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Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems
A series of bionanocomposites composed of shark gelatin hydrogels and PLA nanoparticles featuring different nanostructures were designed to generate multifunctional drug delivery systems with tailored release rates required for personalized treatment approaches. The global conception of the systems...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9227928/ https://www.ncbi.nlm.nih.gov/pubmed/35745711 http://dx.doi.org/10.3390/pharmaceutics14061138 |
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author | Moya-Lopez, Carmen Juan, Alberto Donizeti, Murillo Valcarcel, Jesus Vazquez, José A. Solano, Eduardo Chapron, David Bourson, Patrice Bravo, Ivan Alonso-Moreno, Carlos Clemente-Casares, Pilar Gracia-Fernández, Carlos Longo, Alessandro Salloum-Abou-Jaoude, Georges Ocaña, Alberto Piñeiro, Manuel M. Hermida-Merino, Carolina Hermida-Merino, Daniel |
author_facet | Moya-Lopez, Carmen Juan, Alberto Donizeti, Murillo Valcarcel, Jesus Vazquez, José A. Solano, Eduardo Chapron, David Bourson, Patrice Bravo, Ivan Alonso-Moreno, Carlos Clemente-Casares, Pilar Gracia-Fernández, Carlos Longo, Alessandro Salloum-Abou-Jaoude, Georges Ocaña, Alberto Piñeiro, Manuel M. Hermida-Merino, Carolina Hermida-Merino, Daniel |
author_sort | Moya-Lopez, Carmen |
collection | PubMed |
description | A series of bionanocomposites composed of shark gelatin hydrogels and PLA nanoparticles featuring different nanostructures were designed to generate multifunctional drug delivery systems with tailored release rates required for personalized treatment approaches. The global conception of the systems was considered from the desired customization of the drug release while featuring the viscoelastic properties needed for their ease of storage and posterior local administration as well as their biocompatibility and cell growth capability for the successful administration at the biomolecular level. The hydrogel matrix offers the support to develop a direct thermal method to convert the typical kinetic trapped nanostructures afforded by the formulation method whilst avoiding the detrimental nanoparticle agglomeration that diminishes their therapeutic effect. The nanoparticles generated were successfully formulated with two different antitumoral compounds (doxorubicin and dasatinib) possessing different structures to prove the loading versatility of the drug delivery system. The bionanocomposites were characterized by several techniques (SEM, DLS, RAMAN, DSC, SAXS/WAXS and rheology) as well as their reversible sol–gel transition upon thermal treatment that occurs during the drug delivery system preparation and the thermal annealing step. In addition, the local applicability of the drug delivery system was assessed by the so-called “syringe test” to validate both the storage capability and its flow properties at simulated physiological conditions. Finally, the drug release profiles of the doxorubicin from both the PLA nanoparticles or the bionanocomposites were analyzed and correlated to the nanostructure of the drug delivery system. |
format | Online Article Text |
id | pubmed-9227928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92279282022-06-25 Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems Moya-Lopez, Carmen Juan, Alberto Donizeti, Murillo Valcarcel, Jesus Vazquez, José A. Solano, Eduardo Chapron, David Bourson, Patrice Bravo, Ivan Alonso-Moreno, Carlos Clemente-Casares, Pilar Gracia-Fernández, Carlos Longo, Alessandro Salloum-Abou-Jaoude, Georges Ocaña, Alberto Piñeiro, Manuel M. Hermida-Merino, Carolina Hermida-Merino, Daniel Pharmaceutics Article A series of bionanocomposites composed of shark gelatin hydrogels and PLA nanoparticles featuring different nanostructures were designed to generate multifunctional drug delivery systems with tailored release rates required for personalized treatment approaches. The global conception of the systems was considered from the desired customization of the drug release while featuring the viscoelastic properties needed for their ease of storage and posterior local administration as well as their biocompatibility and cell growth capability for the successful administration at the biomolecular level. The hydrogel matrix offers the support to develop a direct thermal method to convert the typical kinetic trapped nanostructures afforded by the formulation method whilst avoiding the detrimental nanoparticle agglomeration that diminishes their therapeutic effect. The nanoparticles generated were successfully formulated with two different antitumoral compounds (doxorubicin and dasatinib) possessing different structures to prove the loading versatility of the drug delivery system. The bionanocomposites were characterized by several techniques (SEM, DLS, RAMAN, DSC, SAXS/WAXS and rheology) as well as their reversible sol–gel transition upon thermal treatment that occurs during the drug delivery system preparation and the thermal annealing step. In addition, the local applicability of the drug delivery system was assessed by the so-called “syringe test” to validate both the storage capability and its flow properties at simulated physiological conditions. Finally, the drug release profiles of the doxorubicin from both the PLA nanoparticles or the bionanocomposites were analyzed and correlated to the nanostructure of the drug delivery system. MDPI 2022-05-27 /pmc/articles/PMC9227928/ /pubmed/35745711 http://dx.doi.org/10.3390/pharmaceutics14061138 Text en © 2022 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 Moya-Lopez, Carmen Juan, Alberto Donizeti, Murillo Valcarcel, Jesus Vazquez, José A. Solano, Eduardo Chapron, David Bourson, Patrice Bravo, Ivan Alonso-Moreno, Carlos Clemente-Casares, Pilar Gracia-Fernández, Carlos Longo, Alessandro Salloum-Abou-Jaoude, Georges Ocaña, Alberto Piñeiro, Manuel M. Hermida-Merino, Carolina Hermida-Merino, Daniel Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems |
title | Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems |
title_full | Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems |
title_fullStr | Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems |
title_full_unstemmed | Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems |
title_short | Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems |
title_sort | multifunctional pla/gelatin bionanocomposites for tailored drug delivery systems |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9227928/ https://www.ncbi.nlm.nih.gov/pubmed/35745711 http://dx.doi.org/10.3390/pharmaceutics14061138 |
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