Gu Meng, Li Anning, Mak Wenyao, Dong Fang, Xu Nuo, Zhang Jingye, Shi Yufei, Zheng Nan, Tang Zhijia, He Qingfeng, Ruan Canjun, Guo Wei, Xiang Xiaoqiang, Wang Chuanyue, Han Bing, Zhu Xiao
Department of Clinical Pharmacy and Pharmacy Administration, School of Pharmacy, Fudan University, Shanghai, China.
Department of Pharmacy, Minhang Hospital, Fudan University, Shanghai, China.
Front Pharmacol. 2023 Jan 19;14:1089862. doi: 10.3389/fphar.2023.1089862. eCollection 2023.
The sublingual combination of buprenorphine (BUP) and naloxone (NLX) is a new treatment option for opioid use disorder (OUD) and is effective in preventing drug abuse. This study aimed to explore rational dosing regimen for OUD patients in China a model-based dose optimization approach. BUP, norbuprenorphine (norBUP), and NLX plasma concentrations of 34 healthy volunteers and 12 OUD subjects after single or repeated dosing were included. A parent-metabolite population pharmacokinetics (popPK) model with transit compartments for absorption was implemented to describe the pharmacokinetic profile of BUP-norBUP. In addition, NLX concentrations were well captured by a one-compartment popPK model. Covariate analysis showed that every additional swallow after the administration within the observed range (0-12) resulted in a 3.5% reduction in BUP bioavailability. This provides a possible reason for the less-than-dose proportionality of BUP. There were no differences in the pharmacokinetic characteristics between BUP or NLX in healthy volunteers and OUD subjects. Ethnic sensitivity analysis demonstrated that the dose-normalized peak concentration and area-under-the-curve of BUP in Chinese were about half of Puerto Ricans, which was consistent with a higher clearance observed in Chinese (166 vs. 270 ). Furthermore, Monte Carlo simulations showed that an 8 mg three-times daily dose was the optimized regimen for Chinese OUD subjects. This regimen ensured that opioid receptor occupancy remained at a maximum (70%) in more than 95% of subjects, at the same time, with NLX plasma concentrations below the withdrawal reaction threshold (4.6 ).
丁丙诺啡(BUP)和纳洛酮(NLX)舌下联合用药是治疗阿片类物质使用障碍(OUD)的一种新选择,且在预防药物滥用方面有效。本研究旨在采用基于模型的剂量优化方法探索中国OUD患者的合理给药方案。纳入了34名健康志愿者和12名OUD受试者单次或重复给药后的BUP、去甲丁丙诺啡(norBUP)和NLX血浆浓度。实施了带有吸收转运室的母体-代谢产物群体药代动力学(popPK)模型来描述BUP-norBUP的药代动力学特征。此外,单室popPK模型能很好地描述NLX浓度。协变量分析表明,在观察范围内(0 - 12次)给药后每多吞咽一次,BUP生物利用度降低3.5%。这为BUP剂量不成比例提供了一个可能原因。健康志愿者和OUD受试者在BUP或NLX的药代动力学特征上没有差异。种族敏感性分析表明,中国人BUP的剂量标准化峰值浓度和曲线下面积约为波多黎各人的一半,这与中国人中观察到的较高清除率一致(166 vs. 270)。此外,蒙特卡洛模拟表明,每日三次8毫克的剂量是中国OUD受试者的优化给药方案。该方案确保在超过95%的受试者中阿片受体占有率保持在最高水平(70%),同时,NLX血浆浓度低于戒断反应阈值(4.6 )。