Ordered mesoporous silicas for potential applications in solid vaccine formulations

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Campo DCValoridioma
dc.contributorLab. Imunogenéticapt_BR
dc.contributorCurso de Especialização em Biotecnologia para Saúde – Vacinas e Biofármacospt_BR
dc.contributor(LBI) Lab. Imunoquímicapt_BR
dc.contributorLab. Imunogenéticapt_BR
dc.contributor.authorMiranda, Matheus C. R.pt_BR
dc.contributor.authorNunes, Carmen M.pt_BR
dc.contributor.authorSantos, Luana F.pt_BR
dc.contributor.authorCardoso, Jéssica Soarespt_BR
dc.contributor.authorTrezena, Aryene Góespt_BR
dc.contributor.authorRibeiro, Orlando Garciapt_BR
dc.contributor.authorSant'anna, Osvaldo Augustopt_BR
dc.contributor.authorDe Franco, Milene Tinopt_BR
dc.date.accessioned2024-01-23T13:29:35Z-
dc.date.available2024-01-23T13:29:35Z-
dc.date.issued2024pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/5235-
dc.description.abstractIn an effort to develop efficient vaccine formulations, the use of ordered mesoporous silica (SBA-15) as an antigen carrier has been investigated. SBA-15 has required properties such as high surface area and pore volume, including narrow pore size distribution to protect antigens inside its matrix. This study aimed to examine the impact of solvent removal methods, specifically freeze-drying and evaporation on the intrinsic properties of an immunogenic complex. The immunogenic complexes, synthesized and incorporated with BSA, were characterized by various physicochemical techniques. Small Angle X-ray Scattering measurements revealed the characteristic reflections associated to pure SBA-15, indicating the preservation of the silica mesostructured following BSA incorporation and the formation of BSA aggregates within the macropore region. Nitrogen Adsorption Isotherm measurements demonstrated a decrease in surface area and pore volume for all samples, indicating that the BSA was incorporated into the SBA-15 matrix. Fluorescence spectroscopy evidenced that the tryptophan residues in BSA inside SBA-15 or in solution displayed similar spectra, showing the preservation of the aromatic residues’ environment. The Circular Dichroism spectra of BSA in both conditions suggest the preservation of its native secondary structure after the encapsulation process. The immunogenic analysis with the detection of anti-BSA IgG did not give any significant difference between the non-dried, freeze-dried or evaporated groups. However, all groups containing BSA and SBA-15 showed results almost three times higher than the groups with pure BSA (control group). These facts indicate that none of the BSA incorporation methods interfered with the immunogenicity of the complex. In particular, the freeze-dried process is regularly used in the pharmaceutical industry, therefore its adequacy to produce immunogenic complexes was proved Furthermore, the results showed that SBA-15 increased the immunogenic activity of BSA.pt_BR
dc.description.sponsorship(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulopt_BR
dc.description.sponsorship(CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superiorpt_BR
dc.description.sponsorship(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológicopt_BR
dc.format.extent689-700pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofVaccinept_BR
dc.rightsRestricted accesspt_BR
dc.titleOrdered mesoporous silicas for potential applications in solid vaccine formulationspt_BR
dc.typeArticlept_BR
dc.identifier.doi10.1016/j.vaccine.2023.12.032pt_BR
dc.identifier.urlhttps://doi.org/10.1016/j.vaccine.2023.12.032pt_BR
dc.contributor.external(UNIFESP) Universidade Federal de São Paulopt_BR
dc.contributor.external(USP) Universidade de São Paulopt_BR
dc.identifier.citationvolume42pt_BR
dc.identifier.citationissue3pt_BR
dc.subject.keywordSBA-15pt_BR
dc.subject.keywordbovine serum albuminpt_BR
dc.subject.keywordsolid vaccinept_BR
dc.subject.keywordvaccine adjuvantpt_BR
dc.relation.ispartofabbreviatedVaccinept_BR
dc.identifier.citationabntv. 42, n. 3, p. 689-700, jan. 2024pt_BR
dc.identifier.citationvancouver2024 Jan; 42(3):689-700pt_BR
dc.contributor.butantanCardoso, Jéssica Soares|:Egresso|:Curso de Especialização em Biotecnologia para Saúde – Vacinas e Biofármacospt_BR
dc.contributor.butantanTrezena, Aryene Góes|:Pesquisador|:Lab. Imunogenéticapt_BR
dc.contributor.butantanRibeiro, Orlando Garcia|:Pesquisador|:Lab. Imunogenéticapt_BR
dc.contributor.butantanSant'anna, Osvaldo Augusto|:Pesquisador|:(LBI) Lab. Imunoquímicapt_BR
dc.contributor.butantanDe Franco, Milene Tino|:Pesquisador|:Lab. Imunogenéticapt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦17/17844-8pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦19/07007-07pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦19/08582-5pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦22/08360-5pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦22/01951-8pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦22/15698-2pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦19/19567-7pt_BR
dc.sponsorship.butantan(CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior¦¦23038.000776/201754pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
item.grantfulltextnone-
item.languageiso639-1English-
item.fulltextSem Texto completo-
item.openairetypeArticle-
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