Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate

ABSTRACT: A promising strategy to improve the effectivity of anticancer treatment and decrease its side effects is to modulate drug release by using nanoparticulates (NPs) as carriers. In this study, methotrexate-loaded chitosan–polyanion nanoparticles were produced by polyelectrolyte complexation a...

Full description

Autores:
Ciro Monsalve, Yhors Alexander
Rojas Camargo, John Jairo
Carabali Balanta, Gustavo Adolfo
Alhajj Agualimpia, María José
Salamanca Mejía, Constain Hugo
Tipo de recurso:
Article of investigation
Fecha de publicación:
2020
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/38229
Acceso en línea:
https://hdl.handle.net/10495/38229
Palabra clave:
Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Nanopartículas
Nanoparticles
Metotrexato
Methotrexate
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D008727
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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dc.title.spa.fl_str_mv Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
title Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
spellingShingle Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Nanopartículas
Nanoparticles
Metotrexato
Methotrexate
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D008727
title_short Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
title_full Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
title_fullStr Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
title_full_unstemmed Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
title_sort Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexate
dc.creator.fl_str_mv Ciro Monsalve, Yhors Alexander
Rojas Camargo, John Jairo
Carabali Balanta, Gustavo Adolfo
Alhajj Agualimpia, María José
Salamanca Mejía, Constain Hugo
dc.contributor.author.none.fl_str_mv Ciro Monsalve, Yhors Alexander
Rojas Camargo, John Jairo
Carabali Balanta, Gustavo Adolfo
Alhajj Agualimpia, María José
Salamanca Mejía, Constain Hugo
dc.contributor.researchgroup.spa.fl_str_mv Diseño y Formulación de Medicamentos Cosméticos y Afines
dc.subject.decs.none.fl_str_mv Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Nanopartículas
Nanoparticles
Metotrexato
Methotrexate
topic Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Nanopartículas
Nanoparticles
Metotrexato
Methotrexate
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D008727
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D008727
description ABSTRACT: A promising strategy to improve the effectivity of anticancer treatment and decrease its side effects is to modulate drug release by using nanoparticulates (NPs) as carriers. In this study, methotrexate-loaded chitosan–polyanion nanoparticles were produced by polyelectrolyte complexation assisted by high-intensity sonication, using several anionic polymers, such as the sodium and potassium salts of poly(maleic acid-alt-ethylene) and poly (maleic acid-alt-octadecene), here named PAM-2 and PAM-18, respectively. Such NPs were analyzed and characterized according to particle size, polydispersity index, zeta potential and encapsulation efficiency. Likewise, their physical stability was tested at 4 ◦C and 40 ◦C in order to evaluate any change in the previously mentioned particle parameters. The in vitro methotrexate release was assessed at a pH of 7.4, which simulated physiological conditions, and the data were fitted to the heuristic models of order one, Higuchi, Peppas–Sahlin and Korsmeyer–Peppas. The results revealed that most of the MTX-chitosan–polyanion NPs have positive zeta potential values, sizes <280 nm and monodisperse populations, except for the NPs formed with PAM-18 polyanions. Further, the NPs showed adequate physical stability, preventing NP–NP aggregation. Likewise, these carriers modified the MTX release by an anomalous mechanism, where the NPs formed with PAM-2 polymer led to a release mechanism controlled by diffusion and relaxation, whereas the NPs formed with PAM-18 led to a mainly diffusion-controlled release mechanism.
publishDate 2020
dc.date.issued.none.fl_str_mv 2020
dc.date.accessioned.none.fl_str_mv 2024-02-19T21:28:14Z
dc.date.available.none.fl_str_mv 2024-02-19T21:28:14Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.issn.none.fl_str_mv 1424-8247
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/38229
dc.identifier.doi.none.fl_str_mv 10.3390/ph13010011
identifier_str_mv 1424-8247
10.3390/ph13010011
url https://hdl.handle.net/10495/38229
dc.language.iso.spa.fl_str_mv eng
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dc.relation.ispartofjournalabbrev.spa.fl_str_mv Pharmaceuticals
dc.relation.citationendpage.spa.fl_str_mv 14
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dc.relation.citationvolume.spa.fl_str_mv 13
dc.relation.ispartofjournal.spa.fl_str_mv Pharmaceuticals
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dc.format.extent.spa.fl_str_mv 14 páginas
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dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
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spelling Ciro Monsalve, Yhors AlexanderRojas Camargo, John JairoCarabali Balanta, Gustavo AdolfoAlhajj Agualimpia, María JoséSalamanca Mejía, Constain HugoDiseño y Formulación de Medicamentos Cosméticos y Afines2024-02-19T21:28:14Z2024-02-19T21:28:14Z20201424-8247https://hdl.handle.net/10495/3822910.3390/ph13010011ABSTRACT: A promising strategy to improve the effectivity of anticancer treatment and decrease its side effects is to modulate drug release by using nanoparticulates (NPs) as carriers. In this study, methotrexate-loaded chitosan–polyanion nanoparticles were produced by polyelectrolyte complexation assisted by high-intensity sonication, using several anionic polymers, such as the sodium and potassium salts of poly(maleic acid-alt-ethylene) and poly (maleic acid-alt-octadecene), here named PAM-2 and PAM-18, respectively. Such NPs were analyzed and characterized according to particle size, polydispersity index, zeta potential and encapsulation efficiency. Likewise, their physical stability was tested at 4 ◦C and 40 ◦C in order to evaluate any change in the previously mentioned particle parameters. The in vitro methotrexate release was assessed at a pH of 7.4, which simulated physiological conditions, and the data were fitted to the heuristic models of order one, Higuchi, Peppas–Sahlin and Korsmeyer–Peppas. The results revealed that most of the MTX-chitosan–polyanion NPs have positive zeta potential values, sizes <280 nm and monodisperse populations, except for the NPs formed with PAM-18 polyanions. Further, the NPs showed adequate physical stability, preventing NP–NP aggregation. Likewise, these carriers modified the MTX release by an anomalous mechanism, where the NPs formed with PAM-2 polymer led to a release mechanism controlled by diffusion and relaxation, whereas the NPs formed with PAM-18 led to a mainly diffusion-controlled release mechanism.Colombia. 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