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Parameter estimation for physiologically based pharmacokinetics model using Bayesian inference

Authors
Kim, D.S.Sung, J.H.Lee, J.M.
Issue Date
2013
Publisher
IFAC Secretariat
Keywords
Bayesian inference; Drug delivery system; Maximum a posteriori method; MCMC simulation; PBPK model; Tegafur
Citation
IFAC Proceedings Volumes (IFAC-PapersOnline), v.10, no.PART 1, pp.637 - 642
Journal Title
IFAC Proceedings Volumes (IFAC-PapersOnline)
Volume
10
Number
PART 1
Start Page
637
End Page
642
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/17233
DOI
10.3182/20131218-3-IN-2045.00064
ISSN
1474-6670
Abstract
Physiologically based pharmacokinetics(PBPK) model can predict absorption, degradation, execration and other metabolism in drug delivery system. Thus it can be useful for regulating dose and estimating drug concentration at a particular time during the clinical demonstration. PBPK model is expressed as a set of differential equation with various parameters. Bio-chip experimental data are often noisy and sparse. This makes it difficult to estimate parameters with conventional least squares approaches. The resulting parameters often have a large confidence region. This work presents a Bayesian inference algorithm with an objective function suitable for PBPK model. A Markove Chain Monte Carlo(MCMC) method is employed to estimate the posterior distribution of the parameters. We illustrate the approach with a Tegafur delivery system. © IFAC.
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