Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films

Detalhes bibliográficos
Autor(a) principal: Pamela Coradi da Silva
Data de Publicação: 2023
Outros Autores: Larissa Aroca Colucci, Larissa Lea da Silva, Celso Molina, Marcelo Dutra Duque, Leticia Norma Carpentieri Rodrigues
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/210961
Resumo: In this study, orodispersible films formed from hydroxypropyl methylcellulose (HPMC) E6 (2, 2.5, and 3%) and plasticizers ((glycerin (Gly), propylene glycol (PP), or polyethylene glycol (PEG)), containing doxazosin mesylate, were prepared by the solvent casting method and characterized. Design of experiments (DoE) was used as a statistical tool to facilitate the interpretation of the experimental data and allow the identification of optimal levels of factors for maximum formulation performance. Differential scanning calorimetry (DSC) curves and X-ray powder diffraction (XRPD) diffractograms showed doxazosin mesylate amorphization, probably due to complexation with the polymer (HPMC E6), and the glass transition temperature of the polymer was reduced by adding a plasticizer. Fourier transformed infrared (FTIR) spectroscopy results showed that the chemical structure of doxazosin mesylate was preserved when introduced into the polymer matrix, and the plasticizers, glycerin and PEG, affected the polymer matrix with high intensity. The addition of plasticizers increased the elongation at break and adhesiveness (Gly > PEG > PP), confirming the greater plasticizer effect of Gly observed in DSC and FTIR studies. Greater transparency was observed for the orodispersible films prepared using PP. The addition of citric acid as a pH modifier was fundamental for the release of doxazosin mesylate, and the desirability formulation had a release profile similar to that of the reference product.
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spelling Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible filmsOrodispersible films; Design of experiments; Doxazosin mesylate; FTIR; Mechanical properties; Desirability functionIn this study, orodispersible films formed from hydroxypropyl methylcellulose (HPMC) E6 (2, 2.5, and 3%) and plasticizers ((glycerin (Gly), propylene glycol (PP), or polyethylene glycol (PEG)), containing doxazosin mesylate, were prepared by the solvent casting method and characterized. Design of experiments (DoE) was used as a statistical tool to facilitate the interpretation of the experimental data and allow the identification of optimal levels of factors for maximum formulation performance. Differential scanning calorimetry (DSC) curves and X-ray powder diffraction (XRPD) diffractograms showed doxazosin mesylate amorphization, probably due to complexation with the polymer (HPMC E6), and the glass transition temperature of the polymer was reduced by adding a plasticizer. Fourier transformed infrared (FTIR) spectroscopy results showed that the chemical structure of doxazosin mesylate was preserved when introduced into the polymer matrix, and the plasticizers, glycerin and PEG, affected the polymer matrix with high intensity. The addition of plasticizers increased the elongation at break and adhesiveness (Gly > PEG > PP), confirming the greater plasticizer effect of Gly observed in DSC and FTIR studies. Greater transparency was observed for the orodispersible films prepared using PP. The addition of citric acid as a pH modifier was fundamental for the release of doxazosin mesylate, and the desirability formulation had a release profile similar to that of the reference product.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-04-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/21096110.1590/s2175-97902023e21114Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21114Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e21114Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e211142175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/210961/194407https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessPamela Coradi da SilvaLarissa Aroca ColucciLarissa Lea da SilvaCelso MolinaMarcelo Dutra DuqueLeticia Norma Carpentieri Rodrigues2023-05-24T17:29:08Zoai:revistas.usp.br:article/210961Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-05-24T17:29:08Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
title Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
spellingShingle Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
Pamela Coradi da Silva
Orodispersible films; Design of experiments; Doxazosin mesylate; FTIR; Mechanical properties; Desirability function
title_short Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
title_full Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
title_fullStr Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
title_full_unstemmed Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
title_sort Mechanical, optical, and physicochemical properties of HPMC-based doxazosin mesylate orodispersible films
author Pamela Coradi da Silva
author_facet Pamela Coradi da Silva
Larissa Aroca Colucci
Larissa Lea da Silva
Celso Molina
Marcelo Dutra Duque
Leticia Norma Carpentieri Rodrigues
author_role author
author2 Larissa Aroca Colucci
Larissa Lea da Silva
Celso Molina
Marcelo Dutra Duque
Leticia Norma Carpentieri Rodrigues
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Pamela Coradi da Silva
Larissa Aroca Colucci
Larissa Lea da Silva
Celso Molina
Marcelo Dutra Duque
Leticia Norma Carpentieri Rodrigues
dc.subject.por.fl_str_mv Orodispersible films; Design of experiments; Doxazosin mesylate; FTIR; Mechanical properties; Desirability function
topic Orodispersible films; Design of experiments; Doxazosin mesylate; FTIR; Mechanical properties; Desirability function
description In this study, orodispersible films formed from hydroxypropyl methylcellulose (HPMC) E6 (2, 2.5, and 3%) and plasticizers ((glycerin (Gly), propylene glycol (PP), or polyethylene glycol (PEG)), containing doxazosin mesylate, were prepared by the solvent casting method and characterized. Design of experiments (DoE) was used as a statistical tool to facilitate the interpretation of the experimental data and allow the identification of optimal levels of factors for maximum formulation performance. Differential scanning calorimetry (DSC) curves and X-ray powder diffraction (XRPD) diffractograms showed doxazosin mesylate amorphization, probably due to complexation with the polymer (HPMC E6), and the glass transition temperature of the polymer was reduced by adding a plasticizer. Fourier transformed infrared (FTIR) spectroscopy results showed that the chemical structure of doxazosin mesylate was preserved when introduced into the polymer matrix, and the plasticizers, glycerin and PEG, affected the polymer matrix with high intensity. The addition of plasticizers increased the elongation at break and adhesiveness (Gly > PEG > PP), confirming the greater plasticizer effect of Gly observed in DSC and FTIR studies. Greater transparency was observed for the orodispersible films prepared using PP. The addition of citric acid as a pH modifier was fundamental for the release of doxazosin mesylate, and the desirability formulation had a release profile similar to that of the reference product.
publishDate 2023
dc.date.none.fl_str_mv 2023-04-14
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/210961
10.1590/s2175-97902023e21114
url https://www.revistas.usp.br/bjps/article/view/210961
identifier_str_mv 10.1590/s2175-97902023e21114
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/210961/194407
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21114
Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e21114
Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e21114
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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