» Articles » PMID: 27143232

Analysis of Polar Urinary Metabolites for Metabolic Phenotyping Using Supercritical Fluid Chromatography and Mass Spectrometry

Overview
Journal J Chromatogr A
Publisher Elsevier
Specialty Chemistry
Date 2016 May 5
PMID 27143232
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

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 alkylamine 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 7min gradient SFC method, where the use of the recommended column and co-solvent combination resulted in a significant improvement in chromatographic performance.

Citing Articles

(Pre)Clinical Metabolomics Analysis.

Pebriana R, Sanchez-Lopez E, Giera M Methods Mol Biol. 2024; 2855:3-19.

PMID: 39354298 DOI: 10.1007/978-1-0716-4116-3_1.


Applications of chromatographic methods in metabolomics: A review.

Ovbude S, Sharmeen S, Kyei I, Olupathage H, Jones J, Bell R J Chromatogr B Analyt Technol Biomed Life Sci. 2024; 1239:124124.

PMID: 38640794 PMC: 11618781. DOI: 10.1016/j.jchromb.2024.124124.


Simultaneous Quantitative Analysis of the Major Bioactive Compounds in and its Beverages by UHPSFC-DAD.

Gibitz-Eisath N, Seger C, Schwaiger S, Sturm S, Stuppner H J Agric Food Chem. 2022; 70(24):7586-7593.

PMID: 35695390 PMC: 9228070. DOI: 10.1021/acs.jafc.2c01584.


High Throughput Semiquantitative UHPSFC-MS/MS Lipid Profiling and Lipid Class Determination.

Bartosova Z, Gonzalez S, Voigt A, Bruheim P J Chromatogr Sci. 2021; 59(7):670-680.

PMID: 33479755 PMC: 8217741. DOI: 10.1093/chromsci/bmaa121.


Comprehensive and Reproducible Untargeted Lipidomic Workflow Using LC-QTOF Validated for Human Plasma Analysis.

Forest A, Ruiz M, Bouchard B, Boucher G, Gingras O, Daneault C J Proteome Res. 2018; 17(11):3657-3670.

PMID: 30256116 PMC: 6572761. DOI: 10.1021/acs.jproteome.8b00270.

References
1.
Lee J, Nagai T, Gotoh N, Fukusaki E, Bamba T . Profiling of regioisomeric triacylglycerols in edible oils by supercritical fluid chromatography/tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2014; 966:193-9. DOI: 10.1016/j.jchromb.2014.01.040. View

2.
Want E, Wilson I, Gika H, Theodoridis G, Plumb R, Shockcor J . Global metabolic profiling procedures for urine using UPLC-MS. Nat Protoc. 2010; 5(6):1005-18. DOI: 10.1038/nprot.2010.50. View

3.
Regalado E, Helmy R, Green M, Welch C . Chromatographic resolution of closely related species: drug metabolites and analogs. J Sep Sci. 2014; 37(9-10):1094-102. DOI: 10.1002/jssc.201400038. View

4.
De Klerck K, Mangelings D, Clicq D, De Boever F, Vander Heyden Y . Combined use of isopropylamine and trifluoroacetic acid in methanol-containing mobile phases for chiral supercritical fluid chromatography. J Chromatogr A. 2011; 1234:72-9. DOI: 10.1016/j.chroma.2011.11.023. View

5.
Smith R . Supercritical fluids in separation science--the dreams, the reality and the future. J Chromatogr A. 1999; 856(1-2):83-115. DOI: 10.1016/s0021-9673(99)00617-2. View