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DOI 10.1016/j.cca.2020.08.014

Медицинская библиотека · Clinica chimica acta; international journal of clinical chemistry · 2020

Urinary cannabinoid mass spectrometry profiles differentiate dronabinol from cannabis use.

Koch Christopher D, Xu Liang, Curtis Susanna A, Roberts John D, Bunch Dustin R, El-Khoury Joe M

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Аннотация

BACKGROUND

Dronabinol is used to treat a variety of conditions, including loss of appetite in people with AIDS and severe nausea and vomiting caused by cancer chemotherapy. Its therapeutic potential for pain management is now being explored in specific populations. Monitoring dronabinol compliance is challenging because its active ingredient, Δ-9-tetrahydrocannabinol (THC), is also present in cannabis. We developed a rapid LC-MS/MS assay with minimal specimen preparation to quantitate 11 cannabinoids in urine. Using this assay coupled with urine samples from normal controls, cannabis, and dronabinol users, we show the ability to differentiate cannabis from dronabinol use.

METHODS

Residual clinical urine samples from 55 cannabinoid positive subjects and 31 negative controls, as well as prospective samples from 5 patients receiving dronabinol therapy were obtained for analysis.

RESULTS

In the dronabinol group, only the THC metabolites 11-nor-9-carboxy-tetrahydrocannabinol (THC-COOH) and 11-hydroxy-Δ-9-tetrahydrocannabinol (THC-OH) were detected. Minor cannabinoids were detected in 91% of cannabis group samples and their detection was more frequent in samples with increased THC metabolite concentrations. Of minor cannabinoids evaluated, cannabigerol (CBG) and cannabidiol (CBD) had the greatest sensitivity in detecting cannabis use.

CONCLUSIONS

This method has a high sensitivity for the detection of cannabis use with implications for evaluating dronabinol compliance.

Для цитирования: Koch Christopher D, Xu Liang, Curtis Susanna A, Roberts John D, Bunch Dustin R, El-Khoury Joe M. Urinary cannabinoid mass spectrometry profiles differentiate dronabinol from cannabis use.. Clinica chimica acta; international journal of clinical chemistry. 2020. DOI: 10.1016/j.cca.2020.08.014.

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