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An Analytical Solution for Saturable Absorption in Pharmacokinetics Models
OBJECTIVE: The first-order absorption is a common model used in Pharmacokinetics. The absorption of some drugs follows carrier mediated transport. It has been proposed that the amount of drug available may saturate the transport mechanism resulting in an absorption slower than the one predicted by t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944386/ https://www.ncbi.nlm.nih.gov/pubmed/36543972 http://dx.doi.org/10.1007/s11095-022-03455-z |
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author | Sorzano, C.O.S. Moreno, M.A. Perez-de-la-Cruz Vilas, J.L. |
author_facet | Sorzano, C.O.S. Moreno, M.A. Perez-de-la-Cruz Vilas, J.L. |
author_sort | Sorzano, C.O.S. |
collection | PubMed |
description | OBJECTIVE: The first-order absorption is a common model used in Pharmacokinetics. The absorption of some drugs follows carrier mediated transport. It has been proposed that the amount of drug available may saturate the transport mechanism resulting in an absorption slower than the one predicted by the first-order model. Saturable absorption has been modeled at the differential equation level by substituting the constant rate absorption by a Hill kinetics absorption. However, its exact solution is so far unknown. The goal of this is to know the exact solution of different Hill kinetic absorption models. METHODS: We start defining different absorption models and increasing then their complexity. The simplest case is the first-order absorption model and the most complex will be a generalized Hill kinetic absorption model. The differential equation of each model is integrated. RESULTS: The complexity of the models their solutions may be not expressed in a close-form, or in term of elementary functions. We obtain and discuss the exact solutions of the different Hill kinetics absorption models. To do that, the solutions are studied according to the possible values of the free parameters of the models. We show the differences between models through simulations. CONCLUSIONS: The knowledge of closed-form solutions allows to illustrate the differences between the different absorption models and minimizes the errors of numerical integration. |
format | Online Article Text |
id | pubmed-9944386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-99443862023-02-23 An Analytical Solution for Saturable Absorption in Pharmacokinetics Models Sorzano, C.O.S. Moreno, M.A. Perez-de-la-Cruz Vilas, J.L. Pharm Res Original Research Article OBJECTIVE: The first-order absorption is a common model used in Pharmacokinetics. The absorption of some drugs follows carrier mediated transport. It has been proposed that the amount of drug available may saturate the transport mechanism resulting in an absorption slower than the one predicted by the first-order model. Saturable absorption has been modeled at the differential equation level by substituting the constant rate absorption by a Hill kinetics absorption. However, its exact solution is so far unknown. The goal of this is to know the exact solution of different Hill kinetic absorption models. METHODS: We start defining different absorption models and increasing then their complexity. The simplest case is the first-order absorption model and the most complex will be a generalized Hill kinetic absorption model. The differential equation of each model is integrated. RESULTS: The complexity of the models their solutions may be not expressed in a close-form, or in term of elementary functions. We obtain and discuss the exact solutions of the different Hill kinetics absorption models. To do that, the solutions are studied according to the possible values of the free parameters of the models. We show the differences between models through simulations. CONCLUSIONS: The knowledge of closed-form solutions allows to illustrate the differences between the different absorption models and minimizes the errors of numerical integration. Springer US 2022-12-21 2023 /pmc/articles/PMC9944386/ /pubmed/36543972 http://dx.doi.org/10.1007/s11095-022-03455-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Research Article Sorzano, C.O.S. Moreno, M.A. Perez-de-la-Cruz Vilas, J.L. An Analytical Solution for Saturable Absorption in Pharmacokinetics Models |
title | An Analytical Solution for Saturable Absorption in Pharmacokinetics Models |
title_full | An Analytical Solution for Saturable Absorption in Pharmacokinetics Models |
title_fullStr | An Analytical Solution for Saturable Absorption in Pharmacokinetics Models |
title_full_unstemmed | An Analytical Solution for Saturable Absorption in Pharmacokinetics Models |
title_short | An Analytical Solution for Saturable Absorption in Pharmacokinetics Models |
title_sort | analytical solution for saturable absorption in pharmacokinetics models |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944386/ https://www.ncbi.nlm.nih.gov/pubmed/36543972 http://dx.doi.org/10.1007/s11095-022-03455-z |
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