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Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women
Introduction: Physiologically based pharmacokinetic (PBPK) models for the absorption, disposition, metabolism and excretion (ADME) of nicotine and its major metabolite cotinine in pregnant women (p-PBPK) are rare. The aim of this short research report is to present a p-PBPK model and its simulations...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329445/ https://www.ncbi.nlm.nih.gov/pubmed/34354586 http://dx.doi.org/10.3389/fphar.2021.688597 |
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author | Amice, Basile Ho, Harvey Zhang, En Bullen, Chris |
author_facet | Amice, Basile Ho, Harvey Zhang, En Bullen, Chris |
author_sort | Amice, Basile |
collection | PubMed |
description | Introduction: Physiologically based pharmacokinetic (PBPK) models for the absorption, disposition, metabolism and excretion (ADME) of nicotine and its major metabolite cotinine in pregnant women (p-PBPK) are rare. The aim of this short research report is to present a p-PBPK model and its simulations for nicotine and cotinine clearance. Methods: The maternal-placental-fetal compartments of the p-PBPK model contain a total of 16 compartments representing major maternal and fetal organs and tissue groups. Qualitative and quantitative data of nicotine and cotinine disposition and clearance have been incorporated into pharmacokinetic parameters. Results: The p-PBPK model reproduced the higher clearance rates of nicotine and cotinine in pregnant women than non-pregnant women. Temporal profiles for their disposition in organs such as the brain were also simulated. Nicotine concentration reaches its maximum value within 2 min after an intravenous injection. Conclusion: The proposed p-PBPK model produces results consistent with available data sources. Further pharmacokinetic experiments are required to calibrate clearance parameters for individual organs, and for the fetus. |
format | Online Article Text |
id | pubmed-8329445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83294452021-08-04 Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women Amice, Basile Ho, Harvey Zhang, En Bullen, Chris Front Pharmacol Pharmacology Introduction: Physiologically based pharmacokinetic (PBPK) models for the absorption, disposition, metabolism and excretion (ADME) of nicotine and its major metabolite cotinine in pregnant women (p-PBPK) are rare. The aim of this short research report is to present a p-PBPK model and its simulations for nicotine and cotinine clearance. Methods: The maternal-placental-fetal compartments of the p-PBPK model contain a total of 16 compartments representing major maternal and fetal organs and tissue groups. Qualitative and quantitative data of nicotine and cotinine disposition and clearance have been incorporated into pharmacokinetic parameters. Results: The p-PBPK model reproduced the higher clearance rates of nicotine and cotinine in pregnant women than non-pregnant women. Temporal profiles for their disposition in organs such as the brain were also simulated. Nicotine concentration reaches its maximum value within 2 min after an intravenous injection. Conclusion: The proposed p-PBPK model produces results consistent with available data sources. Further pharmacokinetic experiments are required to calibrate clearance parameters for individual organs, and for the fetus. Frontiers Media S.A. 2021-07-20 /pmc/articles/PMC8329445/ /pubmed/34354586 http://dx.doi.org/10.3389/fphar.2021.688597 Text en Copyright © 2021 Amice, Ho, Zhang and Bullen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Amice, Basile Ho, Harvey Zhang, En Bullen, Chris Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women |
title | Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women |
title_full | Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women |
title_fullStr | Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women |
title_full_unstemmed | Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women |
title_short | Physiologically Based Pharmacokinetic Modelling for Nicotine and Cotinine Clearance in Pregnant Women |
title_sort | physiologically based pharmacokinetic modelling for nicotine and cotinine clearance in pregnant women |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329445/ https://www.ncbi.nlm.nih.gov/pubmed/34354586 http://dx.doi.org/10.3389/fphar.2021.688597 |
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