DESARROLLO DE NANOPARTÍCULAS DE QUITOSANO-GELATINA Y QUITOSANO-COLÁGENO PARA LIBERACIÓN DE FÁRMACOS
Polymeric nanoparticles have demonstrated a great potential for biomedical application, especially in drug delivery systems acting as nanocarriers. The polymers obtained from living organisms, known as biopolymers, are promising materials for these purposes since they present biodegradability, bioco...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2023 |
| País: | Perú |
| Institución: | Sociedad Química del Perú |
| Repositorio: | Revista de la Sociedad Química del Perú |
| Idioma: | español |
| OAI Identifier: | oai:rsqp.revistas.sqperu.org.pe:article/428 |
| Acceso en línea: | https://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/428 |
| Access Level: | acceso abierto |
| Palabra clave: | chitosan collagen gelatin nanoparticles drug release quitosano colágeno gelatina nanopartículas liberación de fármacos |
| Sumario: | Polymeric nanoparticles have demonstrated a great potential for biomedical application, especially in drug delivery systems acting as nanocarriers. The polymers obtained from living organisms, known as biopolymers, are promising materials for these purposes since they present biodegradability, biocompatibility and low immunogenicity, which are features required for in vivo applications. In this work, polymeric nanoparticles were prepared from mixtures of biopolymers such as chitosan, collagen and gelatin by ionic reticulation with sodium tripolyphosphate. Picric acid as a model drug was encapsulated into the nanoparticles. Chitosan of 50.4 kDa of molecular weight and 81 % of deacetylation degree was prepared through the deacetylation and depolymerization of chitin extracted from squid pens (Loligo sp). The composition, size distribution, and surface charge of the prepared nanoparticles were evaluated. Moreover, the influence of the nanoparticles mass and picric acid concentration were analyzed during the loading process by determining of the loaded content and the incorporation efficiency. Maximum loaded contents of picric acid were 7.16 % and 6.45 % for chitosan/gelatin nanoparticles and chitosan/collagen nanoparticles, respectively. In vitro release tests showed a quick picric acid release in chitosan/gelatin nanoparticles. The nanoparticles prepared with collagen took longer time to release the picric acid. Kinetic studies, using mathematical models, revealed that the release takes place through a diffusion mechanism. |
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