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Pharmacokinetics of cannabidiol administered by 3 delivery methods at 2 different dosages to healthy dogs

机译:通过3种递送方法以2种不同剂量向健康犬给药的大麻二酚的药代动力学

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摘要

The purpose of this study was to determine the pharmacokinetics of cannabidiol (CBD) in healthy dogs. Thirty, healthy research dogs were assigned to receive 1 of 3 formulations (oral microencapsulated oil beads, oral CBD-infused oil, or CBD-infused transdermal cream), at a dose of 75 mg or 150 mg q12h for 6 wk. Serial cannabidiol plasma concentrations were measured over the first 12 h and repeated at 2, 4, and 6 wk. Higher systemic exposures were observed with the oral CBD-infused oil formulation and the half-life after a 75-mg and 150-mg dose was 199.7 ± 55.9 and 127.5 ± 32.2 min, respectively. Exposure is dose-proportional and the oral CBD-infused oil provides the most favorable pharmacokinetic profile.
机译:这项研究的目的是确定大麻素(CBD)在健康犬中的药代动力学。 30只健康的研究犬被分配接受3种配方中的一种(口服微囊化油珠,口服CBD注入油或CBD注入透皮乳膏),剂量为75 mg或150 mg q12h,持续6周。在最初的12小时内测量了连续的大麻二酚血浆浓度,并在2、4和6周重复进行。口服CBD的油制剂观察到较高的全身暴露,在75 mg和150 mg剂量下的半衰期分别为199.7±55.9和127.5±32.2 min。暴露与剂量成正比,口服CBD注入的油提供最有利的药代动力学特征。

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