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首页> 外文期刊>Analytical chemistry >Quantification of Cholesterol and Cholesteryl Ester by Direct Flow Injection High-Resolution Fourier Transform Mass Spectrometry Utilizing Species-Specific Response Factors
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Quantification of Cholesterol and Cholesteryl Ester by Direct Flow Injection High-Resolution Fourier Transform Mass Spectrometry Utilizing Species-Specific Response Factors

机译:通过直流喷射高分辨率傅立叶变换质谱法使用物种特异性响应因子的定量胆固醇和胆固醇酯

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摘要

The quantification of free cholesterol (FC) and cholesteryl ester (CE) in mammalian samples is of great interest for basic science and clinical lipidomics. Here, we evaluated the feasibility of direct flow injection analysis (FIA) coupled to electrospray ionization high-resolution mass spectrometry (ESI-HRMS) to quantify FC and CE in lipid extracts from human serum, cultured cells, and mouse liver. Despite poor ionization efficiency of FC, the limit of quantitation was sufficient for precise and accurate quantification of FC by multiplexed HRMS (MSX) analysis without using a derivatization step. However, it was demonstrated that, upon full scan Fourier transform MS (FTMS) quantification, CE species show substantial differences in their analytical responses depending on number of double bonds, length of the acyl chain, infused lipid concentration, and other lipid components. A major determinant for these response differences is their susceptibility to in-source fragmentation. In particular, introduction of double bonds lowers the degree of in-source fragmentation. Therefore, CE species-specific response factors need to be applied for CE quantification by FTMS to achieve accurate concentrations. Method validation demonstrated that FIA-ESI-HRMS (MSX and FTMS) is applicable for quantification of FC and CE in samples used in basic science as well as clinical studies such as cultured cells, tissue homogenates, and serum.
机译:哺乳动物样品中游离胆固醇(Fc)和胆固醇酯(CE)的定量对基础科学和临床脂质学具有很大的兴趣。这里,我们评估了直接流动注射分析(FIA)与电喷雾电离高分辨率质谱(ESI-HRMS)的可行性,以量化人血清,培养细胞和小鼠肝脏的脂质提取物中的Fc和Ce。尽管Fc的电离效率不佳,但通过多路复用的HRMS(MSX)分析,定量限制足以通过多路复用的HRMS(MSX)分析而不使用衍生步骤。然而,证明,在全扫描傅立叶变换MS(FTMS)定量时,CE物种根据双键的数量,酰基链的长度,注入脂浓度和其他脂质组分,CE物种在其分析响应中显示出显着差异。这些反应差异的主要决定因素是它们对源自裂缝的易感性。特别是,双键的引入降低了源自裂缝的程度。因此,CE物种特异性响应因子需要通过FTMS施加CE量化以实现准确的浓度。方法验证证明,FIA-ESI-HRMS(MSX和FTMS)适用于基础科学中使用的样品中的Fc和Ce的定量,以及培养细胞,组织匀浆和血清等临床研究。

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  • 来源
    《Analytical chemistry》 |2019年第5期|共8页
  • 作者单位

    Regensburg Univ Hosp Inst Clin Chem &

    Lab Med D-93042 Regensburg Germany;

    Univ Southern Denmark Dept Biochem &

    Mol Biol Villum Ctr Bioanalyt Sci Campusvej 55 DK-5230 Odense Denmark;

    Univ Southern Denmark Dept Biochem &

    Mol Biol Villum Ctr Bioanalyt Sci Campusvej 55 DK-5230 Odense Denmark;

    Regensburg Univ Hosp Inst Clin Chem &

    Lab Med D-93042 Regensburg Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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