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Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation

This study was aimed at preparing and characterizing solid lipid nanoparticles loading rutin (RT-SLNs) for the treatment of oxidative stress-induced diseases. Phospholipon 80H(®) as a solid lipid and Polysorbate 80 as surfactant were used for the SLNs preparation, using the solvent emulsification/di...

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Autores principales: De Gaetano, Federica, Cristiano, Maria Chiara, Venuti, Valentina, Crupi, Vincenza, Majolino, Domenico, Paladini, Giuseppe, Acri, Giuseppe, Testagrossa, Barbara, Irrera, Alessia, Paolino, Donatella, Tommasini, Silvana, Ventura, Cinzia Anna, Stancanelli, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920302/
https://www.ncbi.nlm.nih.gov/pubmed/33669321
http://dx.doi.org/10.3390/molecules26041039
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author De Gaetano, Federica
Cristiano, Maria Chiara
Venuti, Valentina
Crupi, Vincenza
Majolino, Domenico
Paladini, Giuseppe
Acri, Giuseppe
Testagrossa, Barbara
Irrera, Alessia
Paolino, Donatella
Tommasini, Silvana
Ventura, Cinzia Anna
Stancanelli, Rosanna
author_facet De Gaetano, Federica
Cristiano, Maria Chiara
Venuti, Valentina
Crupi, Vincenza
Majolino, Domenico
Paladini, Giuseppe
Acri, Giuseppe
Testagrossa, Barbara
Irrera, Alessia
Paolino, Donatella
Tommasini, Silvana
Ventura, Cinzia Anna
Stancanelli, Rosanna
author_sort De Gaetano, Federica
collection PubMed
description This study was aimed at preparing and characterizing solid lipid nanoparticles loading rutin (RT-SLNs) for the treatment of oxidative stress-induced diseases. Phospholipon 80H(®) as a solid lipid and Polysorbate 80 as surfactant were used for the SLNs preparation, using the solvent emulsification/diffusion method. We obtained spherical RT-SLNs with low sizes, ranging from 40 to 60 nm (hydrodynamic radius) for the SLNs prepared starting from 2% and 5% (w/w) theoretical amount. All prepared formulations showed negative zeta-potential values. RT was efficiently encapsulated within SLNs, obtaining high encapsulation efficiency and drug content percentages, particularly for SLNs prepared with a 5% theoretical amount of RT. In vitro release profiles and analysis of the obtained data applying different kinetic models revealed Fickian diffusion as the main mechanism of RT release from the SLNs. The morphology of RT-SLNs was characterized by scanning electron microscopy (SEM), whereas the interactions between RT and the lipid matrix were investigated by Raman spectroscopy, evidencing spectral modifications of characteristic bands of RT due to the establishment of new interactions. Finally, antioxidant activity assay on human glioblastoma astrocytoma (U373) culture cells showed a dose-dependent activity for RT-SLNs, particularly at the highest assayed dose (50 μM), whereas the free drug showed the lesser activity.
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spelling pubmed-79203022021-03-02 Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation De Gaetano, Federica Cristiano, Maria Chiara Venuti, Valentina Crupi, Vincenza Majolino, Domenico Paladini, Giuseppe Acri, Giuseppe Testagrossa, Barbara Irrera, Alessia Paolino, Donatella Tommasini, Silvana Ventura, Cinzia Anna Stancanelli, Rosanna Molecules Article This study was aimed at preparing and characterizing solid lipid nanoparticles loading rutin (RT-SLNs) for the treatment of oxidative stress-induced diseases. Phospholipon 80H(®) as a solid lipid and Polysorbate 80 as surfactant were used for the SLNs preparation, using the solvent emulsification/diffusion method. We obtained spherical RT-SLNs with low sizes, ranging from 40 to 60 nm (hydrodynamic radius) for the SLNs prepared starting from 2% and 5% (w/w) theoretical amount. All prepared formulations showed negative zeta-potential values. RT was efficiently encapsulated within SLNs, obtaining high encapsulation efficiency and drug content percentages, particularly for SLNs prepared with a 5% theoretical amount of RT. In vitro release profiles and analysis of the obtained data applying different kinetic models revealed Fickian diffusion as the main mechanism of RT release from the SLNs. The morphology of RT-SLNs was characterized by scanning electron microscopy (SEM), whereas the interactions between RT and the lipid matrix were investigated by Raman spectroscopy, evidencing spectral modifications of characteristic bands of RT due to the establishment of new interactions. Finally, antioxidant activity assay on human glioblastoma astrocytoma (U373) culture cells showed a dose-dependent activity for RT-SLNs, particularly at the highest assayed dose (50 μM), whereas the free drug showed the lesser activity. MDPI 2021-02-16 /pmc/articles/PMC7920302/ /pubmed/33669321 http://dx.doi.org/10.3390/molecules26041039 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
De Gaetano, Federica
Cristiano, Maria Chiara
Venuti, Valentina
Crupi, Vincenza
Majolino, Domenico
Paladini, Giuseppe
Acri, Giuseppe
Testagrossa, Barbara
Irrera, Alessia
Paolino, Donatella
Tommasini, Silvana
Ventura, Cinzia Anna
Stancanelli, Rosanna
Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation
title Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation
title_full Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation
title_fullStr Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation
title_full_unstemmed Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation
title_short Rutin-Loaded Solid Lipid Nanoparticles: Characterization and In Vitro Evaluation
title_sort rutin-loaded solid lipid nanoparticles: characterization and in vitro evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920302/
https://www.ncbi.nlm.nih.gov/pubmed/33669321
http://dx.doi.org/10.3390/molecules26041039
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