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Validation of kinetic modeling of progesterone release from polymeric membranes
Mathematical modeling in drug release systems is fundamental in development and optimization of these systems, since it allows to predict drug release rates and to elucidate the physical transport mechanisms involved. In this paper we validate a novel mathematical model that describes progesterone (...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032242/ https://www.ncbi.nlm.nih.gov/pubmed/32104378 http://dx.doi.org/10.1016/j.ajps.2017.08.007 |
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author | Romero, Analia Irma Villegas, Mercedes Cid, Alicia Graciela Parentis, Mónica Liliana Gonzo, Elio Emilio Bermúdez, José María |
author_facet | Romero, Analia Irma Villegas, Mercedes Cid, Alicia Graciela Parentis, Mónica Liliana Gonzo, Elio Emilio Bermúdez, José María |
author_sort | Romero, Analia Irma |
collection | PubMed |
description | Mathematical modeling in drug release systems is fundamental in development and optimization of these systems, since it allows to predict drug release rates and to elucidate the physical transport mechanisms involved. In this paper we validate a novel mathematical model that describes progesterone (Prg) controlled release from poly-3-hydroxybutyric acid (PHB) membranes. A statistical analysis was conducted to compare the fitting of our model with six different models and the Akaike information criterion (AIC) was used to find the equation with best-fit. A simple relation between mass and drug released rate was found, which allows predicting the effect of Prg loads on the release behavior. Our proposed model was the one with minimum AIC value, and therefore it was the one that statistically fitted better the experimental data obtained for all the Prg loads tested. Furthermore, the initial release rate was calculated and therefore, the interface mass transfer coefficient estimated and the equilibrium distribution constant of Prg between the PHB and the release medium was also determined. The results lead us to conclude that our proposed model is the one which best fits the experimental data and can be successfully used to describe Prg drug release in PHB membranes. |
format | Online Article Text |
id | pubmed-7032242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-70322422020-02-26 Validation of kinetic modeling of progesterone release from polymeric membranes Romero, Analia Irma Villegas, Mercedes Cid, Alicia Graciela Parentis, Mónica Liliana Gonzo, Elio Emilio Bermúdez, José María Asian J Pharm Sci Original Research Article Mathematical modeling in drug release systems is fundamental in development and optimization of these systems, since it allows to predict drug release rates and to elucidate the physical transport mechanisms involved. In this paper we validate a novel mathematical model that describes progesterone (Prg) controlled release from poly-3-hydroxybutyric acid (PHB) membranes. A statistical analysis was conducted to compare the fitting of our model with six different models and the Akaike information criterion (AIC) was used to find the equation with best-fit. A simple relation between mass and drug released rate was found, which allows predicting the effect of Prg loads on the release behavior. Our proposed model was the one with minimum AIC value, and therefore it was the one that statistically fitted better the experimental data obtained for all the Prg loads tested. Furthermore, the initial release rate was calculated and therefore, the interface mass transfer coefficient estimated and the equilibrium distribution constant of Prg between the PHB and the release medium was also determined. The results lead us to conclude that our proposed model is the one which best fits the experimental data and can be successfully used to describe Prg drug release in PHB membranes. Shenyang Pharmaceutical University 2018-01 2017-08-18 /pmc/articles/PMC7032242/ /pubmed/32104378 http://dx.doi.org/10.1016/j.ajps.2017.08.007 Text en © 2018 Shenyang Pharmaceutical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Article Romero, Analia Irma Villegas, Mercedes Cid, Alicia Graciela Parentis, Mónica Liliana Gonzo, Elio Emilio Bermúdez, José María Validation of kinetic modeling of progesterone release from polymeric membranes |
title | Validation of kinetic modeling of progesterone release from polymeric membranes |
title_full | Validation of kinetic modeling of progesterone release from polymeric membranes |
title_fullStr | Validation of kinetic modeling of progesterone release from polymeric membranes |
title_full_unstemmed | Validation of kinetic modeling of progesterone release from polymeric membranes |
title_short | Validation of kinetic modeling of progesterone release from polymeric membranes |
title_sort | validation of kinetic modeling of progesterone release from polymeric membranes |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032242/ https://www.ncbi.nlm.nih.gov/pubmed/32104378 http://dx.doi.org/10.1016/j.ajps.2017.08.007 |
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