Genotoxicity evaluation of cannabidiol

遗传毒性 大麻酚 微核试验 微核 药理学 艾姆斯试验 化学 毒理 生物 沙门氏菌 遗传学 毒性 医学 细菌 大麻 精神科 有机化学
作者
Rayetta G. Henderson,Brian T. Welsh,Kristen R. Trexler,Marcel O. Bonn‐Miller,Timothy W. Lefever
出处
期刊:Regulatory Toxicology and Pharmacology [Elsevier BV]
卷期号:142: 105425-105425 被引量:5
标识
DOI:10.1016/j.yrtph.2023.105425
摘要

Consumer use of cannabidiol (CBD) for personal wellness purposes has garnered much public interest. However, safety-related data on CBD in the public domain are limited, including a lack of quality studies evaluating its genotoxic potential. The quality of available studies is limited due to the test material used (e.g., low CBD purity) and/or study design, leading some global regulatory agencies to highlight genotoxicity as an important data gap for CBD. To address this gap, the genotoxic potential of a pure CBD isolate was investigated in a battery of three genotoxicity assays conducted according to OECD testing guidelines. In an in vitro microbial reverse mutation assay, CBD up to 5000 μg/plate was negative in Salmonella typhimurium strains TA98, TA100, TA1535, and TA1537, and Escherichia coli strain WP2 uvrA, with and without metabolic activation. Testing in an in vitro micronucleus assay was negative in human TK6 cells up to 10-11 μg/mL, with and without metabolic activation. Finally, an in vivo micronucleus assay conducted in male and female rats was negative for genotoxicity up to 1000 mg/kg-bw/d. Bioanalysis of CBD and its primary metabolite, 7-carboxy CBD, confirmed a dose-related increase in plasma exposure. Together, these assays indicate that CBD is unlikely to pose a genotoxic hazard.
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