Evaluation of isotopically labeled internal standards and methods of derivatization for quantitative determination of cocaine and related compounds
Abstract Gas chromatography-mass spectrometry (GCMS) is the preferred method for the analysis of drugs/metabolites in biological specimens
with use of isotopically labeled analogs of the analytes as internal standards (ISs). An important aspect of the chemical
derivatization (CD) for GC-MS analysis is that the CD products derived from the analyte and the selected IS must generate
ions suitable for designating the analyte and the IS. These ions should not have significant cross contribution (CC), i.e.,
IS contribution to the intensities of the ions designated for the analyte, and vice versa. With this in mind, the authors
have conducted a search of isotopically labeled analogs of commonly abused cocaine and related compounds (cocaine, norcocaine,
benzoylecgonine, cocaethylene, ecgonine, ecgonine methyl ester, anhydroecgonine methyl ester) that are commercially available.
These ISs and analytes were derivatized with various groups of reagents, and the CD products were analyzed by GC-MS. MS data
are presented in two forms: (1) systematic presentation of fullscan spectra; and (2) tabulation of CC data for ions with potential
for designating the ISs and analytes. Many (if not most) of these full-scan spectra are not yet available in the open literature
and should be of routine reference value to forensic and clinical laboratories that are engaged in the analysis of these drugs/metabolites.
Fullscan MS data were further used to select ion pairs with potential for designating the analytes and ISs in quantitative
analysis protocols. The CC data of these ion pairs were evaluated using data collected under the selected ion-monitoring mode
and summarized in table format. The data exhibited similar CC characteristics in each alkyl, acetyl, or TMS series. Among
the potentially usable ion pairs derived from a specific CD group, there was a trend that the ion pairs with higher mass showed
better CC data. The CC data derived from the use of ISs labeled with more deuterium atoms were generally more favorable. These
data should save enormous amounts of time and effort for practicing laboratories in their search for optimal analytical parameters.
Content TypeJournal Article
JournalForensic ToxicologyOnline ISSN 1860-8973Print ISSN 1860-8965
Journal VolumeVolume 24
Journal IssueVolume 24, Number 1 / July, 2006 (Source: Forensic Toxicology)
- Determination of some antiallergic drugs in human plasma by direct-injection high-performance liquid chromatography-tandem mass spectrometry
- Gc-ms detection and tentative characterization of two noscapine metabolites in human urine and their potential as markers for opium and illicit heroin use
- Stability of cocaine in formalin solution and fixed tissues
- Simultaneous analysis of six phenethylamine-type designer drugs by tlc, lc-ms, and gc-ms
- High throughput analysis of drugs of abuse in hair by combining purposely designed sample extraction compatible with immunometric methods used for drug testing in urine
