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

Detalhes bibliográficos
Autor(a) principal: Gomes, Felipe Pereira
Data de Publicação: 2022
Outros Autores: Cruz, Letícia, Ferreira, Luana Mota
Tipo de documento: Artigo
Idioma: por
Título da fonte: Saúde (Santa Maria)
Texto Completo: https://periodicos.ufsm.br/revistasaude/article/view/66366
Resumo: 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.
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spelling Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis managementSodium risedronate-loaded poly(ε-caprolactone) nanoparticles: Development, physicochemical characterization, and in vitro drug release studyosteoporosissodium risedronatenanostructured systemssolvent emulsification/evaporation method.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.Population in all over the world is affected by bone diseases, such as osteoporosis and loss bone tissue. 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 and characterize Na-Ris-loaded nanoparticles, as well as 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, a nanocarrier containing a water-soluble drug was successfully developed, presenting adequate physicochemical characteristics, which can be promising for biological evaluations.Universidade Federal de Santa Maria2022-07-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://periodicos.ufsm.br/revistasaude/article/view/66366Saúde (Santa Maria); Revista Saúde (Santa Maria). 2022, v. 48, n. 1Saúde (Santa Maria); Revista Saúde (Santa Maria). 2022, v. 48, n. 12236-58340103-4499reponame:Saúde (Santa Maria)instname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMporhttps://periodicos.ufsm.br/revistasaude/article/view/66366/47872Copyright (c) 2022 Saúde (Santa Maria)info:eu-repo/semantics/openAccessGomes, Felipe PereiraCruz, LetíciaFerreira, Luana Mota2022-07-15T08:42:06Zoai:ojs.pkp.sfu.ca:article/66366Revistahttps://periodicos.ufsm.br/revistasaudePUBhttps://periodicos.ufsm.br/revistasaude/oairevistasaude.ufsm@gmail.com || amanda.revsaude@gmail.com || beatriz.revsaude@gmail.com2236-58342236-5834opendoar:2022-07-15T08:42:06Saúde (Santa Maria) - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
Sodium risedronate-loaded poly(ε-caprolactone) nanoparticles: Development, physicochemical characterization, and in vitro drug release study
title Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
spellingShingle Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
Gomes, Felipe Pereira
osteoporosis
sodium risedronate
nanostructured systems
solvent emulsification/evaporation method.
title_short Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
title_full Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
title_fullStr Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
title_full_unstemmed Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
title_sort Design of sodium risedronate-loaded poly(ɛ-caprolactone) nanoparticles: a promising approach for osteoporosis management
author Gomes, Felipe Pereira
author_facet Gomes, Felipe Pereira
Cruz, Letícia
Ferreira, Luana Mota
author_role author
author2 Cruz, Letícia
Ferreira, Luana Mota
author2_role author
author
dc.contributor.author.fl_str_mv Gomes, Felipe Pereira
Cruz, Letícia
Ferreira, Luana Mota
dc.subject.por.fl_str_mv osteoporosis
sodium risedronate
nanostructured systems
solvent emulsification/evaporation method.
topic osteoporosis
sodium risedronate
nanostructured systems
solvent emulsification/evaporation method.
description 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.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-15
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://periodicos.ufsm.br/revistasaude/article/view/66366
url https://periodicos.ufsm.br/revistasaude/article/view/66366
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://periodicos.ufsm.br/revistasaude/article/view/66366/47872
dc.rights.driver.fl_str_mv Copyright (c) 2022 Saúde (Santa Maria)
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Saúde (Santa Maria)
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
publisher.none.fl_str_mv Universidade Federal de Santa Maria
dc.source.none.fl_str_mv Saúde (Santa Maria); Revista Saúde (Santa Maria). 2022, v. 48, n. 1
Saúde (Santa Maria); Revista Saúde (Santa Maria). 2022, v. 48, n. 1
2236-5834
0103-4499
reponame:Saúde (Santa Maria)
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Saúde (Santa Maria)
collection Saúde (Santa Maria)
repository.name.fl_str_mv Saúde (Santa Maria) - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv revistasaude.ufsm@gmail.com || amanda.revsaude@gmail.com || beatriz.revsaude@gmail.com
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