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Fractal Kinetic Implementation in Population Pharmacokinetic Modeling

Compartment modeling is a widely accepted technique in the field of pharmacokinetic analysis. However, conventional compartment modeling is performed under a homogeneity assumption that is not a naturally occurring condition. Since the assumption lacks physiological considerations, the respective mo...

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Autores principales: Jung, Woojin, Ryu, Hyo-jeong, Chae, Jung-woo, Yun, Hwi-yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867137/
https://www.ncbi.nlm.nih.gov/pubmed/36678932
http://dx.doi.org/10.3390/pharmaceutics15010304
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author Jung, Woojin
Ryu, Hyo-jeong
Chae, Jung-woo
Yun, Hwi-yeol
author_facet Jung, Woojin
Ryu, Hyo-jeong
Chae, Jung-woo
Yun, Hwi-yeol
author_sort Jung, Woojin
collection PubMed
description Compartment modeling is a widely accepted technique in the field of pharmacokinetic analysis. However, conventional compartment modeling is performed under a homogeneity assumption that is not a naturally occurring condition. Since the assumption lacks physiological considerations, the respective modeling approach has been questioned, as novel drugs are increasingly characterized by physiological or physical features. Alternative approaches have focused on fractal kinetics, but evaluations of their application are lacking. Thus, in this study, a simulation was performed to identify desirable fractal-kinetics applications in conventional modeling. Visible changes in the profiles were then investigated. Five cases of finalized population models were collected for implementation. For model diagnosis, the objective function value (OFV), Akaike’s information criterion (AIC), and corrected Akaike’s information criterion (AICc) were used as performance metrics, and the goodness of fit (GOF), visual predictive check (VPC), and normalized prediction distribution error (NPDE) were used as visual diagnostics. In most cases, model performance was enhanced by the fractal rate, as shown in a simulation study. The necessary parameters of the fractal rate in the model varied and were successfully estimated between 0 and 1. GOF, VPC, and NPDE diagnostics show that models with the fractal rate described the data well and were robust. In the simulation study, the fractal absorption process was, therefore, chosen for testing. In the estimation study, the rate application yielded improved performance and good prediction–observation agreement in early sampling points, and did not cause a large shift in the original estimation results. Thus, the fractal rate yielded explainable parameters by setting only the heterogeneity exponent, which reflects true physiological behavior well. This approach can be expected to provide useful insights in pharmacological decision making.
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spelling pubmed-98671372023-01-22 Fractal Kinetic Implementation in Population Pharmacokinetic Modeling Jung, Woojin Ryu, Hyo-jeong Chae, Jung-woo Yun, Hwi-yeol Pharmaceutics Article Compartment modeling is a widely accepted technique in the field of pharmacokinetic analysis. However, conventional compartment modeling is performed under a homogeneity assumption that is not a naturally occurring condition. Since the assumption lacks physiological considerations, the respective modeling approach has been questioned, as novel drugs are increasingly characterized by physiological or physical features. Alternative approaches have focused on fractal kinetics, but evaluations of their application are lacking. Thus, in this study, a simulation was performed to identify desirable fractal-kinetics applications in conventional modeling. Visible changes in the profiles were then investigated. Five cases of finalized population models were collected for implementation. For model diagnosis, the objective function value (OFV), Akaike’s information criterion (AIC), and corrected Akaike’s information criterion (AICc) were used as performance metrics, and the goodness of fit (GOF), visual predictive check (VPC), and normalized prediction distribution error (NPDE) were used as visual diagnostics. In most cases, model performance was enhanced by the fractal rate, as shown in a simulation study. The necessary parameters of the fractal rate in the model varied and were successfully estimated between 0 and 1. GOF, VPC, and NPDE diagnostics show that models with the fractal rate described the data well and were robust. In the simulation study, the fractal absorption process was, therefore, chosen for testing. In the estimation study, the rate application yielded improved performance and good prediction–observation agreement in early sampling points, and did not cause a large shift in the original estimation results. Thus, the fractal rate yielded explainable parameters by setting only the heterogeneity exponent, which reflects true physiological behavior well. This approach can be expected to provide useful insights in pharmacological decision making. MDPI 2023-01-16 /pmc/articles/PMC9867137/ /pubmed/36678932 http://dx.doi.org/10.3390/pharmaceutics15010304 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jung, Woojin
Ryu, Hyo-jeong
Chae, Jung-woo
Yun, Hwi-yeol
Fractal Kinetic Implementation in Population Pharmacokinetic Modeling
title Fractal Kinetic Implementation in Population Pharmacokinetic Modeling
title_full Fractal Kinetic Implementation in Population Pharmacokinetic Modeling
title_fullStr Fractal Kinetic Implementation in Population Pharmacokinetic Modeling
title_full_unstemmed Fractal Kinetic Implementation in Population Pharmacokinetic Modeling
title_short Fractal Kinetic Implementation in Population Pharmacokinetic Modeling
title_sort fractal kinetic implementation in population pharmacokinetic modeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867137/
https://www.ncbi.nlm.nih.gov/pubmed/36678932
http://dx.doi.org/10.3390/pharmaceutics15010304
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