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Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone

Controlled drug delivery aims to achieve an effective drug concentration in the action site for a desired period of time, while minimizing side effects. In this contribution, biodegradable poly(3-hydroxybutyrate) films were evaluated as a reservoir platform for dexamethasone controlled release. Thes...

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Autores principales: Villegas, Mercedes, Cid, Alicia Graciela, Briones, Cintia Alejandra, Romero, Analía Irma, Pistán, Florencia Alejandra, Gonzo, Elio Emilio, Gottifredi, Juan Carlos, Bermúdez, José María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598214/
https://www.ncbi.nlm.nih.gov/pubmed/31297024
http://dx.doi.org/10.1016/j.jsps.2019.04.004
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author Villegas, Mercedes
Cid, Alicia Graciela
Briones, Cintia Alejandra
Romero, Analía Irma
Pistán, Florencia Alejandra
Gonzo, Elio Emilio
Gottifredi, Juan Carlos
Bermúdez, José María
author_facet Villegas, Mercedes
Cid, Alicia Graciela
Briones, Cintia Alejandra
Romero, Analía Irma
Pistán, Florencia Alejandra
Gonzo, Elio Emilio
Gottifredi, Juan Carlos
Bermúdez, José María
author_sort Villegas, Mercedes
collection PubMed
description Controlled drug delivery aims to achieve an effective drug concentration in the action site for a desired period of time, while minimizing side effects. In this contribution, biodegradable poly(3-hydroxybutyrate) films were evaluated as a reservoir platform for dexamethasone controlled release. These systems were morphological and physicochemically characterized. In vitro release assays were performed for five different percentages of drug in the films and data were fitted by a mathematical model developed and validated by our research group. When the profiles were normalized, a single curve properly fitted all the experimental data. Using this unique curve, the dissolution efficiency (DE), the time to release a given amount of drug (t(X%)), and the mean dissolution time were calculated. Furthermore, the dissolution rate, the initial dissolution rate (a%) and the intrinsic dissolution rate were determined. The a% mean value was 1.968 × 10(−2)% released/min, t(80%) was about 14 days, and the DE was 59.6% at 14 days and 66.5% at 20 days. After 2 days, when approximately 40% of the drug was released, the dissolution rate decreased about 60% respect to the initial value. The poly(3-hydroxybutyrate) platforms behaved as an appropriate system to release and control the dexamethasone delivery, suggesting that they could be an alternative to improve drug therapy.
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spelling pubmed-65982142019-07-11 Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone Villegas, Mercedes Cid, Alicia Graciela Briones, Cintia Alejandra Romero, Analía Irma Pistán, Florencia Alejandra Gonzo, Elio Emilio Gottifredi, Juan Carlos Bermúdez, José María Saudi Pharm J Original Article Controlled drug delivery aims to achieve an effective drug concentration in the action site for a desired period of time, while minimizing side effects. In this contribution, biodegradable poly(3-hydroxybutyrate) films were evaluated as a reservoir platform for dexamethasone controlled release. These systems were morphological and physicochemically characterized. In vitro release assays were performed for five different percentages of drug in the films and data were fitted by a mathematical model developed and validated by our research group. When the profiles were normalized, a single curve properly fitted all the experimental data. Using this unique curve, the dissolution efficiency (DE), the time to release a given amount of drug (t(X%)), and the mean dissolution time were calculated. Furthermore, the dissolution rate, the initial dissolution rate (a%) and the intrinsic dissolution rate were determined. The a% mean value was 1.968 × 10(−2)% released/min, t(80%) was about 14 days, and the DE was 59.6% at 14 days and 66.5% at 20 days. After 2 days, when approximately 40% of the drug was released, the dissolution rate decreased about 60% respect to the initial value. The poly(3-hydroxybutyrate) platforms behaved as an appropriate system to release and control the dexamethasone delivery, suggesting that they could be an alternative to improve drug therapy. Elsevier 2019-07 2019-04-02 /pmc/articles/PMC6598214/ /pubmed/31297024 http://dx.doi.org/10.1016/j.jsps.2019.04.004 Text en © 2019 The Authors https://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 Article
Villegas, Mercedes
Cid, Alicia Graciela
Briones, Cintia Alejandra
Romero, Analía Irma
Pistán, Florencia Alejandra
Gonzo, Elio Emilio
Gottifredi, Juan Carlos
Bermúdez, José María
Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
title Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
title_full Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
title_fullStr Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
title_full_unstemmed Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
title_short Films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
title_sort films based on the biopolymer poly(3-hydroxybutyrate) as platforms for the controlled release of dexamethasone
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598214/
https://www.ncbi.nlm.nih.gov/pubmed/31297024
http://dx.doi.org/10.1016/j.jsps.2019.04.004
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