Gellan gum microspheres crosslinked with trivalent ion: Effect of polymer and crosslinker concentrations on drug release and mucoadhesive properties
Main Author: | |
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Publication Date: | 2016 |
Other Authors: | , |
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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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 |
_version_ |
1834482747907768320 |