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Preparation and Characterization of Chitosan-Alginate Microspheres Loaded with Quercetin

The aim of this paper was to formulate microspheres based on biodegradable polymers (chitosan and sodium alginate), using the complex coacervation technique. Subsequently, the prepared microspheres were loaded with quercetin (QUE), a pharmacological active ingredient insoluble in water and unstable...

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Detalles Bibliográficos
Autores principales: Frenț, Olimpia Daniela, Duteanu, Narcis, Teusdea, Alin Cristian, Ciocan, Stefania, Vicaș, Laura, Jurca, Tunde, Muresan, Mariana, Pallag, Annamaria, Ianasi, Paula, Marian, Eleonora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839549/
https://www.ncbi.nlm.nih.gov/pubmed/35160478
http://dx.doi.org/10.3390/polym14030490
Descripción
Sumario:The aim of this paper was to formulate microspheres based on biodegradable polymers (chitosan and sodium alginate), using the complex coacervation technique. Subsequently, the prepared microspheres were loaded with quercetin (QUE), a pharmacological active ingredient insoluble in water and unstable to light, temperature and air. After preparation, the loaded microspheres underwent several studies for physical chemical characterization (performed by scanning electron microscopy—SEM, laser 3D scanning, and thermal analysis—TA). Furthermore, they were analyzed in order to obtain information regarding swelling index, drug entrapment, and in vitro release capacity. The obtained experimental data demonstrated 86.07% entrapment of QUE into the microspheres, in the case of the one with the highest Ch concentration. Additionally, it was proved that such systems allow the controlled release of the active drug over 24 h at the intestinal level. SEM micrographs proved that the prepared microspheres have a wrinkled surface, with compact structures and a large number of folds. On the basis of the TA analysis, it was concluded that the obtained microspheres were thermally stable, facilitating their usage at normal physiological temperatures as drug delivery systems.