National Centre for Sport and Exercise Medicine, School of Sport, Health and Exercise Sciences, Loughborough University, Loughborough, Leicestershire, United Kingdom.
Cannabis Cannabinoid Res. 2024 Oct;9(5):e1423-e1432. doi: 10.1089/can.2023.0117. Epub 2023 Sep 22.
Cannabidiol (CBD) is a nonintoxicating phytocannabinoid used in clinical treatments and sold widely in consumer products. CBD products may be designed for sublingual or oral delivery, but it is unclear whether either is advantageous for CBD absorption. This study compared CBD pharmacokinetics after providing CBD oil as sublingual drops and within orally ingested gelatin capsules, at a dose relevant to consumer products. Eight males completed three conditions in a participant-blinded, randomized crossover design. Participants received the following combinations of placebo and CBD-containing (69 mg/mL) hemp oil in capsules and as sublingual drops: placebo capsules/placebo drops (), CBD capsules/placebo drops (), and placebo capsules/CBD drops (). Blood samples, blood pressure, and subjective scales were obtained/completed hourly for 6 h and at 24 h. Plasma CBD concentrations were not different between and (interaction effect =0.76). Peak CBD concentration (28.0±15.6 vs. 24.0±22.2 ng/mL), time of peak CBD concentration (4±1 vs. 4±2 h), and area under the concentration curve (45.3±20.3 vs. 41.8±23.3 ng/mL·6 h) were not different between conditions (≥0.25). Cardiometabolic outcomes (plasma glucose/triacylglycerol, heart rate, blood pressure), liver function (plasma alanine aminotransferase/aspartate aminotransferase), kidney function (plasma creatinine), and subjective feelings/symptoms were not different between conditions (≥0.07). Plasma CBD profiles were comparable between and , suggesting that there were not meaningful differences in routes of CBD absorption between conditions. This implies that CBD oil delivered sublingually is swallowed before oral mucosal CBD absorption occurs, which may have implications for research design, CBD product design, and consumer product choice.
大麻二酚(CBD)是一种非成瘾性植物大麻素,用于临床治疗,并广泛销售于消费产品。CBD 产品可能设计用于舌下或口服给药,但尚不清楚这两种途径哪种更有利于 CBD 的吸收。本研究在与消费产品相关的剂量下,比较了舌下滴注 CBD 油和口服摄入含 CBD 的明胶胶囊后的 CBD 药代动力学。8 名男性以参与者盲法、随机交叉设计完成了三项条件。参与者接受了以下三种组合的安慰剂和含 CBD(69mg/mL)的大麻油胶囊和舌下滴剂:安慰剂胶囊/安慰剂滴剂()、CBD 胶囊/安慰剂滴剂()和安慰剂胶囊/CBD 滴剂()。在 6 小时和 24 小时时采集了血液样本、测量了血压并完成了主观量表。血浆 CBD 浓度在 与 之间没有差异(交互作用效应=0.76)。CBD 峰值浓度(28.0±15.6 与 24.0±22.2ng/mL)、CBD 峰值浓度时间(4±1 与 4±2h)和 AUC0-6h(45.3±20.3 与 41.8±23.3ng/mL·6h)在各条件之间无差异(≥0.25)。代谢心脏结局(血浆葡萄糖/三酰甘油、心率、血压)、肝功能(血浆丙氨酸氨基转移酶/天冬氨酸氨基转移酶)、肾功能(血浆肌酐)和主观感受/症状在各条件之间无差异(≥0.07)。 与 之间的 CBD 血浆谱相似,表明两种途径的 CBD 吸收之间没有明显差异。这意味着舌下给予的 CBD 油在口腔黏膜 CBD 吸收之前被吞咽,这可能对研究设计、CBD 产品设计和消费者产品选择具有意义。