Isotopic Analogs as Internal Standards for Quantitative GC/MS Analysis—Molecular Abundance and Retention Time Difference as Interference Factors

    Volume 47, Issue 4 (July 2002)

    ISSN: 0022-1198

    CODEN: JFSOAD

    Published Online: 1 July 2002

    Page Count: 9


    Smith, J
    Graduate student and professor and program director, University of,

    Liu, RH
    Graduate student and professor and program director, University of,

    Chang, WT
    Professor, Central,

    (Received 22 January 2002; accepted 14 January 2002)

    Abstract

    The following analyte/isotope-labeled internal standard (IS) systems are adapted to further study the interference phenomenon previously reported from our laboratory—the intensity ratio of the ion-pair designated for a specific analyte/2H-analog system increases as the solvent used to reconstitute the extraction/derivatization residue is increased: (a) Three analyte/2H-analog pairs with 2H-atoms positioned at allylic sites (butalbital, secobarbital, methohexital); (b) Two analyte/2H-analog pairs without these structural features (pentobarbital, phenobarbital); and (c) Two analyte/13C-analog pairs (butalbital, secobarbital). Major experimental parameters adapted in this study include: (a) Varying reconstitution solvent volume while keeping a constant analyte/IS concentration ratio; (b) Varying analyte/IS concentration ratio; (c) Varying gas chromatograph (GC) injection port temperature; and (d) Varying GC column temperature programming conditions, rendering difference in the degree of overlap of the peaks derived from the analyte and the 2H-analog. This study results in the following observations: (a) Changes in the intensity ratio of the ionpair designated for a specific analyte/2H-analog system depend on molecular abundance, regardless of whether the 2H-atoms are positioned at active allylic positions or not—thus, ruling out hydrogen/deuterium exchange as the cause of the observed interference phenomenon; (b) Variations in GC injection port temperature do not alter the observed interference phenomenon—thus, ruling out chemical reactions at the injection port as the underlying cause; (c) Variations in peak-overlapping between the analyte and the 2H-analog, facilitated by changing GC column programming conditions, alter the observed interference phenomenon. Abundance of the analyte and the 2H-analog and their overlapping characteristic in the mass spectrometer ion source are believed to be the underlying cause of the observed interference phenomenon. The interference phenomenon observed for a specific analyte/2H-analog system has significant consequences on the linearity of the thereby generated calibration curves. Nonlinear approaches can better describe the calibration data and are needed more in comparison to systems in which 13C-analogs are used as the ISs.


    Paper ID: JFS15451J

    DOI: 10.1520/JFS15451J

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    Title Isotopic Analogs as Internal Standards for Quantitative GC/MS Analysis—Molecular Abundance and Retention Time Difference as Interference Factors
    Symposium , 0000-00-00
    Committee E30