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-
9-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
- 1Department of Internal Medicine VI, Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Heidelberg, Germany
- 2Institute of Legal Medicine, University of Heidelberg, Heidelberg, Germany
- 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.
Abstract
After cannabis consumption there is only limited knowledge about the pharmacokinetic (PK) and metabolic properties of 11-nor-9-carboxy-
9-tetrahydrocannabinol (CTHC), which is formed by oxidative breakdown from
9-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 (336.8
61.7
g/l) followed by a quick decline. CTHC concentration could be quantified up to 96 h after administration, with a terminal elimination half-life of 17.6
5.5 h. Total clearance was low (91.2
24.0 ml/min), with renal clearance having only a minor contribution (0.136
0.094 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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