Analysis of (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol and (–)-11-nor-9-carboxy-Δ8-tetrahydrocannabinol in hair from a school-age population
A sensitive liquid chromatography–tandem mass spectrometry method for the detection of (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol and (–)-11-nor-9-carboxy-Δ8-tetrahydrocannabinol in hair with a cutoff of 1 pg/10 mg of hair and a limit of quantitation of 0.2 pg/10 mg of hair for both analytes was d...
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Published in | Journal of analytical toxicology Vol. 49; no. 4; pp. 224 - 230 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
12.04.2025
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Subjects | |
Online Access | Get full text |
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Summary: | A sensitive liquid chromatography–tandem mass spectrometry method for the detection of (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol and (–)-11-nor-9-carboxy-Δ8-tetrahydrocannabinol in hair with a cutoff of 1 pg/10 mg of hair and a limit of quantitation of 0.2 pg/10 mg of hair for both analytes was developed and is herein described. A subset of samples collected from a school-age population between December 2022 and February 2023 was analyzed using this method after having screened presumptive positive by enzyme immunoassay out of a total pool of approximately 5300 samples. Of these presumptive positive samples, 66% showed the presence of one or both analytes at a concentration ≥1 pg/10 mg of hair. Of the 213 positive samples, 57% contained more (–)-11-nor-9-carboxy-Δ8-tetrahydrocannabinol than (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol and 6% contained more than 50-fold higher Δ8 isomer than Δ9 isomer. Of the 197 samples that were reportable for (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol ≥1 pg/10 mg cutoff, 53% of them contained more (–)-11-nor-9-carboxy-Δ8-tetrahydrocannabinol than (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol. Of the 197 samples that were reportable for (–)-11-nor-9-carboxy-Δ8-tetrahydrocannabinol ≥1 pg/10 mg cutoff, 15.7% exceeded the upper limit of linearity of the method (200 pg/10 mg). These results suggest a high level of (–)-Δ8-tetrahydrocannabinol usage in this population relative to (–)-Δ9-tetrahydrocannabinol usage. They further suggest the possibility that (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol reported for some of these samples may only have been present due to (–)-Δ9-tetrahydrocannabinol contamination of (–)-Δ8-tetrahydrocannabinol products being consumed in large quantities. Thus, reported results for (–)-11-nor-9-carboxy-Δ9-tetrahydrocannabinol alone may give a false picture of the extent of the cannabis product being consumed by a test subject. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0146-4760 1945-2403 1945-2403 |
DOI: | 10.1093/jat/bkaf020 |