Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties

Bibliographic Details
Main Author: Boni, Fernanda Isadora [UNESP]
Publication Date: 2016
Other Authors: Prezotti, Fab�ola Garavello [UNESP], Cury, Beatriz Stringhetti Ferreira [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.3109/03639045.2015.1125915
http://hdl.handle.net/11449/174102
Summary: Gellan gum microspheres were obtained by ionotropic gelation technique, using the trivalent ion Al3+. The percentage of entrapment efficiency ranged from 48.76 to 87.52% and 22 randomized full factorial design demonstrated that both the increase of polymer concentration and the decrease of crosslinker concentration presented a positive effect in the amount of encapsulated drug. Microspheres size and circularity ranged from 700.17 to 938.32 �m and from 0.641 to 0.796 �m, respectively. The increase of polymer concentration (1-2%) and crosslinker concentration (3-5%) led to the enlargement of particle size and circularity. However, the association of increased crosslinker concentration and reduced polymer content made the particles more irregular. In vitro and ex vivo tests evidenced the high mucoadhesiveness of microspheres. The high liquid uptake ability of the microspheres was demonstrated and the pH variation did not affect this parameter. Drug release was pH dependent, with low release rates in acid pH (42.40% and 44.93%) and a burst effect in phosphate buffer pH (7.4). The Weibull model had the best correlation with the drug release data, demonstrating that the release process was driven by a complex mechanism involving the erosion and swelling of the matrix or by non-Fickian diffusion.
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spelling Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive propertiesColonic drug deliveryDissolution testIonotropic gelationMucoadhesionMultiparticulate systemGellan gum microspheres were obtained by ionotropic gelation technique, using the trivalent ion Al3+. The percentage of entrapment efficiency ranged from 48.76 to 87.52% and 22 randomized full factorial design demonstrated that both the increase of polymer concentration and the decrease of crosslinker concentration presented a positive effect in the amount of encapsulated drug. Microspheres size and circularity ranged from 700.17 to 938.32 �m and from 0.641 to 0.796 �m, respectively. The increase of polymer concentration (1-2%) and crosslinker concentration (3-5%) led to the enlargement of particle size and circularity. However, the association of increased crosslinker concentration and reduced polymer content made the particles more irregular. In vitro and ex vivo tests evidenced the high mucoadhesiveness of microspheres. The high liquid uptake ability of the microspheres was demonstrated and the pH variation did not affect this parameter. Drug release was pH dependent, with low release rates in acid pH (42.40% and 44.93%) and a burst effect in phosphate buffer pH (7.4). The Weibull model had the best correlation with the drug release data, demonstrating that the release process was driven by a complex mechanism involving the erosion and swelling of the matrix or by non-Fickian diffusion.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Drugs and Pharmaceuticals School of Pharmaceutical Sciences S�o Paulo State University - UNESPDepartment of Drugs and Pharmaceuticals School of Pharmaceutical Sciences S�o Paulo State University - UNESPUniversidade Estadual Paulista (Unesp)Boni, Fernanda Isadora [UNESP]Prezotti, Fab�ola Garavello [UNESP]Cury, Beatriz Stringhetti Ferreira [UNESP]2018-12-11T17:09:20Z2018-12-11T17:09:20Z2016-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1283-1290application/pdfhttp://dx.doi.org/10.3109/03639045.2015.1125915Drug Development and Industrial Pharmacy, v. 42, n. 8, p. 1283-1290, 2016.1520-57620363-9045http://hdl.handle.net/11449/17410210.3109/03639045.2015.11259152-s2.0-850098273852-s2.0-85009827385.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDrug Development and Industrial Pharmacy0,5190,519info:eu-repo/semantics/openAccess2025-03-29T05:17:52Zoai:repositorio.unesp.br:11449/174102Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-03-29T05:17:52Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
title Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
spellingShingle Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
Boni, Fernanda Isadora [UNESP]
Colonic drug delivery
Dissolution test
Ionotropic gelation
Mucoadhesion
Multiparticulate system
title_short Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
title_full Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
title_fullStr Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
title_full_unstemmed Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
title_sort Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
author Boni, Fernanda Isadora [UNESP]
author_facet Boni, Fernanda Isadora [UNESP]
Prezotti, Fab�ola Garavello [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
author_role author
author2 Prezotti, Fab�ola Garavello [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Boni, Fernanda Isadora [UNESP]
Prezotti, Fab�ola Garavello [UNESP]
Cury, Beatriz Stringhetti Ferreira [UNESP]
dc.subject.por.fl_str_mv Colonic drug delivery
Dissolution test
Ionotropic gelation
Mucoadhesion
Multiparticulate system
topic Colonic drug delivery
Dissolution test
Ionotropic gelation
Mucoadhesion
Multiparticulate system
description Gellan gum microspheres were obtained by ionotropic gelation technique, using the trivalent ion Al3+. The percentage of entrapment efficiency ranged from 48.76 to 87.52% and 22 randomized full factorial design demonstrated that both the increase of polymer concentration and the decrease of crosslinker concentration presented a positive effect in the amount of encapsulated drug. Microspheres size and circularity ranged from 700.17 to 938.32 �m and from 0.641 to 0.796 �m, respectively. The increase of polymer concentration (1-2%) and crosslinker concentration (3-5%) led to the enlargement of particle size and circularity. However, the association of increased crosslinker concentration and reduced polymer content made the particles more irregular. In vitro and ex vivo tests evidenced the high mucoadhesiveness of microspheres. The high liquid uptake ability of the microspheres was demonstrated and the pH variation did not affect this parameter. Drug release was pH dependent, with low release rates in acid pH (42.40% and 44.93%) and a burst effect in phosphate buffer pH (7.4). The Weibull model had the best correlation with the drug release data, demonstrating that the release process was driven by a complex mechanism involving the erosion and swelling of the matrix or by non-Fickian diffusion.
publishDate 2016
dc.date.none.fl_str_mv 2016-01-01
2018-12-11T17:09:20Z
2018-12-11T17:09:20Z
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/10.3109/03639045.2015.1125915
Drug Development and Industrial Pharmacy, v. 42, n. 8, p. 1283-1290, 2016.
1520-5762
0363-9045
http://hdl.handle.net/11449/174102
10.3109/03639045.2015.1125915
2-s2.0-85009827385
2-s2.0-85009827385.pdf
url http://dx.doi.org/10.3109/03639045.2015.1125915
http://hdl.handle.net/11449/174102
identifier_str_mv Drug Development and Industrial Pharmacy, v. 42, n. 8, p. 1283-1290, 2016.
1520-5762
0363-9045
10.3109/03639045.2015.1125915
2-s2.0-85009827385
2-s2.0-85009827385.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Drug Development and Industrial Pharmacy
0,519
0,519
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1283-1290
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 repositoriounesp@unesp.br
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