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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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Embrapa Amazônia Oriental (CPATU) |
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| Acesso ao texto completo restrito à biblioteca da Embrapa Agroindústria Tropical. Para informações adicionais entre em contato com cnpat.biblioteca@embrapa.br. |
Registro Completo
Biblioteca(s): |
Embrapa Agroindústria Tropical. |
Data corrente: |
03/08/2017 |
Data da última atualização: |
20/11/2017 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
SOUSA, F. A.; NORONHA, V. T.; MACHADO, T. F.; SILVEIRA, J. V.; CUNHA, F. A.; FECHINE, P. B. A.; PAULA, A. J. |
Afiliação: |
FRANCISCO A. SOUSA, Grupo de Interfaces Sólido-Biológicas (SolBIN), Departamento de Física, Universidade Federal do Ceará.; VICTOR T. NORONHA, Grupo de Interfaces Sólido-Biológicas (SolBIN), Departamento de Física, Universidade Federal do Ceará; TEREZINHA FEITOSA MACHADO, CNPAT; JOSE V. SILVEIRA, Grupo de Química de Materiais Avançados (GQMAT), Departamento de Química Analítica e Físico-Química, Universidade Federal do Ceará.; FRANCISCO A. CUNHA, Grupo de Química de Materiais Avançados (GQMAT), Departamento de Química Analítica e Físico-Química, Universidade Federal do Ceará.; PIERRE B. A. FECHINE, Grupo de Química de Materiais Avançados (GQMAT), Departamento de Química Analítica e Físico-Química, Universidade Federal do Ceará.; AMAURI J. PAULA, Grupo de Interfaces Sólido-Biológicas (SolBIN), Departamento de Física, Universidade Federal do Ceará. |
Título: |
Silver nanocoatings at large length scales: Influence of the AgNPs morphology and capping agents on the coating chemical stability and antimicrobial effect. |
Ano de publicação: |
2017 |
Fonte/Imprenta: |
Journal of the Brazilian Chemical Society, v. 28, n. 9, p. 1639-1649, 2017. |
Idioma: |
Inglês |
Palavras-Chave: |
Image processing; Imagem de raio X; Large-field X-ray; Microscopia de varredura laser confocal; Microscopia eletrônica de varredura; Nanobiotechnology; Nanobiotecnologia; Processamento de imagens. |
Thesaurus NAL: |
confocal laser scanning microscopy; scanning electron microscopy. |
Categoria do assunto: |
-- |
Marc: |
LEADER 01060naa a2200301 a 4500 001 2073531 005 2017-11-20 008 2017 bl uuuu u00u1 u #d 100 1 $aSOUSA, F. A. 245 $aSilver nanocoatings at large length scales$bInfluence of the AgNPs morphology and capping agents on the coating chemical stability and antimicrobial effect.$h[electronic resource] 260 $c2017 650 $aconfocal laser scanning microscopy 650 $ascanning electron microscopy 653 $aImage processing 653 $aImagem de raio X 653 $aLarge-field X-ray 653 $aMicroscopia de varredura laser confocal 653 $aMicroscopia eletrônica de varredura 653 $aNanobiotechnology 653 $aNanobiotecnologia 653 $aProcessamento de imagens 700 1 $aNORONHA, V. T. 700 1 $aMACHADO, T. F. 700 1 $aSILVEIRA, J. V. 700 1 $aCUNHA, F. A. 700 1 $aFECHINE, P. B. A. 700 1 $aPAULA, A. J. 773 $tJournal of the Brazilian Chemical Society$gv. 28, n. 9, p. 1639-1649, 2017.
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