Placental disposition of cannabidiol: An ex vivo perfusion study

Author:

Berman Erez1ORCID,Erenburg Natalia1ORCID,Beloosesky Ron2,Eyal Sara13ORCID,Kovo Michal4ORCID

Affiliation:

1. Institute for Drug Research, School of Pharmacy Hebrew University of Jerusalem Jerusalem Israel

2. Department of Obstetrics and Gynecology Rambam Health Care Campus Haifa Israel

3. Multidisciplinary Center for Cannabinoid Research Hebrew University of Jerusalem Jerusalem Israel

4. Department of Obstetrics and Gynecology, Meir Medical Center, Kfar Saba, and Sackler School of Medicine Tel Aviv University Tel Aviv Israel

Abstract

AbstractObjectiveIn the absence of safety data in humans, the use of cannabidiol (CBD) is not recommended during pregnancy. Yet >50% of pregnancies in women with epilepsy are unintended, making fetal exposure to CBD possible. As a small‐molecule, highly lipid‐soluble drug, CBD is likely to be distributed into the placenta and cross it. To estimate the placental distribution profile of CBD and its potential short‐term placental effects, we conducted an ex vivo perfusion study in human placentas.MethodsPlacentas were obtained from healthy women undergoing cesarean deliveries. Selected cotyledons were cannulated and perfused for 180 min with a CBD‐containing medium (250 ng/mL, .796 μmol·L−1; representative of a low therapeutic concentration; n = 8). CBD concentrations were determined at 180 min in the medium and placental tissue using liquid chromatography–tandem mass spectrometry. A customized gene panel array was used to analyze the expression of selected genes in the perfused placental cotyledons as well as in placentas perfused with 1000 ng/mL CBD (3.18 μmol·L−1; high therapeutic concentration; n = 8) and in those exposed to the vehicle.ResultsCBD was sequestered in the placental tissue, exhibiting significant variability across samples (median = 5342 ng/g tissue, range = 1066–9351 ng/g tissue). CBD concentrations in the fetal compartment were one fifth of those measured in the maternal compartment (median = 59 ng/mL, range = 48–72 ng/mL vs. 280 = ng/mL, range = 159–388 ng/mL, respectively; p < .01). Placental gene expression was not significantly altered by CBD.SignificanceThe placenta acts as a depot compartment for CBD, slowing down its distribution to the fetus. This phenomenon might yield flatter but prolonged fetal CBD levels in vivo. The attenuated transplacental CBD transfer does not imply that its use by pregnant women is safe for the fetus. Only pregnancy registries and neurocognitive assessments would establish the risk of being antenatally exposed to CBD.

Funder

Israel Science Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference45 articles.

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2. NICE.Cannabis‐based medicinal products. NICE guideline [NG144]. [Published 2019 Nov 11

3. Last updated 2021 March 2021 22]. Available from:https://www.nice.org.uk/guidance/ng144/chapter/recommendations

4. Predictors of unintended pregnancy in women with epilepsy

5. Unintended pregnancy, prenatal care, newborn outcomes, and breastfeeding in women with epilepsy

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