Appel-Dingemanse S, Lemarechal M O, Kumle A, Hubert M, Legangneux E
Department of Clinical Pharmacology, NOVARTIS Pharma AG, Basel, Switzerland.
Br J Clin Pharmacol. 1999 May;47(5):483-91. doi: 10.1046/j.1365-2125.1999.00936.x.
The purpose of the present study was to assess the pharmacokinetics of the novel selective 5-HT4 receptor agonist SDZ HTF 919 (HTF) including food effect, absolute bioavailability, interoccasion and intersubject variabilities.
In the randomized, open-label, three treatment, four period crossover study, HTF was administered to 12 young healthy male subjects as a 12 mg tablet (twice under fasted and once under fed conditions) and a 3 mg intravenous (i.v.) infusion over 40 min (fasted). Pharmacokinetic parameters were obtained by noncompartmental methods. A more comprehensive pharmacokinetic characterization was achieved by integrated modelling of oral (p.o.) and i.v. data. To describe the absorption phase a Weibull function and a classical first order input function were compared.
Noncompartmental pharmacokinetic analysis revealed a rapid absorption (tmax 1.3 h, fasted), an absolute bioavailability of 11+/-3%, a biphasic disposition phase with a terminal half-life of 11+/-5 h, a clearance of 77+/-15 l h-1, and a volume of distribution at steady state of 368+/-223 l. The coefficients of interoccasion and interindividual variability in Cmax and AUC ranged between 17 and 28%. Food intake caused a delay (tmax 2.0 h) and decrease in absorption with consequently lower systemic exposure ( approximately 5% absolute bioavailability). Integrated p.o./i.v. pharmacokinetic modelling with a Weibull input function allowed accurate description of individual profiles. Modelling of the data from the p.o. dosing improved the description of the terminal phase by inclusion of the i. v. data and additionally provided quantitative characterization of the absorption phase.
The pharmacokinetics of HTF could be well described by an integrated modelling approach for both p.o. and i.v. data. The derived model will provide guidance in the design of future studies.
本研究旨在评估新型选择性5-羟色胺4(5-HT4)受体激动剂SDZ HTF 919(HTF)的药代动力学,包括食物影响、绝对生物利用度、给药间隔和个体间差异。
在这项随机、开放标签、三治疗、四周期交叉研究中,12名年轻健康男性受试者服用12毫克片剂形式的HTF(禁食条件下两次,进食条件下一次)以及40分钟内静脉输注3毫克HTF(禁食)。通过非房室方法获得药代动力学参数。通过口服(p.o.)和静脉(i.v.)数据的整合建模实现了更全面的药代动力学特征描述。为描述吸收阶段,比较了威布尔函数和经典一级输入函数。
非房室药代动力学分析显示吸收迅速(禁食时tmax为1.3小时),绝对生物利用度为11±3%,处置阶段呈双相,终末半衰期为11±5小时,清除率为77±15升/小时,稳态分布容积为368±223升。Cmax和AUC的给药间隔和个体间变异系数在17%至28%之间。进食导致吸收延迟(tmax为2.0小时)和吸收减少,从而使全身暴露降低(绝对生物利用度约为5%)。采用威布尔输入函数的口服/静脉药代动力学整合建模能够准确描述个体曲线。通过纳入静脉数据,口服给药数据建模改善了终末阶段的描述,还提供了吸收阶段的定量特征。
口服和静脉数据的整合建模方法能够很好地描述HTF的药代动力学。所推导的模型将为未来研究的设计提供指导。