Analysis of polar urinary metabolites for metabolic phenotyping using supercritical fluid chromatography and mass spectrometry

被引:48
作者
Sen, Arundhuti [1 ,3 ]
Knappy, Christopher [1 ,2 ,3 ]
Lewis, Matthew R. [3 ]
Plumb, Robert S. [2 ,4 ]
Wilson, Ian D. [2 ]
Nicholson, Jeremy K. [2 ,3 ]
Smith, Norman W. [1 ]
机构
[1] Kings Coll London, Fac Life Sci & Med, Analyt & Environm Sci Div, Franklin Wilkins Bldg, London SE1 9NH, England
[2] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Surg & Canc, Computat & Syst Med, Sir Alexander Fleming Bldg,South Kensington Campu, London SW7 2DD, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Surg & Canc, Hammersmith Hosp, MRC NIHR Natl Phenome Ctr,Div Computat & Syst Med, IRDB Bldg, London W12 0NN, England
[4] Waters Corp, Milford, MA USA
基金
英国医学研究理事会;
关键词
SFC; Method development; Polar; Stationary phase; Modifier; Additive; STATIONARY PHASES; MOBILE-PHASE; SEPARATION; DRUGS; ANALYTES; WATER;
D O I
10.1016/j.chroma.2016.04.040
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Supercritical fluid chromatography (SFC) is frequently used for the analysis and separation of non-polar metabolites, but remains relatively underutilised for the study of polar molecules, even those which pose difficulties with established reversed-phase (RP) or hydrophilic interaction liquid chromatographic (HILIC) methodologies. Here, we present a fast SFC-MS method for the analysis of medium and high polarity (-7 <= cLogP <= 2) compounds, designed for implementation in a high-throughput metabonomics setting. Sixty polar analytes were first screened to identify those most suitable for inclusion in chromatographic test mixtures; then, a multi-dimensional method development study was conducted to determine the optimal choice of stationary phase, modifier additive and temperature for the separation of such analytes using SFC. The test mixtures were separated on a total of twelve different column chemistries at three different temperatures, using CO2-methanol-based mobile phases containing a variety of polar additives. Chromatographic performance was evaluated with a particular emphasis on peak capacity, overall resolution, peak distribution and repeatability. The results suggest that a new generation of stationary phases, specifically designed for improved robustness in mixed CO2-methanol mobile phases, can improve peak shape, peak capacity and resolution for all classes of polar analytes. A significant enhancement in chromatographic performance was observed for these urinary metabolites on the majority of the stationary phases when polar additives such as ammonium salts (formate, acetate and hydroxide) were included in the organic modifier, and the use of water or allcylamine additives was found to be beneficial for specific subsets of polar analytes. The utility of these findings was confirmed by the separation of a mixture of polar metabolites in human urine using an optimised 7 min gradient SFC method, where the use of the recommended column and co-solvent combination resulted in a significant improvement in chromatographic performance. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 155
页数:15
相关论文
共 43 条
  • [21] Spectroscopic and Statistical Techniques for Information Recovery in Metabonomics and Metabolomics
    Lindon, John C.
    Nicholson, Jeremy K.
    [J]. ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, 2008, 1 (45-69) : 45 - 69
  • [22] Theory of peak capacity in gradient elution
    Neue, UD
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2005, 1079 (1-2) : 153 - 161
  • [23] Metabolic phenotyping in clinical and surgical environments
    Nicholson, Jeremy K.
    Holmes, Elaine
    Kinross, James M.
    Darzi, Ara W.
    Takats, Zoltan
    Lindon, John C.
    [J]. NATURE, 2012, 491 (7424) : 384 - 392
  • [24] Ultra high performance supercritical fluid chromatography coupled with tandem mass spectrometry for screening of doping agents. I: Investigation of mobile phase and MS conditions
    Novakova, Lucie
    Perrenoud, Alexandre Grand-Guillaume
    Nicoli, Raul
    Saugy, Martial
    Veuthey, Jean-Luc
    Guillarme, Davy
    [J]. ANALYTICA CHIMICA ACTA, 2015, 853 : 637 - 646
  • [25] Elution and preliminary structure-retention modeling of polar and ionic substances in fluid chromatography using volatile ammonium salts as mobile hase additives
    Pinkston, JD
    Stanton, DT
    Wen, D
    [J]. JOURNAL OF SEPARATION SCIENCE, 2004, 27 (1-2): : 115 - 123
  • [26] Stationary phases for packed-column supercritical fluid chromatography
    Poole, Colin F.
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2012, 1250 : 157 - 171
  • [27] Pournelle G. H., 1953, Journal of Mammalogy, V34, P133, DOI 10.1890/0012-9658(2002)083[1421:SDEOLC]2.0.CO
  • [28] 2
  • [29] Chromatographic resolution of closely related species: Drug metabolites and analogs
    Regalado, Erik L.
    Helmy, Roy
    Green, Mitchell D.
    Welch, Christopher J.
    [J]. JOURNAL OF SEPARATION SCIENCE, 2014, 37 (9-10) : 1094 - 1102
  • [30] History of supercritical fluid chromatography: Instrumental development
    Saito, Muneo
    [J]. JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2013, 115 (06) : 590 - 599