| Literature DB >> 8831959 |
D H Fisher1, M I Broudy, L M Fisher.
Abstract
A method was developed for quantitating 9-carboxy-11-nor-delta 9-tetrahydrocannabinol in human urine as part of the process for validating an automated enzyme immunoassay for marijuana metabolites. Sample cleanup was accomplished using a mixed-mode solid-phase extraction. 9-Carboxy-11-nor-delta 9-tetrahydrocannabinol and the internal standard, brominated 9-carboxy-11-nor-delta 9-tetrahydrocannabinol, were quantified using high-performance liquid chromatography with electrochemical detection (+ 0.85 V). The linear range for this method is 0.012-0.20 microgram/mL. No interference was seen for 22 drugs and metabolites. The pooled relative standard deviation is 4.1% (n = 27) for the quality control samples. This method was compared to gas chromatography with mass spectrometry by linear regression analysis. The slope of the line is 1.00 +/- 0.05 (standard error), the intercept is approximately zero, the coefficient of determination is 0.994, and the standard error of the estimate is 0.006 microgram/mL.Entities:
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Year: 1996 PMID: 8831959 DOI: 10.1002/(SICI)1099-0801(199607)10:4<161::AID-BMC579>3.0.CO;2-3
Source DB: PubMed Journal: Biomed Chromatogr ISSN: 0269-3879 Impact factor: 1.902