Sequential Hybrid Three-Dimensional Gas Chromatography with Accurate Mass Spectrometry: A Novel Tool for High-Resolution Characterization of Multicomponent Samples
Version 2 2024-06-05, 00:49Version 2 2024-06-05, 00:49
Version 1 2018-08-07, 08:30Version 1 2018-08-07, 08:30
journal contribution
posted on 2024-06-05, 00:49 authored by DD Yan, YF Wong, SP Whittock, A Koutoulis, Robert ShellieRobert Shellie, PJ Marriott© 2018 American Chemical Society. A novel sequential three-dimensional gas chromatography-high-resolution time-of-flight mass spectrometry (3D GC-accTOFMS) approach for profiling secondary metabolites in complex plant extracts is described. This integrated system incorporates a nonpolar first-dimension (1Dnp) separation step, prior to a microfluidic heart-cut (H/C) of a targeted region(s) to a cryogenic trapping device, directly followed by the rapid reinjection of a trapped solute into a polar second-dimension (2DPEG) column for multidimensional separation (GCnp-GCPEG). For additional separation, the effluent from2DPEGcan then be modulated according to a comprehensive 2D GC process (GC×GC), using an ionic liquid phase as a third-dimension (3DIL) column, to produce a sequential GCnp-GCPEG×GCILseparation. Thus, the unresolved or poorly resolved components, or regions that require further separation, can be precisely selected and rapidly transferred for additional separation on2D or3D columns, based on the greater separation realized by these steps. The described integrated system can be used in a number of modes, but one useful approach is to target specific classes of compounds for improved resolution. This is demonstrated through the separation and detection of the oxygenated sesquiterpenes in hop (Humulus lupulus L.) essential oil and agarwood (Aquilaria malaccensis) oleoresin. Improved resolution and peak capacity were illustrated through the progressive comparison of the tentatively identified components for GCnp-GCPEGand GCnp-GCPEG×GCILmethods. Relative standard deviations of intraday retentions (1tR,2tR,, and3tR) and peak areas of ≤0.01, 0.07, 0.71, and 7.5% were achieved. This analytical approach comprising three GC column selectivities, hyphenated with high-resolution TOFMS detection, should be a valuable adjunct for the improved characterization of complex plant samples, particularly in the area of plant metabolomics.
History
Journal
Analytical ChemistryVolume
90Pagination
5264-5271Location
United StatesISSN
0003-2700eISSN
1520-6882Language
EnglishPublication classification
C1 Refereed article in a scholarly journalCopyright notice
2018, American Chemical SocietyIssue
8Publisher
AMER CHEMICAL SOCUsage metrics
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Keywords
Science & TechnologyPhysical SciencesChemistry, AnalyticalChemistryLIQUID STATIONARY-PHASEPLANT METABOLOMICSIDENTIFICATIONVOLATILESGENOTYPESFLAVORCOLUMNOILS030108 Separation Science060705 Plant Physiology970103 Expanding Knowledge in the Chemical Sciences970106 Expanding Knowledge in the Biological SciencesLP140100160School of Exercise and Nutrition Sciences3401 Analytical chemistry
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