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

IF 6.6 1区 医学 Q1 CLINICAL NEUROLOGY Epilepsia Pub Date : 2025-01-13 DOI:10.1111/epi.18255
Lucas Brstilo, Gabriela Reyes Valenzuela, Manuel Ibarra, Paulo Cáceres Guido, Ignacio Bressan, Nora Marin, Sandra Fabiana Delaven, Silvana Agostini, Carlos Pérez Montilla, María Emilia López, Araceli Cresta, Marisa Armeno, Facundo García Bournissen, Roberto Caraballo, Paula Schaiquevich
{"title":"Population pharmacokinetics of cannabidiol and the impact of food and formulation on systemic exposure in children with drug-resistant developmental and epileptic encephalopathies.","authors":"Lucas Brstilo, Gabriela Reyes Valenzuela, Manuel Ibarra, Paulo Cáceres Guido, Ignacio Bressan, Nora Marin, Sandra Fabiana Delaven, Silvana Agostini, Carlos Pérez Montilla, María Emilia López, Araceli Cresta, Marisa Armeno, Facundo García Bournissen, Roberto Caraballo, Paula Schaiquevich","doi":"10.1111/epi.18255","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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<sub>max</sub>) and area under the concentration-time curve between 0 and 12 h (AUC<sub>0-12</sub>) were calculated.</p><p><strong>Results: </strong>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<sub>max</sub> increased by 41% and AUC<sub>0-12</sub> by 45% when CBD was administered with food compared to fasting. Dose-normalized AUC<sub>0-12</sub> was approximately 50% lower with CBD-enriched oil compared to purified CBD.</p><p><strong>Significance: </strong>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.</p>","PeriodicalId":11768,"journal":{"name":"Epilepsia","volume":" ","pages":""},"PeriodicalIF":6.6000,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epilepsia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/epi.18255","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

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 (Cmax) and area under the concentration-time curve between 0 and 12 h (AUC0-12) 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 Cmax increased by 41% and AUC0-12 by 45% when CBD was administered with food compared to fasting. Dose-normalized AUC0-12 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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
大麻二酚的人群药代动力学以及食物和配方对耐药发育性和癫痫性脑病儿童全身暴露的影响。
目的:探讨影响大麻二酚(CBD)暴露的因素,优化其治疗效果和安全性。我们的目的是描述CBD在耐药发育性和癫痫性脑病(dee)患儿中的群体药代动力学,并评估环境、药理学和临床特征对CBD全身暴露的影响。方法:纳入2-18岁dei患者的2项药代动力学研究数据(N = 48例)。在维持治疗期间,在早晨给药之前和之后,以及在一剂纯化的CBD油制剂后长达6小时,有或没有正常热量的早餐,收集了一系列血液样本。CBD血浆浓度也可在给予CBD富集制剂后获得。样品采用有效的液相色谱/串联质谱法进行定量分析。采用非线性混合效应模型建立CBD群体药代动力学模型。评估了制剂、伴随食物摄入、人口统计学、临床和药理学因素对CBD药代动力学的影响。计算模拟最大血浆浓度(Cmax)和0 ~ 12 h浓度-时间曲线下面积(AUC0-12)。结果:具有转运区和一阶消除的单室模型最能描述CBD的药代动力学。CBD表观清除率(CL/F)和分布容积(V/F)平均值分别为143.5 L/h和1892.4 L。体重对V/F和CL/F进行异速测量,性别与V/F相关,配方和食物条件与F(相对生物利用度)相关。与禁食相比,与食物一起服用CBD时,CBD Cmax增加了41%,AUC0-12增加了45%。与纯化的CBD相比,富含CBD的油的剂量标准化AUC0-12约低50%。意义:在本研究中,我们描述了食物和配方对迪斯儿童CBD暴露的影响。CBD暴露出现重大变化的食物摄取和增加药物暴露CBD配方之间切换时应考虑病人的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Epilepsia
Epilepsia 医学-临床神经学
CiteScore
10.90
自引率
10.70%
发文量
319
审稿时长
2-4 weeks
期刊介绍: Epilepsia is the leading, authoritative source for innovative clinical and basic science research for all aspects of epilepsy and seizures. In addition, Epilepsia publishes critical reviews, opinion pieces, and guidelines that foster understanding and aim to improve the diagnosis and treatment of people with seizures and epilepsy.
期刊最新文献
Vagus nerve stimulation in Lennox-Gastaut syndrome: Twenty-four-month data and experience from the CORE-VNS study. Neural mass modeling reveals that hyperexcitability underpins slow-wave sleep changes in children with epilepsy. The role of electroencephalography in epilepsy research-From seizures to interictal activity and comorbidities. Risk of epilepsy following first unprovoked and acute seizures: Cohort study. Evolution in the prescription and cost of non-intravenous rescue benzodiazepines for the treatment of seizure emergencies.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1