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发展微流超高效液相色谱-质谱代谢组学分析方法,用于分析哺乳动物生物体液。

Development of microflow ultra high performance liquid chromatography-mass spectrometry metabolomic assays for analysis of mammalian biofluids.

机构信息

School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

Defence Science and Technology Laboratory, Porton Down, Salisbury, SP4 0JQ, UK.

出版信息

Metabolomics. 2024 Oct 25;20(6):120. doi: 10.1007/s11306-024-02187-y.

Abstract

INTRODUCTION AND OBJECTIVES

The application of untargeted metabolomics assays using ultra high performance liquid chromatography-mass spectrometry (UHPLC-MS) to study metabolism in biological systems including humans is rapidly increasing. In some of these studies there is a requirement to collect and analyse low sample volumes of biofluids (e.g. tear fluid) or low cell and tissue mass samples (e.g. tissue needle biopsies). The application of microflow, capillary or nano liquid chromatography (≤ 1.0 mm column internal diameter (i.d.)) theoretically should accomplish a higher assay sensitivity compared to analytical liquid chromatography (2.1-5.0 mm column internal diameter). To date, there has been limited research into microflow UHPLC-MS assays that can be applied to study samples of low volume or mass.

METHODS

This paper presents three complementary UHPLC-MS assays (aqueous C reversed-phase, lipidomics C reversed-phase and Hydrophilic Interaction Liquid Chromatography (HILIC)) applying 1.0 mm internal diameter columns for untargeted metabolomics. Human plasma and urine samples were applied for the method development, with porcine plasma, urine and tear fluid used for method assessment. Data were collected and compared for columns of the same length, stationary phase and stationary phase particle size but with two different column internal diameters (2.1 mm and 1.0 mm).

RESULTS AND CONCLUSIONS

All three assays showed an increase in peak areas and peak widths when applying the 1.0 mm i.d. assays. HILIC assays provide an advantage at lower sample dilutions whereas for reversed phase (RP) assays there was no benefit added. This can be seen in the validation study where a much higher number of compounds were detected in the HILIC assay. RP assays were still appropriate for small volume samples with hundreds of compounds being detected. In summary, the 1.0 mm i.d. column assays are applicable for small volume samples where dilution is required during sample preparation.

摘要

简介和目的

使用超高效液相色谱-质谱联用(UHPLC-MS)进行非靶向代谢组学分析在研究包括人类在内的生物系统代谢方面的应用正在迅速增加。在这些研究中,有些需要收集和分析低体积的生物流体(如泪液)或低细胞和组织质量的样品(如组织针活检)。微流、毛细管或纳米液相色谱(≤1.0 毫米内径(ID))的应用理论上应该比分析液相色谱(2.1-5.0 毫米内径)具有更高的分析灵敏度。迄今为止,对于可应用于研究低体积或低质量样品的微流 UHPLC-MS 分析方法的研究有限。

方法

本文提出了三种互补的 UHPLC-MS 分析方法(水性 C 反相、脂质组学 C 反相和亲水相互作用液相色谱(HILIC)),应用 1.0 毫米内径的色谱柱进行非靶向代谢组学分析。人血浆和尿液样品用于方法开发,猪血浆、尿液和泪液用于方法评估。收集和比较了相同长度、固定相和固定相粒径但具有两种不同内径(2.1 毫米和 1.0 毫米)的色谱柱的数据。

结果和结论

当应用 1.0 毫米内径的分析方法时,所有三种分析方法的峰面积和峰宽都有所增加。HILIC 分析方法在较低的样品稀释度下具有优势,而对于反相(RP)分析方法,则没有额外的好处。这在验证研究中可以看出,HILIC 分析方法检测到的化合物数量要多得多。RP 分析方法仍然适用于需要在样品制备过程中进行稀释的小体积样品。总的来说,1.0 毫米内径的色谱柱分析方法适用于需要在样品制备过程中进行稀释的小体积样品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0d9/11511728/c58815f94000/11306_2024_2187_Fig1_HTML.jpg

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