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Registro Completo |
Biblioteca(s): |
Embrapa Amazônia Oriental. |
Data corrente: |
08/09/2017 |
Data da última atualização: |
20/05/2022 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
DUARTE JUNIOR, A. P.; TAVARES, E. J. M.; ALVES, T. V. G.; MOURA, M. R. de; COSTA, C. E. F. da; SILVA JÚNIOR, J. O. C.; COSTA, R. M. R. |
Afiliação: |
Anivaldo Pereira Duarte Junior, UFPA; ERALDO JOSE MADUREIRA TAVARES, CPATU; Taís Vanessa Gabbay Alves, UFPA; Márcia Regina de Moura, UNESP; Carlos Emmerson Ferreira da Costa, UFPA; José Otávio Carréra Silva Júnior, UFPA; Roseane Maria Ribeiro Costa, UFPA. |
Título: |
Chitosan nanoparticles as a modified diclofenac drug release system. |
Ano de publicação: |
2017 |
Fonte/Imprenta: |
Journal of Nanoparticle Research, v. 19, n. 8, article 274, 2017. |
DOI: |
10.1007/s11051-017-3968-6 |
Idioma: |
Inglês |
Conteúdo: |
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. MenosThis 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 o... Mostrar Tudo |
Palavras-Chave: |
Biopolímero; Nanopartícula; Nanotecnologia; Quitosana. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
Marc: |
LEADER 02347naa a2200253 a 4500 001 2075279 005 2022-05-20 008 2017 bl uuuu u00u1 u #d 024 7 $a10.1007/s11051-017-3968-6$2DOI 100 1 $aDUARTE JUNIOR, A. P. 245 $aChitosan nanoparticles as a modified diclofenac drug release system.$h[electronic resource] 260 $c2017 520 $aThis 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. 653 $aBiopolímero 653 $aNanopartícula 653 $aNanotecnologia 653 $aQuitosana 700 1 $aTAVARES, E. J. M. 700 1 $aALVES, T. V. G. 700 1 $aMOURA, M. R. de 700 1 $aCOSTA, C. E. F. da 700 1 $aSILVA JÚNIOR, J. O. C. 700 1 $aCOSTA, R. M. R. 773 $tJournal of Nanoparticle Research$gv. 19, n. 8, article 274, 2017.
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Registro original: |
Embrapa Amazônia Oriental (CPATU) |
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Registros recuperados : 107 | |
101. | | MOURA, M. R. de; AVENA-BUSTILLOS, R. J.; MCHUGH, T. H.; WOOD, D. F.; OTONI, C. G.; MATTOSO, L. H. C. Miniaturization of cellulose fibers and effect of addition on the mechanical and barrier properties of hydroxypropyl methylcellulose films. Journal of food engineering, Essex, v. 104, n. 1, p. 154-160, 2011.Tipo: Artigo em Periódico Indexado | Circulação/Nível: A - 1 |
Biblioteca(s): Embrapa Instrumentação. |
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102. | | PILON, L.; SPRICIGO, P. C.; MOURA, M. R. de; MIRANDA, M.; OHASHI, T. L.; MATTOSO, L. H. C.; FERREIRA, M. D. Microbiological quality of fresh-cut apple treated with chitosan nanoparticles-based edible coatings. In: WORLD CONGRESS OF FOOD SCIENCE AND TECHNOLOGY, 16.; LATIN AMERICAN SEMINAR OF FOOD SCIENCE AND TECHNOLOGY, 17., 2012, Foz do Iguaçu. Addressing global food security and wellness through food science and technology: abstracts. Foz do Iguaçu: [s.n.], 2012. 1 CD-ROM. IUFoST 2012.Tipo: Artigo em Anais de Congresso |
Biblioteca(s): Embrapa Instrumentação. |
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103. | | TAVARES, E. J. M.; PEREIRA, W. L. A.; VASCONCELOS, F.; FRACETO, L. F.; OLIVEIRA, M. E. C.; MOURA, M. R. de; MATTOSO, L. H. C.; AOUADA, F. A.; MELO, N. F. S. de; ALVES, R. M. Assessment of the citotoxicity and acute oral toxicity of a new spherical chitosan-polymethacrylic acid (CS-PMAA) nanoparticle In: INTERNATIONAL CONFERENCE ON FOOD AND AGRICULTURE APPLICATIONS OF NANOTECHNOLOGIES - NanoAgri, 2010, São Pedro, SP. [Anais?] São Pedro: Aptor Software, 2010. Editors: Caue Ribeiro, Odílio Benedito Garrido de Assis, Luiz Henrique Capparelli Mattoso, Sérgio Mascarenhas.Tipo: Artigo em Anais de Congresso |
Biblioteca(s): Embrapa Amazônia Oriental; Embrapa Instrumentação. |
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104. | | DUARTE JUNIOR, A. P.; TAVARES, E. J. M.; ALVES, T. V. G.; MOURA, M. R. de; COSTA, C. E. F. da; SILVA JÚNIOR, J. O. C.; COSTA, R. M. R. Chitosan nanoparticles as a modified diclofenac drug release system. Journal of Nanoparticle Research, v. 19, n. 8, article 274, 2017.Tipo: Artigo em Periódico Indexado | Circulação/Nível: A - 1 |
Biblioteca(s): Embrapa Amazônia Oriental. |
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105. | | DUARTE JUNIOR, A. P.; ALVES, T. V. G.; TAVARES, E. J. M.; MOURA, M. R. de; OLIVEIRA, M. E. C.; COSTA, C. E. F. da; COSTA, R. M. R.; SILVA JUNIOR, J. O. C. Caracterização térmica de nanopartículas de quitosana. In: CONGRESSO BRASILEIRO DE ANÁLISE TÉRMICA E CALORIMETRIA, 7., 2010, São Pedro. [Anais]. [São Paulo]: ABRATEC, 2010.Tipo: Artigo em Anais de Congresso |
Biblioteca(s): Embrapa Amazônia Oriental. |
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106. | | TAVARES, E. J. M.; PEREIRA, W. L. A.; AOUADA, F. A.; VASCONCELOS, F. de; MOURA, M. R. de; ALVES, R. M.; MATTOSO, L. H. C.; OLIVEIRA, M. E. C. Teste da toxicidade aguda oral de um novo hidrogel para liberação controlada de insumos agropecuários. In: WORKSHOP DA REDE DE NANOTECNOLOGIA APLICADA AO AGRONEGÓCIO, 5., 2009, São Carlos, SP. Anais... São Carlos, SP: Embrapa Instrumentação Agropecuária, 2009. p. 136-138. Editado por: Odílio Benedito Garrido de Assis, Wilson Tadeu Lopes da Silva, Luiz Henrique Capparelli Mattoso.Tipo: Artigo em Anais de Congresso / Nota Técnica |
Biblioteca(s): Embrapa Amazônia Oriental. |
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107. | | TAVARES, E. J. M.; PEREIRA, W. L. A.; AOUADA, F. A.; VASCONCELOS, F. de; MOURA, M. R. de; ALVES, R. M.; MATTOSO, L. H. C.; OLIVEIRA, M. E. C. Teste da toxicidade aguda oral de um novo hidrogel para liberação controlada de insumos agropecuários. In: WORKSHOP DA REDE DE NANOTECNOLOGIA APLICADA AO AGRONEGÓCIO, 5., 2009, São Carlos. Anais... São Carlos: Embrapa Instrumentação Agropecuária, 2009. p. 136-138. Editado por Odílio Benedito Garrido de Assis; Wilson Tadeu Lopes da Silva; Luiz Henrique Capparelli Mattoso.Tipo: Artigo em Anais de Congresso / Nota Técnica |
Biblioteca(s): Embrapa Instrumentação. |
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Registros recuperados : 107 | |
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Nenhum registro encontrado para a expressão de busca informada. |
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