Pharmacokinetics and Bioavailability of Cannabinoids Administered via a Novel Orobuccal Nanoparticle Formulation (NanoCelle™) in Patients with Advanced Cancer.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Stephanie E Reuter, Hayley B Schultz, Andrew J McLachlan, Jeremy D Henson, Luis Vitetta
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Abstract

Introduction: The administration of cannabinoids for disease and symptom management such as pain continues to elicit significant interest, albeit limited information that is available regarding their pharmacokinetics and pharmacodynamics to guide clinical practice. Cannabis-based medicines contain a wide variety of chemical compounds, of which the most common include the cannabinoids delta-9-tetrahydrocannabinol (Δ9THC), and the nonpsychomimetic cannabidiol (CBD). The pharmacokinetics of cannabis-based medicines and the effects observed depend on the formulation and route of administration. THC and CBD are subject to extensive first-pass hepatic metabolism and pharmacokinetic drug interactions, the latter via inhibition or induction of enzymes and transporters. This study was conducted to describe the pharmacokinetics of CBD, THC, and its metabolites following orobuccal administration, providing pivotal information to guide the clinical development program of a self-assembled micellized nanoparticle formulation containing 1:1 Δ9THC and CBD. Methods: Pharmacokinetic data was obtained from a phase 1, two-stage study in patients with advanced cancer, and modelled using a population pharmacokinetic approach. To provide an indication of predicted exposure with multiple dosing, the final population pharmacokinetic models were used to simulate concentration-time profiles for each of the active compounds. Results: The developed population pharmacokinetic models provided important information on the bioavailability of CBD and THC, with estimated values of 10% and 27%, respectively. These values were approximately two-fold greater than that which has been previously described for oromucosal formulations. Discussion: This enhanced bioavailability can most likely be attributed to the NanoCelle® technology. This technology provides evidence to support the application of this innovative drug delivery platform to overcome limitations associated with cannabinoid administration for therapeutic use.

晚期癌症患者通过新型口腔纳米颗粒制剂(NanoCelle™)给予大麻素的药代动力学和生物利用度。
大麻素用于疾病和症状管理(如疼痛)继续引起人们的极大兴趣,尽管关于其药代动力学和药效学的可用信息有限,以指导临床实践。以大麻为基础的药物含有多种化合物,其中最常见的包括大麻素δ -9-四氢大麻酚(Δ9THC)和非拟精神大麻二酚(CBD)。以大麻为基础的药物的药代动力学和观察到的效果取决于制剂和给药途径。四氢大麻酚和CBD受到广泛的首过肝脏代谢和药代动力学药物相互作用的影响,后者通过抑制或诱导酶和转运体。本研究旨在描述口服给药后CBD、四氢大麻酚及其代谢物的药代动力学,为指导含有1:1 Δ9THC和CBD的自组装胶束纳米颗粒制剂的临床开发计划提供关键信息。方法:药代动力学数据来自一项针对晚期癌症患者的一期两期研究,并采用群体药代动力学方法建模。为了提供多剂量预测暴露的指示,最终群体药代动力学模型用于模拟每种活性化合物的浓度-时间分布。结果:建立的群体药代动力学模型提供了CBD和THC生物利用度的重要信息,估计值分别为10%和27%。这些值大约比先前描述的粘膜制剂的值大两倍。讨论:这种增强的生物利用度很可能归功于NanoCelle®技术。这项技术为支持这种创新药物输送平台的应用提供了证据,以克服与大麻素治疗使用相关的限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cannabis and Cannabinoid Research
Cannabis and Cannabinoid Research PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
7.90%
发文量
164
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