- Journal Home
- Volume 36 - 2024
- Volume 35 - 2024
- Volume 34 - 2023
- Volume 33 - 2023
- Volume 32 - 2022
- Volume 31 - 2022
- Volume 30 - 2021
- Volume 29 - 2021
- Volume 28 - 2020
- Volume 27 - 2020
- Volume 26 - 2019
- Volume 25 - 2019
- Volume 24 - 2018
- Volume 23 - 2018
- Volume 22 - 2017
- Volume 21 - 2017
- Volume 20 - 2016
- Volume 19 - 2016
- Volume 18 - 2015
- Volume 17 - 2015
- Volume 16 - 2014
- Volume 15 - 2014
- Volume 14 - 2013
- Volume 13 - 2013
- Volume 12 - 2012
- Volume 11 - 2012
- Volume 10 - 2011
- Volume 9 - 2011
- Volume 8 - 2010
- Volume 7 - 2010
- Volume 6 - 2009
- Volume 5 - 2009
- Volume 4 - 2008
- Volume 3 - 2008
- Volume 2 - 2007
- Volume 1 - 2006
Cited by
- BibTex
- RIS
- TXT
We discuss the basic concept of compartmental modelling in pharmacokinetics and demonstrate that all the solutions admitted by multi-compartment models of classical pharmacokinetics are expressed as linear combinations of exponential functions of time. This lends itself to data analysis that depends on fitting exponential functions to finite size sets. A mathematical method developed a long time ago to deal with this type of problem is called Prony's method. We discuss the usefulness of this method in pharmacokinetic modeling and apply it to a particular data set obtained for the drug mibefradil. In spite of the method's power in dealing with well-behaved data sets, we indicate the existence of severe limitations since real concentration curves coming from pharmacokinetic data are seldom purely exponential.
}, issn = {1991-7120}, doi = {https://doi.org/}, url = {http://global-sci.org/intro/article_detail/cicp/7897.html} }We discuss the basic concept of compartmental modelling in pharmacokinetics and demonstrate that all the solutions admitted by multi-compartment models of classical pharmacokinetics are expressed as linear combinations of exponential functions of time. This lends itself to data analysis that depends on fitting exponential functions to finite size sets. A mathematical method developed a long time ago to deal with this type of problem is called Prony's method. We discuss the usefulness of this method in pharmacokinetic modeling and apply it to a particular data set obtained for the drug mibefradil. In spite of the method's power in dealing with well-behaved data sets, we indicate the existence of severe limitations since real concentration curves coming from pharmacokinetic data are seldom purely exponential.