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Published:
Journal of Analytical Toxicology,
ISSN 0146-4760,
Volume 24,
Number 7, October,
pp. 595-601
Here is where the title stuff goes
Assessment
of the Ion-Trap Mass Spectrometer for Routine Qualitative and Quantitative Analysis
of Drugs of Abuse Extracted from Urine
Shawn
P. Vorce, Jason H. Sklerov, and Kathryn S. Kalasinsky
Office of the Armed Forces Medical Examiner, Division of Forensic Toxicology,
Armed Forces Institute of Pathology, 1413 Research Boulevard, Building 102,
Rockville, Maryland 20850-3125
The
ion-trap mass spectrometer (MS) has been available as a detector for gas chromatography
(GC) for nearly two decades. However, it still occupies a minor role in forensic
toxicology drug-testing laboratories. Quadrupole MS instruments make up the
majority of GC detectors used in drug confirmation. This work addresses the
use of these two MS detectors, comparing the ion ratio precision and quantitative
accuracy for the analysis of different classes of abused drugs extracted from
urine. Urine specimens were prepared at five concentrations each for amphetamine
(AMP), methamphetamine (METH), benzoylecgonine (BZE), D9-carboxy-tetrahydrocannabinol
(D9-THCCOOH), phencyclidine (PCP), morphine (MOR), codeine (COD), and 6-acetylmorphine
(6-AM). Concentration ranges for AMP, METH, BZE, D9-THCCOOH, PCP, MOR, COD,
and 6-AM were 502500, 505000, 15800, 1.565, 1250,
50032000, 25021000, and 1.5118 ng/mL, respectively. Sample
extracts were injected into a GCquadrupole MS operating in selected ion
monitoring (SIM) mode and a GCion-trap MS operating in either selected
ion storage (SIS) or full scan (FS) mode. Precision was assessed by the evaluation
of five ion ratios for n = 15 injections at each concentration using a single-point
calibration. Precision measurements for SIM ion ratios provided coefficients
of variation (CV) between 2.6 and 9.8% for all drugs. By comparison, the SIS
and FS data yielded CV ranges of 4.012.8% and 4.011.2%, respectively.
The total ion ratio failure rates were 0.2% (SIM), 0.7% (SIS), and 1.2% (FS)
for the eight drugs analyzed. Overall, the SIS mode produced stable, comparable
mean ratios over the concentration ranges examined, but had greater variance
within batch runs. Examination of postmortem and quality-control samples produced
forensically accurate quantitation by SIS when compared to SIM. Furthermore,
sensitivity of FS was equivalent to SIM for all compounds examined except for
6-AM.
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