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Evaluation of polyelectrolyte and emulsion covalent crosslink of chitosan for producing mesalasine loaded submicron particles

dc.contributor.authorLacerda, Gabriel José Silveira
dc.contributor.authorPiantino, Beatriz Lemos
dc.contributor.authorGonzaga, Edeilson Vitor
dc.contributor.authorNaves, Valéria de Moura Leite
dc.contributor.authorPedreiro, Liliane Neves [UNESP]
dc.contributor.authorGremião, Maria Palmira Daflon [UNESP]
dc.contributor.authorPereira, Gislaine Ribeiro
dc.contributor.authorCarvalho, Flávia Chiva
dc.contributor.institutionUNIFAL-MG
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T02:33:54Z
dc.date.available2020-12-12T02:33:54Z
dc.date.issued2019-01-01
dc.description.abstractThis study evaluates various techniques for producing mesalamine (5ASA)-loaded particles employing chitosan as a biopolymer: (1) the polyelectrolyte complexation of chitosan with phthalate hypromelose (HP), (2) the chemical crosslinking of chitosan with genipin and (3) the water-in-oil emulsion method associated with chemical crosslinking with genipin. Systems were characterized by dynamic light scattering, zeta potential (ζ), powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and a drug release profile. Method (1) was efficiently produced unloaded nanoparticles (491 nm, PdI=0.26 and ζ = 23.2), but the conditions for chitosan and HP cross-linking enhanced the precipitation of 5ASA. Method (2) caused the degradation of the drug. Method 3 produced sub-micron and microparticles, thereby varying the agitation method; 3 h magnetic agitation resulted in 2692 nm, Pdi = 0.6 and ζ = 46, while Ultra-Turrax, 5 min produced submicron particles (537 nm, PdI = 0.6). The percentage yield was approximately 50%, which is very satisfactory considering the impossibility of encapsulating 5ASA using other methods. FTIR showed the covalent interaction of chitosan and genipin. The drug release was rapid in acidic fluid, but in neutral pH a slower release was obtained in the initial stage, followed by rapid release, which may ensure the controlled release of 5ASA in the colon.en
dc.description.affiliationSchool of Pharmacy Federal University of Alfenas UNIFAL-MG
dc.description.affiliationSchool of Pharmaceutical Sciences State University of São Paulo State UNESP
dc.description.affiliationUnespSchool of Pharmaceutical Sciences State University of São Paulo State UNESP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipIdCAPES: 131476/2016-5
dc.description.sponsorshipIdCNPq: 454679/2014-9
dc.description.sponsorshipIdFAPEMIG: CDS APQ 00465/14
dc.identifierhttp://dx.doi.org/10.1590/s2175-97902019000217847
dc.identifier.citationBrazilian Journal of Pharmaceutical Sciences, v. 55.
dc.identifier.doi10.1590/s2175-97902019000217847
dc.identifier.issn2175-9790
dc.identifier.issn1984-8250
dc.identifier.scopus2-s2.0-85078357749
dc.identifier.urihttp://hdl.handle.net/11449/201492
dc.language.isoeng
dc.relation.ispartofBrazilian Journal of Pharmaceutical Sciences
dc.sourceScopus
dc.subjectChemical cross-linking
dc.subjectChitosan
dc.subjectEmulsion method
dc.subjectMesalazine
dc.subjectPolyelectrolyte crosslinking
dc.titleEvaluation of polyelectrolyte and emulsion covalent crosslink of chitosan for producing mesalasine loaded submicron particlesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.departmentFármacos e Medicamentos - FCFpt

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