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Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus

The low toxicity and high adsorption capacities of clay minerals make them attractive for controlled delivery applications. However, the number of controlled-release studies in the literature using clay minerals is still scarce. In this work, three different clays from the smectite group (Kunipia F,...

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Autores principales: Poyatos-Racionero, Elisa, Pérez-Esteve, Édgar, Medaglia, Serena, Aznar, Elena, Barat, José M., Martínez-Máñez, Ramón, Marcos, Maria Dolores, Bernardos, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9370449/
https://www.ncbi.nlm.nih.gov/pubmed/35957126
http://dx.doi.org/10.3390/nano12152694
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author Poyatos-Racionero, Elisa
Pérez-Esteve, Édgar
Medaglia, Serena
Aznar, Elena
Barat, José M.
Martínez-Máñez, Ramón
Marcos, Maria Dolores
Bernardos, Andrea
author_facet Poyatos-Racionero, Elisa
Pérez-Esteve, Édgar
Medaglia, Serena
Aznar, Elena
Barat, José M.
Martínez-Máñez, Ramón
Marcos, Maria Dolores
Bernardos, Andrea
author_sort Poyatos-Racionero, Elisa
collection PubMed
description The low toxicity and high adsorption capacities of clay minerals make them attractive for controlled delivery applications. However, the number of controlled-release studies in the literature using clay minerals is still scarce. In this work, three different clays from the smectite group (Kunipia F, montmorillonite; Sumecton SA, saponite; and Sumecton SWN, hectorite) were successfully loaded with rhodamine B dye and functionalized with oleic acid as a gatekeeper to produce organonanoclays for active and controlled payload-release. Moreover, hematin and cyanocobalamin have also been encapsulated in hectorite gated clay. These organonanoclays were able to confine the entrapped cargos in an aqueous environment, and effectively release them in the presence of surfactants (as bile salts). A controlled delivery of 49 ± 6 μg hematin/mg solid and 32.7 ± 1.5 μg cyanocobalamin/mg solid was reached. The cargo release profiles of all of the organonanoclays were adjusted to three different release-kinetic models, demonstrating the Korsmeyer–Peppas model with release dependence on (i) the organic–inorganic hybrid system, and (ii) the nature of loaded molecules and their interaction with the support. Furthermore, in vitro cell viability assays were carried out with Caco-2 cells, demonstrating that the organonanoclays are well tolerated by cells at particle concentrations of ca. 50 μg/mL.
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spelling pubmed-93704492022-08-12 Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus Poyatos-Racionero, Elisa Pérez-Esteve, Édgar Medaglia, Serena Aznar, Elena Barat, José M. Martínez-Máñez, Ramón Marcos, Maria Dolores Bernardos, Andrea Nanomaterials (Basel) Article The low toxicity and high adsorption capacities of clay minerals make them attractive for controlled delivery applications. However, the number of controlled-release studies in the literature using clay minerals is still scarce. In this work, three different clays from the smectite group (Kunipia F, montmorillonite; Sumecton SA, saponite; and Sumecton SWN, hectorite) were successfully loaded with rhodamine B dye and functionalized with oleic acid as a gatekeeper to produce organonanoclays for active and controlled payload-release. Moreover, hematin and cyanocobalamin have also been encapsulated in hectorite gated clay. These organonanoclays were able to confine the entrapped cargos in an aqueous environment, and effectively release them in the presence of surfactants (as bile salts). A controlled delivery of 49 ± 6 μg hematin/mg solid and 32.7 ± 1.5 μg cyanocobalamin/mg solid was reached. The cargo release profiles of all of the organonanoclays were adjusted to three different release-kinetic models, demonstrating the Korsmeyer–Peppas model with release dependence on (i) the organic–inorganic hybrid system, and (ii) the nature of loaded molecules and their interaction with the support. Furthermore, in vitro cell viability assays were carried out with Caco-2 cells, demonstrating that the organonanoclays are well tolerated by cells at particle concentrations of ca. 50 μg/mL. MDPI 2022-08-05 /pmc/articles/PMC9370449/ /pubmed/35957126 http://dx.doi.org/10.3390/nano12152694 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
Poyatos-Racionero, Elisa
Pérez-Esteve, Édgar
Medaglia, Serena
Aznar, Elena
Barat, José M.
Martínez-Máñez, Ramón
Marcos, Maria Dolores
Bernardos, Andrea
Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus
title Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus
title_full Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus
title_fullStr Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus
title_full_unstemmed Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus
title_short Gated Organonanoclays for Large Biomolecules: Controlled Release Triggered by Surfactant Stimulus
title_sort gated organonanoclays for large biomolecules: controlled release triggered by surfactant stimulus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9370449/
https://www.ncbi.nlm.nih.gov/pubmed/35957126
http://dx.doi.org/10.3390/nano12152694
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