Article

Clinical Pharmacology & Therapeutics (2007) 82, 63–69. doi:10.1038/sj.clpt.6100199; published online 4 April 2007.

Pharmacokinetics of 11-nor-9-Carboxy-Delta9-Tetrahydrocannabinol (CTHC) After Intravenous Administration of CTHC in Healthy Human Subjects

A Glaz-Sandberg1, L Dietz2, H Nguyen3, H Oberwittler1, Rolf Aderjan2 and Gerd Mikus1

  1. 1Department of Internal Medicine VI, Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Heidelberg, Germany
  2. 2Institute of Legal Medicine, University of Heidelberg, Heidelberg, Germany
  3. 3University Hospital Pharmacy, Heidelberg, Germany

Correspondence: G Mikus, (gerd.mikus@med.uni-heidelberg.de)

Received 29 December 2006; Accepted 21 February 2007; Published online 4 April 2007.

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Abstract

After cannabis consumption there is only limited knowledge about the pharmacokinetic (PK) and metabolic properties of 11-nor-9-carboxy-Delta9-tetrahydrocannabinol (CTHC), which is formed by oxidative breakdown from Delta9-tetrahydrocannabinol (THC). Despite widely-varying concentrations observed in smoking studies, attempts have been made to interpret consumption behavior with special regard to a cumulated or decreasing concentration of CTHC in serum. Ten healthy nonsmoking white male individuals received 5 mg CTHC intravenously over 10 min. Highest serum concentrations of CTHC were observed at the end of the infusion (336.8plusminus61.7 mug/l) followed by a quick decline. CTHC concentration could be quantified up to 96 h after administration, with a terminal elimination half-life of 17.6plusminus5.5 h. Total clearance was low (91.2plusminus24.0 ml/min), with renal clearance having only a minor contribution (0.136plusminus0.094 ml/min). This first metabolite-based kinetic approach will allow an advanced understanding of CTHC PKs data obtained in previous studies with THC.

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