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Input estimation in nonlinear dynamical systems for drug-discovery applications.
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Trägårdh, Magnus (2017) Input estimation in nonlinear dynamical systems for drug-discovery applications. PhD thesis, University of Warwick.
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WRAP_Theses_Trägårdh_2017.pdf - Submitted Version - Requires a PDF viewer. Download (3171Kb) | Preview |
Official URL: http://webcat.warwick.ac.uk/record=b3142182~S15
Abstract
In mathematical modelling for drug discovery, nonparametric methods are an alternative to the more commonly used parametric methods, and have the advantage of requiring fewer modelling assumptions. This thesis considers nonparametric methods for performing input estimation (deconvolution) -- inferring the input to a dynamical system based on measurements of the system’s state. A typical application is to determine the absorption profile of an orally administered drug. Commonly used input-estimation methods are restricted to system models that are linear. This thesis aims to develop and evaluate methods which can be applied to nonlinear systems, and which are additionally able to provide uncertainty estimates. An input-estimation method is considered to be a particular choice of 1) prior, 2) function parameterisation, 3) desired statistical quantity, and 4) estimation algorithm. Two classes of methods have been selected and implemented: direct optimal-control methods and Markov chain Monte Carlo (MCMC) methods. These have been evaluated on two pharmacokinetic and two body-weight modelling applications, using simulated as well as real data. Evaluation was based on several criteria, including accuracy, computational speed, and usability. The results show that the methods can achieve good accuracy, provided that data are relatively densely sampled. Properly applied, optimal-control methods can achieve very high speed, approximately 0.1s for typical problems, at the expense of not providing uncertainty estimates. For MCMC methods, the performance is highly dependent on the method settings as well as on the problem. In many cases, MCMC running times can be significantly reduced by a suitable choice of function parameterisation and sampling method. In all cases, estimation is based on clearly stated, quantifiable assumptions.
Item Type: | Thesis (PhD) | ||||
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Subjects: | R Medicine > RM Therapeutics. Pharmacology | ||||
Library of Congress Subject Headings (LCSH): | Drug development -- Mathematical models, Oral medication, Markov processes, Monte Carlo method | ||||
Official Date: | May 2017 | ||||
Dates: |
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Institution: | University of Warwick | ||||
Theses Department: | School of Engineering | ||||
Thesis Type: | PhD | ||||
Publication Status: | Unpublished | ||||
Sponsors: | Seventh Framework Programme (European Commission) | ||||
Extent: | xvii, 219 leaves : charts, illustrations. | ||||
Language: | eng |
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