Abstract

The use of cannabis flowering tops with standardized amounts of active phytocannabinoids was recently authorized in several countries to treat several painful pathological conditions. The acute pharmacological effects and disposition of Δ-9-tetrahydrocannabinol (THC), cannabidiol (CBD), their acidic precursors and THC metabolites after oil and decoction administration have been already described. In this study, the disposition of CBD metabolites: 7-carboxy-cannabidiol (7-COOH-CBD), 7-hydroxycannabidiol (7-OH-CBD), 6-α-hydroxycannabidiol (6-α-OH-CBD), and 6-β-hydroxycannabidiol (6-β-OH-CBD) in the serum and urine of healthy volunteers was presented. Thirteen healthy volunteers were administered 100 mL of cannabis decoction in the first experimental session and, after 15 days of washout, 0.45 mL of oil. Serum and urine samples were collected at different time points, and the CBD metabolites were quantified by ultra-high-performance liquid chromatography–tandem mass spectrometry. The most abundant serum metabolite was 7-COOH-CBD, followed by 7-OH-CBD, 6-β-OH-CBD, and6-α-OH-CBD, after decoction and oil. Both 7-OH-CBD and the 6-α-OH-CBD showed similar pharmacokinetic properties following administration of both cannabis preparations, whereas 7-COOH and 6-α-OH-CBD displayed a significant higher bioavailability after decoction consumption. All CBD metabolites were similarly excreted after oil and decoction intake apart from 6-α-OH-CBD, which had a significantly lower excretion after oil administration. The pharmacokinetic characterization of CBD metabolites is crucial for clinical practice since the cannabis herbal preparations are increasingly used for several pathological conditions.

Highlights

  • Since cannabis decoction and oil are the most used medical cannabis herbal preparations, we recently investigated the disposition of THC, CBD, their acidic precursors (∆-9-tetrahydrocannabinolic acid A-THCA-A and cannabidiolic acid—CBDA) and THC principal metabolites in the serum, oral fluid, sweat patch, and urine of healthy individuals treated with these two products [9]

  • Once CBD metabolites became commercially available, we investigated the disposition and pharmacokinetics of cannabidiol-7-oic acid (7-COOH-CBD), 7-hydroxycannabidiol (7-OH-CBD), 6-alpha-hydroxycannabidiol (6-α-OH-CBD), and 6-beta-hydroxycannabidiol (6-β-OH-CBD), in serum and urine samples stored from the previous study concerning healthy individuals treated with a single administration of cannabis decoction and cannabis oil containing similar amounts of phytocannabinoids

  • Higher amounts of THC and CBD were observed in cannabis oil and significantly higher amounts of CBDA in cannabis decoction after preparation

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Summary

Introduction

Since cannabis decoction and oil are the most used medical cannabis herbal preparations, we recently investigated the disposition of THC, CBD, their acidic precursors (∆-9-tetrahydrocannabinolic acid A-THCA-A and cannabidiolic acid—CBDA) and THC principal metabolites in the serum, oral fluid, sweat patch, and urine of healthy individuals treated with these two products [9]. It was the first time that the pharmacokinetics of phytocannabinoids present in medical cannabis was explored in healthy subjects, since two previous studies involved children and young adults with drug-resistant epilepsy [10,11] and medication-overuse headache patients [12]. Once CBD metabolites became commercially available, we investigated the disposition and pharmacokinetics of cannabidiol-7-oic acid (7-COOH-CBD), 7-hydroxycannabidiol (7-OH-CBD), 6-alpha-hydroxycannabidiol (6-α-OH-CBD), and 6-beta-hydroxycannabidiol (6-β-OH-CBD), in serum and urine samples stored from the previous study concerning healthy individuals treated with a single administration of cannabis decoction and cannabis oil containing similar amounts of phytocannabinoids

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