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Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model

We extend the nonstandard finite difference method of solution to the study of pharmacokinetic–pharmacodynamic models. Pharmacokinetic (PK) models are commonly used to predict drug concentrations that drive controlled intravenous (I.V.) transfers (or infusion and oral transfers) while pharmacokineti...

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Detalles Bibliográficos
Autores principales: Egbelowo, Oluwaseun, Harley, Charis, Jacobs, Byron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590451/
https://www.ncbi.nlm.nih.gov/pubmed/28952519
http://dx.doi.org/10.3390/bioengineering4020040
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author Egbelowo, Oluwaseun
Harley, Charis
Jacobs, Byron
author_facet Egbelowo, Oluwaseun
Harley, Charis
Jacobs, Byron
author_sort Egbelowo, Oluwaseun
collection PubMed
description We extend the nonstandard finite difference method of solution to the study of pharmacokinetic–pharmacodynamic models. Pharmacokinetic (PK) models are commonly used to predict drug concentrations that drive controlled intravenous (I.V.) transfers (or infusion and oral transfers) while pharmacokinetic and pharmacodynamic (PD) interaction models are used to provide predictions of drug concentrations affecting the response of these clinical drugs. We structure a nonstandard finite difference (NSFD) scheme for the relevant system of equations which models this pharamcokinetic process. We compare the results obtained to standard methods. The scheme is dynamically consistent and reliable in replicating complex dynamic properties of the relevant continuous models for varying step sizes. This study provides assistance in understanding the long-term behavior of the drug in the system, and validation of the efficiency of the nonstandard finite difference scheme as the method of choice.
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spelling pubmed-55904512017-09-21 Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model Egbelowo, Oluwaseun Harley, Charis Jacobs, Byron Bioengineering (Basel) Article We extend the nonstandard finite difference method of solution to the study of pharmacokinetic–pharmacodynamic models. Pharmacokinetic (PK) models are commonly used to predict drug concentrations that drive controlled intravenous (I.V.) transfers (or infusion and oral transfers) while pharmacokinetic and pharmacodynamic (PD) interaction models are used to provide predictions of drug concentrations affecting the response of these clinical drugs. We structure a nonstandard finite difference (NSFD) scheme for the relevant system of equations which models this pharamcokinetic process. We compare the results obtained to standard methods. The scheme is dynamically consistent and reliable in replicating complex dynamic properties of the relevant continuous models for varying step sizes. This study provides assistance in understanding the long-term behavior of the drug in the system, and validation of the efficiency of the nonstandard finite difference scheme as the method of choice. MDPI 2017-05-04 /pmc/articles/PMC5590451/ /pubmed/28952519 http://dx.doi.org/10.3390/bioengineering4020040 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Egbelowo, Oluwaseun
Harley, Charis
Jacobs, Byron
Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model
title Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model
title_full Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model
title_fullStr Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model
title_full_unstemmed Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model
title_short Nonstandard Finite Difference Method Applied to a Linear Pharmacokinetics Model
title_sort nonstandard finite difference method applied to a linear pharmacokinetics model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590451/
https://www.ncbi.nlm.nih.gov/pubmed/28952519
http://dx.doi.org/10.3390/bioengineering4020040
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