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Urinary Acrylonitrile Metabolite Concentrations Before and after Smoked, Vaporized, and Oral Cannabis in Frequent and Occasional Cannabis Users

Author

Listed:
  • David L. Ashley

    (Department of Population Health Sciences, School of Public Health, Georgia State University, Atlanta, GA 30303, USA)

  • Víctor R. De Jesús

    (Tobacco and Volatiles Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA)

  • Osama A. Abulseoud

    (Chemistry and Drug Metabolism Section, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA)

  • Marilyn A. Huestis

    (Institute for Emerging Health Professions, Thomas Jefferson University, Philadelphia, PA 19107, USA)

  • Daniel F. Milan

    (Robert J. Tomsich Pathology & Laboratory Medicine Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA)

  • Benjamin C. Blount

    (Tobacco and Volatiles Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA)

Abstract

Cannabis use through smoking, vaping, or ingestion is increasing, but only limited studies have investigated the resulting exposure to harmful chemicals. N-acetyl-S-(2-cyanoethyl)-L-cysteine (2CYEMA), a urinary metabolite of acrylonitrile, a possible carcinogen, is elevated in the urine of past-30-day cannabis users compared to non-cannabis users. Five frequent and five occasional cannabis users smoked and vaped cannabis on separate days; one also consumed cannabis orally. Urine samples were collected before and up to 72 h post dose and urinary 2CYEMA was quantified. We compared 2CYEMA pre-exposure levels, maximum concentration, time at maximum concentration for occasional versus frequent users following different exposure routes, and measured half-life of elimination. Smoking cannabis joints rapidly (within 10 min) increased 2CYEMA in the urine of occasional cannabis users, but not in frequent users. Urine 2CYEMA did not consistently increase following vaping or ingestion in either study group. Cigarette smokers had high pre-exposure concentrations of 2CYEMA. Following cannabis smoking, the half-lives of 2CYEMA ranged from 2.5 to 9.0 h. 2CYEMA is an effective biomarker of cannabis smoke exposure, including smoke from a single cannabis joint, however, not from vaping or when consumed orally. When using 2CYEMA to evaluate exposure in cannabis users, investigators should collect the details about tobacco smoking, route of consumption, and time since last use as possible covariates.

Suggested Citation

  • David L. Ashley & Víctor R. De Jesús & Osama A. Abulseoud & Marilyn A. Huestis & Daniel F. Milan & Benjamin C. Blount, 2020. "Urinary Acrylonitrile Metabolite Concentrations Before and after Smoked, Vaporized, and Oral Cannabis in Frequent and Occasional Cannabis Users," IJERPH, MDPI, vol. 17(18), pages 1-11, September.
  • Handle: RePEc:gam:jijerp:v:17:y:2020:i:18:p:6438-:d:408696
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