Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication

ABSTRACT: Recently, one of the promising strategies to fight sensitive and resistant bacteria, and decrease the morbidity and mortality rates due to non-nosocomial infections, is to use antibiotic-loaded nanoparticles. In this study, ampicillin-loaded chitosan–polyanion nanoparticles were produced t...

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Autores:
Ciro Monsalve, Yhors Alexander
Rojas Camargo, John Jairo
Oñate Garzón, José Fernando
Salamanca Mejía, Constain Hugo
Tipo de recurso:
Article of investigation
Fecha de publicación:
2019
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/38230
Acceso en línea:
https://hdl.handle.net/10495/38230
Palabra clave:
Ampicilina
Ampicillin
Nanopartículas
Nanoparticles
Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Ultrasonido
Ultrasonics
Antiinfecciosos
Anti-Infective Agents
https://id.nlm.nih.gov/mesh/D000667
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D014465
https://id.nlm.nih.gov/mesh/D000890
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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repository_id_str
dc.title.spa.fl_str_mv Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
title Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
spellingShingle Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
Ampicilina
Ampicillin
Nanopartículas
Nanoparticles
Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Ultrasonido
Ultrasonics
Antiinfecciosos
Anti-Infective Agents
https://id.nlm.nih.gov/mesh/D000667
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D014465
https://id.nlm.nih.gov/mesh/D000890
title_short Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
title_full Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
title_fullStr Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
title_full_unstemmed Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
title_sort Synthesis, characterisation and biological evaluation of ampicillin-chitosan-polyanion nanoparticles produced by ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication
dc.creator.fl_str_mv Ciro Monsalve, Yhors Alexander
Rojas Camargo, John Jairo
Oñate Garzón, José Fernando
Salamanca Mejía, Constain Hugo
dc.contributor.author.none.fl_str_mv Ciro Monsalve, Yhors Alexander
Rojas Camargo, John Jairo
Oñate Garzón, José Fernando
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 Ampicilina
Ampicillin
Nanopartículas
Nanoparticles
Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Ultrasonido
Ultrasonics
Antiinfecciosos
Anti-Infective Agents
topic Ampicilina
Ampicillin
Nanopartículas
Nanoparticles
Quitosano
Chitosan
Polielectrolitos
Polyelectrolytes
Ultrasonido
Ultrasonics
Antiinfecciosos
Anti-Infective Agents
https://id.nlm.nih.gov/mesh/D000667
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D014465
https://id.nlm.nih.gov/mesh/D000890
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000667
https://id.nlm.nih.gov/mesh/D053758
https://id.nlm.nih.gov/mesh/D048271
https://id.nlm.nih.gov/mesh/D000071228
https://id.nlm.nih.gov/mesh/D014465
https://id.nlm.nih.gov/mesh/D000890
description ABSTRACT: Recently, one of the promising strategies to fight sensitive and resistant bacteria, and decrease the morbidity and mortality rates due to non-nosocomial infections, is to use antibiotic-loaded nanoparticles. In this study, ampicillin-loaded chitosan–polyanion nanoparticles were produced through the techniques of ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication, using several crosslinking agents, including phytic acid (non-polymeric polyanion), sodium and potassium salts of poly(maleic acid-alt-ethylene) and poly (maleic acid-alt-octadecene) (polymeric polyanions). These nanoparticles were analysed and characterised in terms of particle size, polydispersity index, zeta potential and encapsulation efficiency. The stability of these nanosystems was carried out at temperatures of 4 and 40 ◦C, and the antimicrobial effect was determined by the broth microdilution method using sensitive and resistant Staphylococcus aureus strains. The results reveal that most of the nanosystems have sizes <220 nm, positive zeta potential values and a monodisperse population, except for the nanoparticles crosslinked with PAM-18 polyanions. The nanometric systems exhibited adequate stability preventing aggregation and revealed a two-fold increase in antimicrobial activity when compared with free ampicillin. This study demonstrates the potential application of synthesised nanoparticles in the field of medicine, especially for treating infections caused by pathogenic S. aureus strains.
publishDate 2019
dc.date.issued.none.fl_str_mv 2019
dc.date.accessioned.none.fl_str_mv 2024-02-19T21:39:47Z
dc.date.available.none.fl_str_mv 2024-02-19T21:39:47Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/38230
dc.identifier.doi.none.fl_str_mv 10.3390/polym11111758
dc.identifier.eissn.none.fl_str_mv 2073-4360
url https://hdl.handle.net/10495/38230
identifier_str_mv 10.3390/polym11111758
2073-4360
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Polymers
dc.relation.citationendpage.spa.fl_str_mv 16
dc.relation.citationissue.spa.fl_str_mv 11
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dc.relation.citationvolume.spa.fl_str_mv 11
dc.relation.ispartofjournal.spa.fl_str_mv Polymers
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dc.format.extent.spa.fl_str_mv 16 páginas
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spelling Ciro Monsalve, Yhors AlexanderRojas Camargo, John JairoOñate Garzón, José FernandoSalamanca Mejía, Constain HugoDiseño y Formulación de Medicamentos Cosméticos y Afines2024-02-19T21:39:47Z2024-02-19T21:39:47Z2019https://hdl.handle.net/10495/3823010.3390/polym111117582073-4360ABSTRACT: Recently, one of the promising strategies to fight sensitive and resistant bacteria, and decrease the morbidity and mortality rates due to non-nosocomial infections, is to use antibiotic-loaded nanoparticles. In this study, ampicillin-loaded chitosan–polyanion nanoparticles were produced through the techniques of ionic gelation and polyelectrolyte complexation assisted by high-intensity sonication, using several crosslinking agents, including phytic acid (non-polymeric polyanion), sodium and potassium salts of poly(maleic acid-alt-ethylene) and poly (maleic acid-alt-octadecene) (polymeric polyanions). These nanoparticles were analysed and characterised in terms of particle size, polydispersity index, zeta potential and encapsulation efficiency. The stability of these nanosystems was carried out at temperatures of 4 and 40 ◦C, and the antimicrobial effect was determined by the broth microdilution method using sensitive and resistant Staphylococcus aureus strains. The results reveal that most of the nanosystems have sizes <220 nm, positive zeta potential values and a monodisperse population, except for the nanoparticles crosslinked with PAM-18 polyanions. The nanometric systems exhibited adequate stability preventing aggregation and revealed a two-fold increase in antimicrobial activity when compared with free ampicillin. This study demonstrates the potential application of synthesised nanoparticles in the field of medicine, especially for treating infections caused by pathogenic S. aureus strains.Colombia. 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