Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs
- Autores
- Des Bouillons Gamboa, Rosvin E.; Montes de Oca, Gabriela; Baudrit, Jose Roberto Vega; Ríos Duarte, Liz Carolina; Lopretti, Mary; Rentería Urquiza, Maite; Zúñiga Umaña, Juan Miguel; Barreiro, Filomena; Vazquez, Patricia Graciela
- Año de publicación
- 2024
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- In the face of a pressing global issue-the escalating threat of antibiotic resistance-the development of new antimicrobial agents is urgent. Nanotechnology, with its innovative approach, emerges as a promising solution to enhance the efficacy of these agents and combat the challenge of microbial resistance. Chitosan nanoparticles (CSNPs) stand out in biomedical applications, particularly in the controlled release of antibiotics, with their unique properties such as biocompatibility, stability, biodegradability, non-toxicity, and simple synthesis processes suitable for sensitive molecules. This study synthesized CSNPs using the ionotropic gelation method, with tripolyphosphate (TPP) as the crosslinking agent. Various CS: TPP ratios (6:1, 5:1, 4:1, 3:1, 2:1) were tested, and the resulting nanoparticles were evaluated using dynamic light scattering (DLS). The CS: TPP ratio of 4:1, with an average hydrodynamic diameter (DHP) of (195 ± 10) nm and a zeta potential of (51 ± 1) mV, was identified as the most suitable for further analysis. The characterization of NPs by Transmission Electron Microscope (TEM) and atomic force microscopy (AFM) revealed diameters of (65 ± 14) nm and (102 ± 18) nm, respectively. Notably, CSNPs exhibited significant aggregation during centrifugation and lyophilization, leading to diameter increases of up to 285% as measured by AFM. The antibacterial activity of CSNPs against Staphylococcus aureus and Escherichia coli was assessed using the resazurin assay. It was found that CSNPs not subjected to centrifugation, freezing, and lyophilization retained their antimicrobial activity. In contrast, those that underwent these processes lost their efficacy, likely due to aggregation and destabilization of the system. This study presents a straightforward and effective protocol for encapsulating sensitive active agents and synthesizing chitosan nanoparticles, a potential system with significant implications in the fight against antibiotic resistance.
Fil: Des Bouillons Gamboa, Rosvin E.. Laboratorio Nacional de Nanotecnología; Costa Rica. Tecnológico de Costa Rica; Costa Rica
Fil: Montes de Oca, Gabriela. Laboratorio Nacional de Nanotecnología; Costa Rica
Fil: Baudrit, Jose Roberto Vega. Laboratorio Nacional de Nanotecnología; Costa Rica
Fil: Ríos Duarte, Liz Carolina. Universidad Autonoma de Asuncion.; Paraguay
Fil: Lopretti, Mary. Universidad de la República; Uruguay
Fil: Rentería Urquiza, Maite. Universidad de Guadalajara; México
Fil: Zúñiga Umaña, Juan Miguel. Universidad de Guadalajara; México
Fil: Barreiro, Filomena. Instituto Politécnico de Bragança.; Portugal
Fil: Vazquez, Patricia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Ciencias Aplicadas "Dr. Jorge J. Ronco". Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Ciencias Aplicadas; Argentina - Materia
-
chitosan
antibiotic resistance,
nanoparticles
AFM, DLS, TEM - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/264981
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oai:ri.conicet.gov.ar:11336/264981 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
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Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPsDes Bouillons Gamboa, Rosvin E.Montes de Oca, GabrielaBaudrit, Jose Roberto VegaRíos Duarte, Liz CarolinaLopretti, MaryRentería Urquiza, MaiteZúñiga Umaña, Juan MiguelBarreiro, FilomenaVazquez, Patricia Gracielachitosanantibiotic resistance,nanoparticlesAFM, DLS, TEMhttps://purl.org/becyt/ford/2.10https://purl.org/becyt/ford/2In the face of a pressing global issue-the escalating threat of antibiotic resistance-the development of new antimicrobial agents is urgent. Nanotechnology, with its innovative approach, emerges as a promising solution to enhance the efficacy of these agents and combat the challenge of microbial resistance. Chitosan nanoparticles (CSNPs) stand out in biomedical applications, particularly in the controlled release of antibiotics, with their unique properties such as biocompatibility, stability, biodegradability, non-toxicity, and simple synthesis processes suitable for sensitive molecules. This study synthesized CSNPs using the ionotropic gelation method, with tripolyphosphate (TPP) as the crosslinking agent. Various CS: TPP ratios (6:1, 5:1, 4:1, 3:1, 2:1) were tested, and the resulting nanoparticles were evaluated using dynamic light scattering (DLS). The CS: TPP ratio of 4:1, with an average hydrodynamic diameter (DHP) of (195 ± 10) nm and a zeta potential of (51 ± 1) mV, was identified as the most suitable for further analysis. The characterization of NPs by Transmission Electron Microscope (TEM) and atomic force microscopy (AFM) revealed diameters of (65 ± 14) nm and (102 ± 18) nm, respectively. Notably, CSNPs exhibited significant aggregation during centrifugation and lyophilization, leading to diameter increases of up to 285% as measured by AFM. The antibacterial activity of CSNPs against Staphylococcus aureus and Escherichia coli was assessed using the resazurin assay. It was found that CSNPs not subjected to centrifugation, freezing, and lyophilization retained their antimicrobial activity. In contrast, those that underwent these processes lost their efficacy, likely due to aggregation and destabilization of the system. This study presents a straightforward and effective protocol for encapsulating sensitive active agents and synthesizing chitosan nanoparticles, a potential system with significant implications in the fight against antibiotic resistance.Fil: Des Bouillons Gamboa, Rosvin E.. Laboratorio Nacional de Nanotecnología; Costa Rica. Tecnológico de Costa Rica; Costa RicaFil: Montes de Oca, Gabriela. Laboratorio Nacional de Nanotecnología; Costa RicaFil: Baudrit, Jose Roberto Vega. Laboratorio Nacional de Nanotecnología; Costa RicaFil: Ríos Duarte, Liz Carolina. Universidad Autonoma de Asuncion.; ParaguayFil: Lopretti, Mary. Universidad de la República; UruguayFil: Rentería Urquiza, Maite. Universidad de Guadalajara; MéxicoFil: Zúñiga Umaña, Juan Miguel. Universidad de Guadalajara; MéxicoFil: Barreiro, Filomena. Instituto Politécnico de Bragança.; PortugalFil: Vazquez, Patricia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Ciencias Aplicadas "Dr. Jorge J. Ronco". Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Ciencias Aplicadas; ArgentinaFrontiers Media2024-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/264981Des Bouillons Gamboa, Rosvin E.; Montes de Oca, Gabriela; Baudrit, Jose Roberto Vega; Ríos Duarte, Liz Carolina; Lopretti, Mary; et al.; Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs; Frontiers Media; Frontiers in Chemistry; 12; 11-2024; 1-142296-2646CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.frontiersin.org/articles/10.3389/fchem.2024.1469271/fullinfo:eu-repo/semantics/altIdentifier/doi/10.3389/fchem.2024.1469271info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:10:52Zoai:ri.conicet.gov.ar:11336/264981instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:10:53.086CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
title |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
spellingShingle |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs Des Bouillons Gamboa, Rosvin E. chitosan antibiotic resistance, nanoparticles AFM, DLS, TEM |
title_short |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
title_full |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
title_fullStr |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
title_full_unstemmed |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
title_sort |
Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs |
dc.creator.none.fl_str_mv |
Des Bouillons Gamboa, Rosvin E. Montes de Oca, Gabriela Baudrit, Jose Roberto Vega Ríos Duarte, Liz Carolina Lopretti, Mary Rentería Urquiza, Maite Zúñiga Umaña, Juan Miguel Barreiro, Filomena Vazquez, Patricia Graciela |
author |
Des Bouillons Gamboa, Rosvin E. |
author_facet |
Des Bouillons Gamboa, Rosvin E. Montes de Oca, Gabriela Baudrit, Jose Roberto Vega Ríos Duarte, Liz Carolina Lopretti, Mary Rentería Urquiza, Maite Zúñiga Umaña, Juan Miguel Barreiro, Filomena Vazquez, Patricia Graciela |
author_role |
author |
author2 |
Montes de Oca, Gabriela Baudrit, Jose Roberto Vega Ríos Duarte, Liz Carolina Lopretti, Mary Rentería Urquiza, Maite Zúñiga Umaña, Juan Miguel Barreiro, Filomena Vazquez, Patricia Graciela |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
chitosan antibiotic resistance, nanoparticles AFM, DLS, TEM |
topic |
chitosan antibiotic resistance, nanoparticles AFM, DLS, TEM |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.10 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
In the face of a pressing global issue-the escalating threat of antibiotic resistance-the development of new antimicrobial agents is urgent. Nanotechnology, with its innovative approach, emerges as a promising solution to enhance the efficacy of these agents and combat the challenge of microbial resistance. Chitosan nanoparticles (CSNPs) stand out in biomedical applications, particularly in the controlled release of antibiotics, with their unique properties such as biocompatibility, stability, biodegradability, non-toxicity, and simple synthesis processes suitable for sensitive molecules. This study synthesized CSNPs using the ionotropic gelation method, with tripolyphosphate (TPP) as the crosslinking agent. Various CS: TPP ratios (6:1, 5:1, 4:1, 3:1, 2:1) were tested, and the resulting nanoparticles were evaluated using dynamic light scattering (DLS). The CS: TPP ratio of 4:1, with an average hydrodynamic diameter (DHP) of (195 ± 10) nm and a zeta potential of (51 ± 1) mV, was identified as the most suitable for further analysis. The characterization of NPs by Transmission Electron Microscope (TEM) and atomic force microscopy (AFM) revealed diameters of (65 ± 14) nm and (102 ± 18) nm, respectively. Notably, CSNPs exhibited significant aggregation during centrifugation and lyophilization, leading to diameter increases of up to 285% as measured by AFM. The antibacterial activity of CSNPs against Staphylococcus aureus and Escherichia coli was assessed using the resazurin assay. It was found that CSNPs not subjected to centrifugation, freezing, and lyophilization retained their antimicrobial activity. In contrast, those that underwent these processes lost their efficacy, likely due to aggregation and destabilization of the system. This study presents a straightforward and effective protocol for encapsulating sensitive active agents and synthesizing chitosan nanoparticles, a potential system with significant implications in the fight against antibiotic resistance. Fil: Des Bouillons Gamboa, Rosvin E.. Laboratorio Nacional de Nanotecnología; Costa Rica. Tecnológico de Costa Rica; Costa Rica Fil: Montes de Oca, Gabriela. Laboratorio Nacional de Nanotecnología; Costa Rica Fil: Baudrit, Jose Roberto Vega. Laboratorio Nacional de Nanotecnología; Costa Rica Fil: Ríos Duarte, Liz Carolina. Universidad Autonoma de Asuncion.; Paraguay Fil: Lopretti, Mary. Universidad de la República; Uruguay Fil: Rentería Urquiza, Maite. Universidad de Guadalajara; México Fil: Zúñiga Umaña, Juan Miguel. Universidad de Guadalajara; México Fil: Barreiro, Filomena. Instituto Politécnico de Bragança.; Portugal Fil: Vazquez, Patricia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Ciencias Aplicadas "Dr. Jorge J. Ronco". Universidad Nacional de la Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Ciencias Aplicadas; Argentina |
description |
In the face of a pressing global issue-the escalating threat of antibiotic resistance-the development of new antimicrobial agents is urgent. Nanotechnology, with its innovative approach, emerges as a promising solution to enhance the efficacy of these agents and combat the challenge of microbial resistance. Chitosan nanoparticles (CSNPs) stand out in biomedical applications, particularly in the controlled release of antibiotics, with their unique properties such as biocompatibility, stability, biodegradability, non-toxicity, and simple synthesis processes suitable for sensitive molecules. This study synthesized CSNPs using the ionotropic gelation method, with tripolyphosphate (TPP) as the crosslinking agent. Various CS: TPP ratios (6:1, 5:1, 4:1, 3:1, 2:1) were tested, and the resulting nanoparticles were evaluated using dynamic light scattering (DLS). The CS: TPP ratio of 4:1, with an average hydrodynamic diameter (DHP) of (195 ± 10) nm and a zeta potential of (51 ± 1) mV, was identified as the most suitable for further analysis. The characterization of NPs by Transmission Electron Microscope (TEM) and atomic force microscopy (AFM) revealed diameters of (65 ± 14) nm and (102 ± 18) nm, respectively. Notably, CSNPs exhibited significant aggregation during centrifugation and lyophilization, leading to diameter increases of up to 285% as measured by AFM. The antibacterial activity of CSNPs against Staphylococcus aureus and Escherichia coli was assessed using the resazurin assay. It was found that CSNPs not subjected to centrifugation, freezing, and lyophilization retained their antimicrobial activity. In contrast, those that underwent these processes lost their efficacy, likely due to aggregation and destabilization of the system. This study presents a straightforward and effective protocol for encapsulating sensitive active agents and synthesizing chitosan nanoparticles, a potential system with significant implications in the fight against antibiotic resistance. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-11 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/264981 Des Bouillons Gamboa, Rosvin E.; Montes de Oca, Gabriela; Baudrit, Jose Roberto Vega; Ríos Duarte, Liz Carolina; Lopretti, Mary; et al.; Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs; Frontiers Media; Frontiers in Chemistry; 12; 11-2024; 1-14 2296-2646 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/264981 |
identifier_str_mv |
Des Bouillons Gamboa, Rosvin E.; Montes de Oca, Gabriela; Baudrit, Jose Roberto Vega; Ríos Duarte, Liz Carolina; Lopretti, Mary; et al.; Synthesis of chitosan nanoparticles (CSNP): effect of CH-CH-TPP ratio on size and stability of NPs; Frontiers Media; Frontiers in Chemistry; 12; 11-2024; 1-14 2296-2646 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.frontiersin.org/articles/10.3389/fchem.2024.1469271/full info:eu-repo/semantics/altIdentifier/doi/10.3389/fchem.2024.1469271 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Frontiers Media |
publisher.none.fl_str_mv |
Frontiers Media |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842980552304492544 |
score |
13.004268 |