Morning versus evening dosing of ibuprofen using conventional and time-controlled release formulations

被引:35
作者
Halsas, M
Hietala, J
Veski, P
Jürjenson, H
Marvola, M
机构
[1] Univ Helsinki, Dept Pharm, Div Biopharmaceut & Pharmacokinet, FIN-00014 Helsinki, Finland
[2] Tartu State Univ, Womens Clin, EE-202400 Tartu, Estonia
[3] Tartu State Univ, Inst Pharm, EE-2400 Tartu, Estonia
关键词
ibuprofen; time-controlled release; chronopharmacokinetics; food effect; press-coated tablet; hydroxypropylmethylcellulose;
D O I
10.1016/S0378-5173(99)00250-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many functions of the human body vary considerably during a day. These variations can lead to changes in drug plasma concentrations. In the study on healthy volunteers described here it was determined whether ibuprofen plasma levels following single oral doses of immediate-release and press-coated time-controlled release tablet formulations depend on time of drug administration (08:00 or 22:00 h). The difference between morning and evening dosing of the immediate-release formulation was minimal. The results with the press-coated formulation were unexpected having regard to results of previous studies on non-steroidal anti-inflammatory analgesics. Time to peak concentration was 6 h after morning administration, 4 h after evening administration. Both the rate and extent of bioavailability of ibuprofen were lower when dosing took place at 08:00 h than when dosing took place at 22:00 h. The influence of food on the pharmacokinetic profile of an evening dose of the press-coated formulation was also studied. When tablets were administered with a meal the ratio C-max/AUC and t(max) and AUC values indicated that bioavailability was reduced. The main conclusion was that the chronopharmacokinetic behaviour of the press-coated ibuprofen tablet is related to the formulation, not the drug substance as such. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:179 / 185
页数:7
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