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Drug Monitoring and Toxicology |
Departments of
1
Chemistry and
2
Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, V6T 2B5 Canada.
a Address correspondence to this author at: Department of Pathology and Laboratory Medicine, University of British Columbia, 2211 Wesbrook Mall, Vancouver, B.C., V6T 2B5 Canada. Fax 604-822-7635;
A new antibody to lysergic acid diethylamide (LSD) was used to develop a novel indirect ELISA for the quantification of drug in urine. Evaluation of the new assay with the commercially available LSD ELISA (STC Diagnostics) shows improved performance. The test requires 50 µL of urine, which is used to measure concentrations of drug in the µg/L to ng/L range. The limit of detection was 8 ng/L compared with 85 ng/L in the commercial assay, and analytical recoveries were 98106%. Our test detected 0.1 µg/L of LSD in urine with an intraassay CV of 2.4% (n = 8) compared with 6.0% for a 0.5 µg/L sample in the commercial assay (n = 20). The upper and lower limits of quantification were estimated to be 7 µg/L and 50 ng/L, respectively. Specificity was evaluated by measuring the extent of cross-reactivity with 24 related substances. Drug determination using the new assay offers both improved sensitivity and precision compared with existing methods, thus facilitating the preliminary quantitative estimation of LSD in urine at lower concentrations with a greater degree of certainty.
The following articles in journals at HighWire Press have cited this article:
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G. Skopp, L. Potsch, R. Mattern, and R. Aderjan Short-Term Stability of Lysergic Acid Diethylamide (LSD), N-Desmethyl-LSD, and 2-Oxo-3-hydroxy-LSD in Urine, Assessed by Liquid Chromatography-Tandem Mass Spectrometry Clin. Chem., September 1, 2002; 48(9): 1615 - 1618. [Full Text] [PDF] |
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