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Population pharmacokinetics of cannabidiol and the impact of food and formulation on systemic exposure in children with drug‐resistant developmental and epileptic encephalopathies

药代动力学 大麻酚 生物利用度 人口 药理学 分配量 医学 曲线下面积 最大值 大麻 环境卫生 精神科
作者
Lucas Brstilo,Gabriela Reyes Valenzuela,Manuel Ibarra,Paulo Cáceres Guidó,Ignacio Bressán,Nasheyra Esteban Marin,Sandra Fabiana Delaven,Silvana Agostini,Carlos A. Pérez Montilla,María Emilia Román López,Araceli Cresta,Marisa Armeno,Facundo García‐Bournissen,Roberto Caraballo,Paula Schaiquevich
出处
期刊:Epilepsia [Wiley]
标识
DOI:10.1111/epi.18255
摘要

Abstract Objective Identifying factors influencing cannabidiol (CBD) exposure can optimize treatment efficacy and safety. We aimed to describe the population pharmacokinetics of CBD in children with drug‐resistant developmental and epileptic encephalopathies (DEEs) and assess the influence of environmental, pharmacological, and clinical characteristics on CBD systemic exposure. Methods Data from two pharmacokinetic studies of patients aged 2–18 years with DEEs were included ( N = 48 patients). Serial blood samples were collected during maintenance treatment, before and after the morning dose, and up to 6 h after a dose of a purified CBD oil formulation, with or without a normocaloric breakfast. CBD plasma concentrations were also available following administration of a CBD‐enriched formulation. Samples were quantified using a validated liquid chromatography/tandem mass spectrometry assay. A CBD population pharmacokinetic model was developed using nonlinear mixed‐effects modeling. The effects of formulation, concomitant food intake, and demographic, clinical, and pharmacological factors on CBD pharmacokinetics were evaluated. Simulated maximum plasma concentration (C max ) and area under the concentration–time curve between 0 and 12 h (AUC 0‐12 ) were calculated. Results A one‐compartment model with transit compartments and first‐order elimination best described CBD pharmacokinetics. Mean values for CBD apparent clearance (CL/F) and volume of distribution (V/F) were 143.5 L/h and 1892.4 L, respectively. Weight was allometrically scaled for V/F and CL/F, sex was associated with V/F, and both formulation and food condition were associated with F (relative bioavailability). CBD C max increased by 41% and AUC 0‐12 by 45% when CBD was administered with food compared to fasting. Dose‐normalized AUC 0‐12 was approximately 50% lower with CBD‐enriched oil compared to purified CBD. Significance In the present study, we described the effects of food and formulation on CBD exposure in children with DEEs. Increased CBD exposure with food intake and significant changes in drug exposure when switching between CBD formulations should be considered in patient management.
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