Modelling circadian variation in the pharmacokinetics of non-steroidal anti-inflammatory drugs.

Abstract:

:A one-compartment model with first-order absorption has provided good fits to five sets of indomethacin data and four sets of ketoprofen data taken at different times of day. There was substantial variation in the model parameters with time of administration and most of the features of this variation applied equally to both drugs. From the data examined, the source of variation appears to be mainly in the absorption phase and this was confirmed using a chronokinetic analysis, in which simultaneous fits were obtained with time-variant rate parameters. However, there may also be circadian variation in protein binding. The danger of quoting parameter values for either of these two drugs based on administration at a single time of day has been illustrated, and this may well be true for other drugs.

journal_name

Eur J Clin Pharmacol

authors

Aronson JK,Chappell MJ,Godfrey KR,Yew MK

doi

10.1007/BF00265955

subject

Has Abstract

pub_date

1993-01-01 00:00:00

pages

357-61

issue

4

eissn

0031-6970

issn

1432-1041

journal_volume

45

pub_type

杂志文章
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    更新日期:2020-11-11 00:00:00

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    pub_type: 杂志文章

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    pub_type: 杂志文章

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