Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends

Detalhes bibliográficos
Autor(a) principal: Boni, Fernanda Isadora [UNESP]
Data de Publicação: 2021
Outros Autores: Cury, Beatriz S. F. [UNESP], Ferreira, Natália Noronha [UNESP], Gremião, Maria Palmira Daflon [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/pharmaceutics13030407
http://hdl.handle.net/11449/208528
Resumo: Polymer blends of gellan gum (GG)/retrograded starch(RS) and GG/pectin (P) were cross-linked with calcium, aluminum, or both to prepare mucoadhesive microparticles as oral carriers of drugs or nano systems. Cross-linking with different cations promoted different effects on each blend, which can potentially be explored as novel strategies for modulating physical-chemical and mucoadhesive properties of microparticles. Particles exhibited spherical shapes, diameters from 888 to 1764 µm, and span index values lower than 0.5. Blends of GG: P cross-linked with aluminum resulted in smaller particles than those obtained by calcium cross-linking. GG: RS particles exhibited larger sizes, but cross-linking this blend with calcium promoted diameter reduction. The uptake rates of acid medium were lower than phosphate buffer (pH 6.8), especially GG: RS based particles cross-linked with calcium. On the other hand, particles based on GG: P cross-linked with calcium absorbed the highest volume of acid medium. The percentage of systems erosion was higher in acid medium, but apparently occurred in the outermost layer of the particle. In pH 6.8, erosion was lower, but caused expressive swelling of the matrixes. Calcium cross-linking of GG: RS promoted a significantly reduction on enzymatic degradation at both pH 1.2 and 6.8, which is a promising feature that can provide drug protection against premature degradation in the stomach. In contrast, GG: P microparticles cross-linked with calcium suffered high degradation at both pH values, an advantageous feature for quickly releasing drugs at different sites of the gastrointestinal tract. The high mucoadhesive ability of the microparticles was evidenced at both pH values, and the Freundlich parameters indicated stronger particle-mucin interactions at pH 6.8.
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spelling Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blendsEnzymatic degradationErosionGellan gumLiquid uptakeMucoadhesionPectinRetrograded starchPolymer blends of gellan gum (GG)/retrograded starch(RS) and GG/pectin (P) were cross-linked with calcium, aluminum, or both to prepare mucoadhesive microparticles as oral carriers of drugs or nano systems. Cross-linking with different cations promoted different effects on each blend, which can potentially be explored as novel strategies for modulating physical-chemical and mucoadhesive properties of microparticles. Particles exhibited spherical shapes, diameters from 888 to 1764 µm, and span index values lower than 0.5. Blends of GG: P cross-linked with aluminum resulted in smaller particles than those obtained by calcium cross-linking. GG: RS particles exhibited larger sizes, but cross-linking this blend with calcium promoted diameter reduction. The uptake rates of acid medium were lower than phosphate buffer (pH 6.8), especially GG: RS based particles cross-linked with calcium. On the other hand, particles based on GG: P cross-linked with calcium absorbed the highest volume of acid medium. The percentage of systems erosion was higher in acid medium, but apparently occurred in the outermost layer of the particle. In pH 6.8, erosion was lower, but caused expressive swelling of the matrixes. Calcium cross-linking of GG: RS promoted a significantly reduction on enzymatic degradation at both pH 1.2 and 6.8, which is a promising feature that can provide drug protection against premature degradation in the stomach. In contrast, GG: P microparticles cross-linked with calcium suffered high degradation at both pH values, an advantageous feature for quickly releasing drugs at different sites of the gastrointestinal tract. The high mucoadhesive ability of the microparticles was evidenced at both pH values, and the Freundlich parameters indicated stronger particle-mucin interactions at pH 6.8.School of Pharmaceutical Science São Paulo State University (UNESP) Araraquara, Road Araraquara-Jaú, Km 01School of Pharmaceutical Science São Paulo State University (UNESP) Araraquara, Road Araraquara-Jaú, Km 01Universidade Estadual Paulista (Unesp)Boni, Fernanda Isadora [UNESP]Cury, Beatriz S. F. [UNESP]Ferreira, Natália Noronha [UNESP]Gremião, Maria Palmira Daflon [UNESP]2021-06-25T11:13:36Z2021-06-25T11:13:36Z2021-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/pharmaceutics13030407Pharmaceutics, v. 13, n. 3, 2021.1999-4923http://hdl.handle.net/11449/20852810.3390/pharmaceutics130304072-s2.0-85103134722Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPharmaceuticsinfo:eu-repo/semantics/openAccess2021-10-23T19:02:14Zoai:repositorio.unesp.br:11449/208528Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T19:02:14Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
title Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
spellingShingle Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
Boni, Fernanda Isadora [UNESP]
Enzymatic degradation
Erosion
Gellan gum
Liquid uptake
Mucoadhesion
Pectin
Retrograded starch
title_short Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
title_full Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
title_fullStr Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
title_full_unstemmed Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
title_sort Ionic cross-linking as a strategy tomodulate the properties of oral mucoadhesive microparticles based on polysaccharide blends
author Boni, Fernanda Isadora [UNESP]
author_facet Boni, Fernanda Isadora [UNESP]
Cury, Beatriz S. F. [UNESP]
Ferreira, Natália Noronha [UNESP]
Gremião, Maria Palmira Daflon [UNESP]
author_role author
author2 Cury, Beatriz S. F. [UNESP]
Ferreira, Natália Noronha [UNESP]
Gremião, Maria Palmira Daflon [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Boni, Fernanda Isadora [UNESP]
Cury, Beatriz S. F. [UNESP]
Ferreira, Natália Noronha [UNESP]
Gremião, Maria Palmira Daflon [UNESP]
dc.subject.por.fl_str_mv Enzymatic degradation
Erosion
Gellan gum
Liquid uptake
Mucoadhesion
Pectin
Retrograded starch
topic Enzymatic degradation
Erosion
Gellan gum
Liquid uptake
Mucoadhesion
Pectin
Retrograded starch
description Polymer blends of gellan gum (GG)/retrograded starch(RS) and GG/pectin (P) were cross-linked with calcium, aluminum, or both to prepare mucoadhesive microparticles as oral carriers of drugs or nano systems. Cross-linking with different cations promoted different effects on each blend, which can potentially be explored as novel strategies for modulating physical-chemical and mucoadhesive properties of microparticles. Particles exhibited spherical shapes, diameters from 888 to 1764 µm, and span index values lower than 0.5. Blends of GG: P cross-linked with aluminum resulted in smaller particles than those obtained by calcium cross-linking. GG: RS particles exhibited larger sizes, but cross-linking this blend with calcium promoted diameter reduction. The uptake rates of acid medium were lower than phosphate buffer (pH 6.8), especially GG: RS based particles cross-linked with calcium. On the other hand, particles based on GG: P cross-linked with calcium absorbed the highest volume of acid medium. The percentage of systems erosion was higher in acid medium, but apparently occurred in the outermost layer of the particle. In pH 6.8, erosion was lower, but caused expressive swelling of the matrixes. Calcium cross-linking of GG: RS promoted a significantly reduction on enzymatic degradation at both pH 1.2 and 6.8, which is a promising feature that can provide drug protection against premature degradation in the stomach. In contrast, GG: P microparticles cross-linked with calcium suffered high degradation at both pH values, an advantageous feature for quickly releasing drugs at different sites of the gastrointestinal tract. The high mucoadhesive ability of the microparticles was evidenced at both pH values, and the Freundlich parameters indicated stronger particle-mucin interactions at pH 6.8.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T11:13:36Z
2021-06-25T11:13:36Z
2021-03-01
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/10.3390/pharmaceutics13030407
Pharmaceutics, v. 13, n. 3, 2021.
1999-4923
http://hdl.handle.net/11449/208528
10.3390/pharmaceutics13030407
2-s2.0-85103134722
url http://dx.doi.org/10.3390/pharmaceutics13030407
http://hdl.handle.net/11449/208528
identifier_str_mv Pharmaceutics, v. 13, n. 3, 2021.
1999-4923
10.3390/pharmaceutics13030407
2-s2.0-85103134722
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pharmaceutics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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
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