Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate

Detalhes bibliográficos
Autor(a) principal: Carbinatto, Fernanda M. [UNESP]
Data de Publicação: 2012
Outros Autores: Castro, Ana Doris de [UNESP], Cury, Beatriz Stringhetti Ferreira [UNESP], Magalhaes, Alvicler, Evangelista, Raul Cesar [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.ijpharm.2011.11.042
http://hdl.handle.net/11449/8070
Resumo: Pectin-high amylose starch mixtures (1:4; 1:1; 4:1) were cross-linked at different degrees and characterized by rheological, thermal, X-ray diffraction and NMR analyses. For comparison, samples without cross-linker addition were also prepared and characterized. Although all samples behaved as gels, the results evidenced that the phosphorylation reaction promotes the network strengthening, resulting in covalent gels (highest critical stress, G' and recovery %). Likewise, cross-linked samples presented the highest thermal stability. However, alkaline treatment without cross-linker allowed a structural reorganization of samples, as they also behaved as covalent gels, but weaker than those gels from cross-linked samples, and presented higher thermal stability than the physical mixtures. X-ray diffractograms also evidenced the occurrence of physical and chemical modifications due to the cross-linking process and indicated that samples without cross-linker underwent some structural reorganization, resulting in a decrease of crystallinity. The chemical shift of resonance signals corroborates the occurrence of structural modifications by both alkaline treatment and cross-linking reaction. (C) 2011 Elsevier B.V. All rights reserved.
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spelling Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphateHigh amylose starchPectinCross-linkingThermal analysisRheologyX-ray diffractionPectin-high amylose starch mixtures (1:4; 1:1; 4:1) were cross-linked at different degrees and characterized by rheological, thermal, X-ray diffraction and NMR analyses. For comparison, samples without cross-linker addition were also prepared and characterized. Although all samples behaved as gels, the results evidenced that the phosphorylation reaction promotes the network strengthening, resulting in covalent gels (highest critical stress, G' and recovery %). Likewise, cross-linked samples presented the highest thermal stability. However, alkaline treatment without cross-linker allowed a structural reorganization of samples, as they also behaved as covalent gels, but weaker than those gels from cross-linked samples, and presented higher thermal stability than the physical mixtures. X-ray diffractograms also evidenced the occurrence of physical and chemical modifications due to the cross-linking process and indicated that samples without cross-linker underwent some structural reorganization, resulting in a decrease of crystallinity. The chemical shift of resonance signals corroborates the occurrence of structural modifications by both alkaline treatment and cross-linking reaction. (C) 2011 Elsevier B.V. All rights reserved.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)BZGUniv Estadual Paulista UNESP, Fac Ciencias Farmaceut, Dept Farmacos & Medicamentos, BR-14801902 Araraquara, SP, BrazilUniv Estadual Campinas UNICAMP, Inst Quim, BR-13083970 Campinas, SP, BrazilUniv Estadual Paulista UNESP, Fac Ciencias Farmaceut, Dept Farmacos & Medicamentos, BR-14801902 Araraquara, SP, BrazilCAPES: 2015/08FAPESP: 08/01901-3Elsevier B.V.Universidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Carbinatto, Fernanda M. [UNESP]Castro, Ana Doris de [UNESP]Cury, Beatriz Stringhetti Ferreira [UNESP]Magalhaes, AlviclerEvangelista, Raul Cesar [UNESP]2014-05-20T13:25:29Z2014-05-20T13:25:29Z2012-02-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article281-288application/pdfhttp://dx.doi.org/10.1016/j.ijpharm.2011.11.042International Journal of Pharmaceutics. Amsterdam: Elsevier B.V., v. 423, n. 2, p. 281-288, 2012.0378-5173http://hdl.handle.net/11449/807010.1016/j.ijpharm.2011.11.042WOS:000301157000015WOS000301157000015.pdf5361569184579557Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Pharmaceutics3.8621,172info:eu-repo/semantics/openAccess2024-01-08T06:21:05Zoai:repositorio.unesp.br:11449/8070Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-08T06:21:05Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
title Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
spellingShingle Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
Carbinatto, Fernanda M. [UNESP]
High amylose starch
Pectin
Cross-linking
Thermal analysis
Rheology
X-ray diffraction
title_short Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
title_full Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
title_fullStr Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
title_full_unstemmed Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
title_sort Physical properties of pectin-high amylose starch mixtures cross-linked with sodium trimetaphosphate
author Carbinatto, Fernanda M. [UNESP]
author_facet Carbinatto, Fernanda M. [UNESP]
Castro, Ana Doris de [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
Magalhaes, Alvicler
Evangelista, Raul Cesar [UNESP]
author_role author
author2 Castro, Ana Doris de [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
Magalhaes, Alvicler
Evangelista, Raul Cesar [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Campinas (UNICAMP)
dc.contributor.author.fl_str_mv Carbinatto, Fernanda M. [UNESP]
Castro, Ana Doris de [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
Magalhaes, Alvicler
Evangelista, Raul Cesar [UNESP]
dc.subject.por.fl_str_mv High amylose starch
Pectin
Cross-linking
Thermal analysis
Rheology
X-ray diffraction
topic High amylose starch
Pectin
Cross-linking
Thermal analysis
Rheology
X-ray diffraction
description Pectin-high amylose starch mixtures (1:4; 1:1; 4:1) were cross-linked at different degrees and characterized by rheological, thermal, X-ray diffraction and NMR analyses. For comparison, samples without cross-linker addition were also prepared and characterized. Although all samples behaved as gels, the results evidenced that the phosphorylation reaction promotes the network strengthening, resulting in covalent gels (highest critical stress, G' and recovery %). Likewise, cross-linked samples presented the highest thermal stability. However, alkaline treatment without cross-linker allowed a structural reorganization of samples, as they also behaved as covalent gels, but weaker than those gels from cross-linked samples, and presented higher thermal stability than the physical mixtures. X-ray diffractograms also evidenced the occurrence of physical and chemical modifications due to the cross-linking process and indicated that samples without cross-linker underwent some structural reorganization, resulting in a decrease of crystallinity. The chemical shift of resonance signals corroborates the occurrence of structural modifications by both alkaline treatment and cross-linking reaction. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2012
dc.date.none.fl_str_mv 2012-02-28
2014-05-20T13:25:29Z
2014-05-20T13:25:29Z
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/10.1016/j.ijpharm.2011.11.042
International Journal of Pharmaceutics. Amsterdam: Elsevier B.V., v. 423, n. 2, p. 281-288, 2012.
0378-5173
http://hdl.handle.net/11449/8070
10.1016/j.ijpharm.2011.11.042
WOS:000301157000015
WOS000301157000015.pdf
5361569184579557
url http://dx.doi.org/10.1016/j.ijpharm.2011.11.042
http://hdl.handle.net/11449/8070
identifier_str_mv International Journal of Pharmaceutics. Amsterdam: Elsevier B.V., v. 423, n. 2, p. 281-288, 2012.
0378-5173
10.1016/j.ijpharm.2011.11.042
WOS:000301157000015
WOS000301157000015.pdf
5361569184579557
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Pharmaceutics
3.862
1,172
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 281-288
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
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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