Detection of Δ9‐tetrahydrocannabinol (THC) in oral fluid using two point‐of‐collection testing devices following oral administration of a THC and cannabidiol containing oil

Author:

Suraev Anastasia1234ORCID,McCartney Danielle134ORCID,Kevin Richard156,Gordon Rebecca1,Grunstein Ronald R.278,Hoyos Camilla M.29,McGregor Iain S.134

Affiliation:

1. Lambert Initiative for Cannabinoid Therapeutics University of Sydney Sydney New South Wales Australia

2. Centre for Sleep and Chronobiology Woolcock Institute of Medical Research Sydney New South Wales Australia

3. School of Psychology, Faculty of Science University of Sydney Sydney New South Wales Australia

4. Brain and Mind Centre University of Sydney Sydney New South Wales Australia

5. St Vincent's Hospital Sydney Sydney New South Wales Australia

6. School of Clinical Medicine, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia

7. Faculty of Medicine and Health University of Sydney Sydney New South Wales Australia

8. Royal Prince Alfred Hospital Sydney New South Wales Australia

9. Faculty of Medicine and Human Health Sciences Macquarie University Sydney New South Wales Australia

Abstract

AbstractPoint‐of‐collection testing (POCT) devices are widely used in roadside and workplace drug testing to identify recent cannabis use by measuring the presence of Δ9‐tetrahydrocannabinol (THC) in oral fluid (OF). However, the performance of POCT devices with oral medicinal cannabis products remains poorly described. In a randomised, double‐blinded, crossover trial, adults with insomnia disorder (n = 20) received a single (2 mL) oral dose of oil containing 10 mg THC + 200 mg cannabidiol, or placebo, prior to sleep. Participants were tested with the Securetec DrugWipe® 5S (10 ng/mL THC cut‐off) and Dräger DrugTest® 5000 (25 ng/mL THC cut‐off) POCT devices at baseline (pre‐treatment) and then at 0.5, 10, and 18 h post‐treatment. An OF sample, taken at each time point, was also analysed using liquid chromatography–tandem mass spectrometry. Large individual variability in OF THC concentrations was observed 0.5 h post‐treatment (range: 0–425 ng/mL; mean (SD) 48.7 (107.5) ng/mL). Both the Securetec DrugWipe® 5S and DrugTest® 5000 demonstrated poor sensitivity to THC at 0.5 h post‐treatment (25% and 50%, respectively). At 10 and 18 h post‐treatment, all participant OF THC concentrations were below screening cut‐offs, and all test results were negative. These findings highlight the relatively poor sensitivity of both devices in detecting recent use of an oral medicinal cannabis product. They also suggest a low probability of obtaining a positive THC result the morning after (‘one‐off’) use. Further research is required to establish the probability of obtaining a positive THC result with regular medicinal cannabis use.

Publisher

Wiley

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