Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management

Objective: Osteoporosis is a chronic disease characterized by bone mass loss. Sodium risedronate (Na-Ris) is one of the most used drugs to its treatment. However, it has low oral bioavailability and exhibits many side effects. In order to overcome these limitations, the search for new dosage forms i...

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Detalles Bibliográficos
Autores: Gomes, Felipe Pereira, Cruz, Letícia, Ferreira, Luana Mota
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:Brasil
Institución:Universidade Federal de Santa Maria (UFSM)
Repositorio:Saúde (Santa Maria)
Idioma:portugués
OAI Identifier:oai:ojs.pkp.sfu.ca:article/66366
Acceso en línea:https://periodicos.ufsm.br/revistasaude/article/view/66366
Access Level:acceso abierto
Palabra clave:osteoporosis
sodium risedronate
nanostructured systems
solvent emulsification/evaporation method.
Descripción
Sumario:Objective: Osteoporosis is a chronic disease characterized by bone mass loss. Sodium risedronate (Na-Ris) is one of the most used drugs to its treatment. However, it has low oral bioavailability and exhibits many side effects. In order to overcome these limitations, the search for new dosage forms is necessary. One of these alternatives is the development of nanoparticles, which are able to transport the drug to its target directly, promoting maximization of the therapeutic efficiency and minimization of the toxicity. Due to its great versatility, these systems can be applied to an assorted administration routes, such as oral, pulmonary, intravenous, among others. Thus, the objective of this study was to develop Na-Ris-loaded nanoparticles and determine the drug release profile. Methods: Nanoparticles were prepared by solvent emulsification/evaporation method and characterized by mean size, polydispersity index, zeta potential, granulometric distribution, drug content and encapsulation efficiency. Afterwards, in vitro drug release was performed using the dialysis bag technique as well as the release kinetics were also studied. Results: The developed system has shown mean size of 193 ± 14 nm and polydispersity index around 0.2. Zeta potential was -9.76 ± 0,52 mV and slightly acid values for pH. The granulometric distribution demonstrated nanoparticles with a narrow size distribution and the absence of particles in the micrometer range. Regarding the in vitro release, the drug was released completely from the system in 240 minutes and the release kinetics has follow the zero-order equation. Final considerations: Thus, the Na-Ris-loaded nanoparticles were successfully developed and are a promising formulation for osteoporosis management.