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...
- 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 |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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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 |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Pharmaceuticals |
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14 |
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1 |
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1 |
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13 |
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Pharmaceuticals |
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https://creativecommons.org/licenses/by/4.0/ |
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http://creativecommons.org/licenses/by/2.5/co/ |
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info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/2.5/co/ http://purl.org/coar/access_right/c_abf2 |
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openAccess |
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14 páginas |
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application/pdf |
| dc.publisher.spa.fl_str_mv |
MDPI |
| dc.publisher.place.spa.fl_str_mv |
Basilea, Suiza |
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Universidad de Antioquia |
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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. Ministerio de Ciencia, Tecnología e InnovaciónCOL000362314 páginasapplication/pdfengMDPIBasilea, Suizahttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Production and characterization of chitosan-polyanion nanoparticles by polyelectrolyte complexation assisted by high-intensity sonication for the modified release of methotrexateArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionQuitosanoChitosanPolielectrolitosPolyelectrolytesNanopartículasNanoparticlesMetotrexatoMethotrexatehttps://id.nlm.nih.gov/mesh/D048271https://id.nlm.nih.gov/mesh/D000071228https://id.nlm.nih.gov/mesh/D053758https://id.nlm.nih.gov/mesh/D008727Pharmaceuticals141113Pharmaceuticals727-2015RoR:03fd5ne08PublicationCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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