量。因此,通过简单的预处理程序可以实现尿液样本的高通量DI-ESI-MS指纹图谱分析,从而能够在代谢组学中使用这种非侵入性采样方法。最后,在阿尔茨海默病(APP/PS1)转基因小鼠模型尿液样本的初步代谢组学研究中测试了优化后的方法,以说明该方法的潜力。

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