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Published:
Journal of Analytical Toxicology,
ISSN 0146-4760,
Volume 32, Number 3, April,
pp.220-226
Development
and Validation of ELISA and GC–MS Procedures for the Quantification
of Dextromethorphan and its Main Metabolite Dextrorphan in Urine
and Oral Fluid
Warren C. Rodrigues, Guohong Wang, Christine Moore, Alpana Agrawal,
Michael J. Vincent, and James R. Soares
Immunalysis Corporation, 829 Towne Center Drive, Pomona, California
91767
The development of a highly sensitive enzyme-linked
immunosorbent assay and gas chromatography–mass spectrometry
confirmation method for the detection of dextromethorphan and
its major metabolite dextrorphan in urine and oral fluid is described.
For the screening assay, the intraday precision was less than
8% for urine and less than 5% for oral fluid. The interday precision
was less than 10% for both drugs in urine and oral fluid. For
the confirmatory procedure, both inter- and intraday precision
was less than 5% for both matrices. The detection limit for both
methods was 1 ng/mL. The quantifying ions chosen from the full
scan mass spectra were m/z 271 for dextromethorphan, m/z
329 for dextrorphan, and m/z 332 for tri-deuterated
dextrorphan-d3.
A high recovery yield (> 93%) from the Quantisal™ oral
fluid collection device was achieved, and the drugs were stable
in the collection device for at least 10 days at room temperature.
The extracted drugs from both matrices were stable for at least
48 h while kept at room temperature. Both screening and confirmatory
procedures were applied to authentic urine and oral fluid specimens
obtained from volunteers following therapeutic ingestion of dextromethorphan.
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