Methods and limitations of stable isotope measurements via direct elution of chromatographic peaks using gas chromotography-Orbitrap mass spectrometry

Abstract

The Thermo Scientific™ QExactive Orbitrap™ mass spectrometer combined with a Thermo Scientific™ Trace™ 1310 GC enables high-mass-resolution measurements of molecular isotopic structure (e.g., molecular-average, position-specific, and multiple substitution measurements), but thus far has employed non-traditional, slow sample introduction methods and long integrations lasting minutes or tens of minutes to optimize measurement precision. This study examines the performance of the Orbitrap for isotope ratio measurements of analytes eluting directly from the gas chromatograph (GC) as traditional GC peaks — i.e. eluting over a period of seconds and with rapidly varying signal intensities. Such a measurement holds potential for simultaneous compound identification and isotope ratio measurement of numerous analytes separated by GC within a single acquisition. We applied this "direct elution" measurement strategy to molecular and fragment ions of para-xylene, serine, and a mixture of polycyclic aromatic hydrocarbons (PAHs) at natural isotope abundances. We built a mathematical model and used a Monte Carlo simulation to evaluate how variations in data processing decisions and GC peak characteristics (e.g., peak shape and elution timing) affect the accuracy of the resulting absolute isotope ratios and sample-standard comparisons (δ values). These case studies inform our recommendations for applying direct elution measurements. The method is appropriate for systems with large position-specific, molecular, or multiply-substituted isotopic anomalies (e.g., isotopically labelled or extraterrestrial compounds), and for compounds that produce strong molecular ions. Precisions improve when experiments are designed to (1) target ions with relatively high mass spectral intensities, (2) optimize the number of ions and range of masses admitted into the Orbitrap, and (3) minimize the nominal resolution settings while still separating relevant isobars.

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