Chitosan nanoparticles as a modified diclofenac drug release system

Bibliographic Details
Main Author: Duarte Junior, Anivaldo Pereira
Publication Date: 2017
Other Authors: Tavares, Eraldo José Madureira, Alves, Taís Vanessa Gabbay, de Moura, Márcia Regina [UNESP], da Costa, Carlos Emmerson Ferreira, Silva Júnior, José Otávio Carréra, Ribeiro Costa, Roseane Maria
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1007/s11051-017-3968-6
http://hdl.handle.net/11449/175022
Summary: This study evaluated a modified nanostructured release system employing diclofenac as a drug model. Biodegradable chitosan nanoparticles were prepared with chitosan concentrations between 0.5 and 0.8% (w/v) by template polymerization method using methacrylic acid in aqueous solution. Chitosan-poly(methacrylic acid) (CS-PMAA) nanoparticles showed uniform size around 50–100 nm, homogeneous morphology, and spherical shape. Raw material and chitosan nanoparticles were characterized by thermal analysis, Fourier transform infrared spectroscopy (FT-IR), and transmission electron microscopy (TEM), confirming the interaction between chitosan and methacrylic acid during nanoparticles preparation. Diclofenac sorption on the chitosan nanoparticles surface was achieved by incubation in water/ethanol (1:1) drug solution in concentrations of 0.5 and 0.8 mg/mL. The diclofenac amount sorbed per gram of CS-PMAA nanoparticles, when in a 0.5 mg/mL sodium diclofenac solution, was as follows: 12.93, 15, 20.87, and 29.63 mg/g for CS-PMAA nanoparticles 0.5, 0.6, 0.7, and 0.8% (w/v), respectively. When a 0.8 mg/mL sodium diclofenac solution was used, higher sorption efficiencies were obtained: For CS-PMAA nanoparticles with chitosan concentrations of 0.5, 0.6, 0.7, and 0.8% (w/v), the sorption efficiencies were 33.39, 49.58, 55.23, and 67.2 mg/g, respectively. Diclofenac sorption kinetics followed a second-order kinetics. Drug release from nanoparticles occurred in a period of up to 48 h and obeyed Korsmeyer-Peppas model, which was characterized mainly by Fickian diffusion transport. [Figure not available: see fulltext.].
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spelling Chitosan nanoparticles as a modified diclofenac drug release systemBiopolymerChitosanDrug deliveryNanoparticleNanotechnologyPharmaceuticsThis study evaluated a modified nanostructured release system employing diclofenac as a drug model. Biodegradable chitosan nanoparticles were prepared with chitosan concentrations between 0.5 and 0.8% (w/v) by template polymerization method using methacrylic acid in aqueous solution. Chitosan-poly(methacrylic acid) (CS-PMAA) nanoparticles showed uniform size around 50–100 nm, homogeneous morphology, and spherical shape. Raw material and chitosan nanoparticles were characterized by thermal analysis, Fourier transform infrared spectroscopy (FT-IR), and transmission electron microscopy (TEM), confirming the interaction between chitosan and methacrylic acid during nanoparticles preparation. Diclofenac sorption on the chitosan nanoparticles surface was achieved by incubation in water/ethanol (1:1) drug solution in concentrations of 0.5 and 0.8 mg/mL. The diclofenac amount sorbed per gram of CS-PMAA nanoparticles, when in a 0.5 mg/mL sodium diclofenac solution, was as follows: 12.93, 15, 20.87, and 29.63 mg/g for CS-PMAA nanoparticles 0.5, 0.6, 0.7, and 0.8% (w/v), respectively. When a 0.8 mg/mL sodium diclofenac solution was used, higher sorption efficiencies were obtained: For CS-PMAA nanoparticles with chitosan concentrations of 0.5, 0.6, 0.7, and 0.8% (w/v), the sorption efficiencies were 33.39, 49.58, 55.23, and 67.2 mg/g, respectively. Diclofenac sorption kinetics followed a second-order kinetics. Drug release from nanoparticles occurred in a period of up to 48 h and obeyed Korsmeyer-Peppas model, which was characterized mainly by Fickian diffusion transport. [Figure not available: see fulltext.].Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Laboratory of Pharmaceutical Nanotechnology College of Pharmacy Federal University of ParáLaboratory R&D Pharmaceutical and Cosmetic College of Pharmacy Federal University of ParáBrazilian Agricultural Research Corporation Eastern Amazon Laboratory of AgrobusinessFaculdade de Engenharia de Ilha Solteira Departamento de Física e Química UNESP—Universidade Estadual PaulistaFaculty of Chemical Engineering Federal University of ParáFaculdade de Engenharia de Ilha Solteira Departamento de Física e Química UNESP—Universidade Estadual PaulistaUniversidade Federal do Pará (UFPA)Laboratory of AgrobusinessUniversidade Estadual Paulista (Unesp)Duarte Junior, Anivaldo PereiraTavares, Eraldo José MadureiraAlves, Taís Vanessa Gabbayde Moura, Márcia Regina [UNESP]da Costa, Carlos Emmerson FerreiraSilva Júnior, José Otávio CarréraRibeiro Costa, Roseane Maria2018-12-11T17:13:53Z2018-12-11T17:13:53Z2017-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1007/s11051-017-3968-6Journal of Nanoparticle Research, v. 19, n. 8, 2017.1572-896X1388-0764http://hdl.handle.net/11449/17502210.1007/s11051-017-3968-62-s2.0-850270148392-s2.0-85027014839.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Nanoparticle Research0,528info:eu-repo/semantics/openAccess2023-10-31T06:10:18Zoai:repositorio.unesp.br:11449/175022Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-31T06:10:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Chitosan nanoparticles as a modified diclofenac drug release system
title Chitosan nanoparticles as a modified diclofenac drug release system
spellingShingle Chitosan nanoparticles as a modified diclofenac drug release system
Duarte Junior, Anivaldo Pereira
Biopolymer
Chitosan
Drug delivery
Nanoparticle
Nanotechnology
Pharmaceutics
title_short Chitosan nanoparticles as a modified diclofenac drug release system
title_full Chitosan nanoparticles as a modified diclofenac drug release system
title_fullStr Chitosan nanoparticles as a modified diclofenac drug release system
title_full_unstemmed Chitosan nanoparticles as a modified diclofenac drug release system
title_sort Chitosan nanoparticles as a modified diclofenac drug release system
author Duarte Junior, Anivaldo Pereira
author_facet Duarte Junior, Anivaldo Pereira
Tavares, Eraldo José Madureira
Alves, Taís Vanessa Gabbay
de Moura, Márcia Regina [UNESP]
da Costa, Carlos Emmerson Ferreira
Silva Júnior, José Otávio Carréra
Ribeiro Costa, Roseane Maria
author_role author
author2 Tavares, Eraldo José Madureira
Alves, Taís Vanessa Gabbay
de Moura, Márcia Regina [UNESP]
da Costa, Carlos Emmerson Ferreira
Silva Júnior, José Otávio Carréra
Ribeiro Costa, Roseane Maria
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do Pará (UFPA)
Laboratory of Agrobusiness
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Duarte Junior, Anivaldo Pereira
Tavares, Eraldo José Madureira
Alves, Taís Vanessa Gabbay
de Moura, Márcia Regina [UNESP]
da Costa, Carlos Emmerson Ferreira
Silva Júnior, José Otávio Carréra
Ribeiro Costa, Roseane Maria
dc.subject.por.fl_str_mv Biopolymer
Chitosan
Drug delivery
Nanoparticle
Nanotechnology
Pharmaceutics
topic Biopolymer
Chitosan
Drug delivery
Nanoparticle
Nanotechnology
Pharmaceutics
description This study evaluated a modified nanostructured release system employing diclofenac as a drug model. Biodegradable chitosan nanoparticles were prepared with chitosan concentrations between 0.5 and 0.8% (w/v) by template polymerization method using methacrylic acid in aqueous solution. Chitosan-poly(methacrylic acid) (CS-PMAA) nanoparticles showed uniform size around 50–100 nm, homogeneous morphology, and spherical shape. Raw material and chitosan nanoparticles were characterized by thermal analysis, Fourier transform infrared spectroscopy (FT-IR), and transmission electron microscopy (TEM), confirming the interaction between chitosan and methacrylic acid during nanoparticles preparation. Diclofenac sorption on the chitosan nanoparticles surface was achieved by incubation in water/ethanol (1:1) drug solution in concentrations of 0.5 and 0.8 mg/mL. The diclofenac amount sorbed per gram of CS-PMAA nanoparticles, when in a 0.5 mg/mL sodium diclofenac solution, was as follows: 12.93, 15, 20.87, and 29.63 mg/g for CS-PMAA nanoparticles 0.5, 0.6, 0.7, and 0.8% (w/v), respectively. When a 0.8 mg/mL sodium diclofenac solution was used, higher sorption efficiencies were obtained: For CS-PMAA nanoparticles with chitosan concentrations of 0.5, 0.6, 0.7, and 0.8% (w/v), the sorption efficiencies were 33.39, 49.58, 55.23, and 67.2 mg/g, respectively. Diclofenac sorption kinetics followed a second-order kinetics. Drug release from nanoparticles occurred in a period of up to 48 h and obeyed Korsmeyer-Peppas model, which was characterized mainly by Fickian diffusion transport. [Figure not available: see fulltext.].
publishDate 2017
dc.date.none.fl_str_mv 2017-08-01
2018-12-11T17:13:53Z
2018-12-11T17:13:53Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s11051-017-3968-6
Journal of Nanoparticle Research, v. 19, n. 8, 2017.
1572-896X
1388-0764
http://hdl.handle.net/11449/175022
10.1007/s11051-017-3968-6
2-s2.0-85027014839
2-s2.0-85027014839.pdf
url http://dx.doi.org/10.1007/s11051-017-3968-6
http://hdl.handle.net/11449/175022
identifier_str_mv Journal of Nanoparticle Research, v. 19, n. 8, 2017.
1572-896X
1388-0764
10.1007/s11051-017-3968-6
2-s2.0-85027014839
2-s2.0-85027014839.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Nanoparticle Research
0,528
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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