Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes

Detalhes bibliográficos
Autor(a) principal: Agostini, Sandra Barbosa Neder
Data de Publicação: 2023
Outros Autores: Machado, Victor Lima de Sousa, Virtuoso, Luciano Sindra, Nogueira, Denismar Alves, Pereira, Gislaine Ribeiro, Carvalho, Flavia Chiva
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
DOI: 10.1590/s2175-97902022e20621
Texto Completo: https://www.revistas.usp.br/bjps/article/view/208732
Resumo: Polyelectrolyte complexes (PECs) as drug delivery systems are widely explored since they are easily obtained by coacervation and biopolymers can be associated. However, particle distribution is a challenging critical parameter that has been infrequently focused. This work evaluated the effect of NaCl concentration on the physicochemical properties of PECs based on chitosan and hypromellose loaded with methotrexate. The particle size, zeta potential and polydispersity index (PdI) were determined by DLS, besides of drug entrapment efficiency (EE) and in vitro drug release profile determination. Particle size decreased while NaCl concentration rised, achieving a narrower size distribution of (345±79 nm) and PdI (0.285±0.067) with 200 mmol/L NaCl. The higher the NaCl concentration, the lower the zeta potential at acid pH. The EE was kept similar ((28.2±4.5) %) from 0 to 300 mmol/L NaCl, while 400 mmol/L NaCl impaired the drug entrapment. The addition of (200 and 300) mmol/L NaCl did not affect the drug release profile, but it was faster with (100 or 400) mmol/L. In conclusion, the addition of 200 mmol/L NaCl reduced particle size and PdI with no changes in the EE and drug release. Therefore, the ionic strength plays an important role on PECs development.
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spelling Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexesPolyelectrolyte complexChitosanIonic strengthPolydispersityNanoparticlesPolyelectrolyte complexes (PECs) as drug delivery systems are widely explored since they are easily obtained by coacervation and biopolymers can be associated. However, particle distribution is a challenging critical parameter that has been infrequently focused. This work evaluated the effect of NaCl concentration on the physicochemical properties of PECs based on chitosan and hypromellose loaded with methotrexate. The particle size, zeta potential and polydispersity index (PdI) were determined by DLS, besides of drug entrapment efficiency (EE) and in vitro drug release profile determination. Particle size decreased while NaCl concentration rised, achieving a narrower size distribution of (345±79 nm) and PdI (0.285±0.067) with 200 mmol/L NaCl. The higher the NaCl concentration, the lower the zeta potential at acid pH. The EE was kept similar ((28.2±4.5) %) from 0 to 300 mmol/L NaCl, while 400 mmol/L NaCl impaired the drug entrapment. The addition of (200 and 300) mmol/L NaCl did not affect the drug release profile, but it was faster with (100 or 400) mmol/L. In conclusion, the addition of 200 mmol/L NaCl reduced particle size and PdI with no changes in the EE and drug release. Therefore, the ionic strength plays an important role on PECs development.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-02-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/20873210.1590/s2175-97902022e20621Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/208732/197468Copyright (c) 2022 Brazilian Journal of Pharmaceutical Scienceshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAgostini, Sandra Barbosa NederMachado, Victor Lima de SousaVirtuoso, Luciano SindraNogueira, Denismar AlvesPereira, Gislaine RibeiroCarvalho, Flavia Chiva2023-08-23T18:24:51Zoai:revistas.usp.br:article/208732Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-08-23T18:24:51Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
title Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
spellingShingle Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
Agostini, Sandra Barbosa Neder
Polyelectrolyte complex
Chitosan
Ionic strength
Polydispersity
Nanoparticles
Agostini, Sandra Barbosa Neder
Polyelectrolyte complex
Chitosan
Ionic strength
Polydispersity
Nanoparticles
title_short Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
title_full Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
title_fullStr Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
title_full_unstemmed Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
title_sort Influence of the ionic strength on the physicochemical properties of methotrexate-loaded chitosan polyelectrolyte complexes
author Agostini, Sandra Barbosa Neder
author_facet Agostini, Sandra Barbosa Neder
Agostini, Sandra Barbosa Neder
Machado, Victor Lima de Sousa
Virtuoso, Luciano Sindra
Nogueira, Denismar Alves
Pereira, Gislaine Ribeiro
Carvalho, Flavia Chiva
Machado, Victor Lima de Sousa
Virtuoso, Luciano Sindra
Nogueira, Denismar Alves
Pereira, Gislaine Ribeiro
Carvalho, Flavia Chiva
author_role author
author2 Machado, Victor Lima de Sousa
Virtuoso, Luciano Sindra
Nogueira, Denismar Alves
Pereira, Gislaine Ribeiro
Carvalho, Flavia Chiva
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Agostini, Sandra Barbosa Neder
Machado, Victor Lima de Sousa
Virtuoso, Luciano Sindra
Nogueira, Denismar Alves
Pereira, Gislaine Ribeiro
Carvalho, Flavia Chiva
dc.subject.por.fl_str_mv Polyelectrolyte complex
Chitosan
Ionic strength
Polydispersity
Nanoparticles
topic Polyelectrolyte complex
Chitosan
Ionic strength
Polydispersity
Nanoparticles
description Polyelectrolyte complexes (PECs) as drug delivery systems are widely explored since they are easily obtained by coacervation and biopolymers can be associated. However, particle distribution is a challenging critical parameter that has been infrequently focused. This work evaluated the effect of NaCl concentration on the physicochemical properties of PECs based on chitosan and hypromellose loaded with methotrexate. The particle size, zeta potential and polydispersity index (PdI) were determined by DLS, besides of drug entrapment efficiency (EE) and in vitro drug release profile determination. Particle size decreased while NaCl concentration rised, achieving a narrower size distribution of (345±79 nm) and PdI (0.285±0.067) with 200 mmol/L NaCl. The higher the NaCl concentration, the lower the zeta potential at acid pH. The EE was kept similar ((28.2±4.5) %) from 0 to 300 mmol/L NaCl, while 400 mmol/L NaCl impaired the drug entrapment. The addition of (200 and 300) mmol/L NaCl did not affect the drug release profile, but it was faster with (100 or 400) mmol/L. In conclusion, the addition of 200 mmol/L NaCl reduced particle size and PdI with no changes in the EE and drug release. Therefore, the ionic strength plays an important role on PECs development.
publishDate 2023
dc.date.none.fl_str_mv 2023-02-28
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://www.revistas.usp.br/bjps/article/view/208732
10.1590/s2175-97902022e20621
url https://www.revistas.usp.br/bjps/article/view/208732
identifier_str_mv 10.1590/s2175-97902022e20621
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/208732/197468
dc.rights.driver.fl_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)
Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)
Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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dc.identifier.doi.none.fl_str_mv 10.1590/s2175-97902022e20621