Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies

Detalhes bibliográficos
Autor(a) principal: Colucci,Larissa Aroca
Data de Publicação: 2022
Outros Autores: Rodrigues,Leticia Norma Carpentieri
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Archives of Biology and Technology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100627
Resumo: Abstract Orally disintegrating films (ODFs) comprising hydroxypropyl methylcellulose (HPMC) E6 (2%, 2.5%, and 3%) and plasticizers (glycerin [Gly], propylene glycol [1], or polyethylene glycol [2]) containing CPT were prepared by the solvent casting method and characterized. The design of experiments (DoE) was used considering the amount of film-forming agent (HPMC) and the nature of the plasticizers as independent variables and thickness, mechanical properties, disintegration time, and dissolution efficiency as dependent variables. The best formulation was selected based on the desirability function (fD). Color analysis was performed using CIE-Lab coordinates. The films had a pH less than 4 and were thus suitable for maximum stability of CPT. The amount of HPMC E6 and the nature of the plasticizer play a critical role in the physical, mechanical, and physicochemical properties of the films. Principal component analysis and hierarchical cluster analysis revealed a more defined distinction of the ODFs according to their chromatic characteristics. ODFs prepared with Gly and PEG 400 were translucent, whereas the other films were transparent. DoE successfully facilitated the interpretation of the experimental data and allowed the identification of optimal values of the factors for maximum yield. The maximum value obtained for fD was 0.8520, corresponding to 2.0 - 2.5% of the polymer (HPMC E6), and PP as plasticizer. The best-fitting kinetics model for CPT release from the ODFs was the Korsmeyer-Peppas model. The results showed that orally disintegrating films can be a promising alternative for oral administration of captopril.
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spelling Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studiescaptoprildesign of experiments (DoE)desirability functionmechanical propertiesorally disintegrating film.Abstract Orally disintegrating films (ODFs) comprising hydroxypropyl methylcellulose (HPMC) E6 (2%, 2.5%, and 3%) and plasticizers (glycerin [Gly], propylene glycol [1], or polyethylene glycol [2]) containing CPT were prepared by the solvent casting method and characterized. The design of experiments (DoE) was used considering the amount of film-forming agent (HPMC) and the nature of the plasticizers as independent variables and thickness, mechanical properties, disintegration time, and dissolution efficiency as dependent variables. The best formulation was selected based on the desirability function (fD). Color analysis was performed using CIE-Lab coordinates. The films had a pH less than 4 and were thus suitable for maximum stability of CPT. The amount of HPMC E6 and the nature of the plasticizer play a critical role in the physical, mechanical, and physicochemical properties of the films. Principal component analysis and hierarchical cluster analysis revealed a more defined distinction of the ODFs according to their chromatic characteristics. ODFs prepared with Gly and PEG 400 were translucent, whereas the other films were transparent. DoE successfully facilitated the interpretation of the experimental data and allowed the identification of optimal values of the factors for maximum yield. The maximum value obtained for fD was 0.8520, corresponding to 2.0 - 2.5% of the polymer (HPMC E6), and PP as plasticizer. The best-fitting kinetics model for CPT release from the ODFs was the Korsmeyer-Peppas model. The results showed that orally disintegrating films can be a promising alternative for oral administration of captopril.Instituto de Tecnologia do Paraná - Tecpar2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100627Brazilian Archives of Biology and Technology v.65 2022reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/1678-4324-2022220073info:eu-repo/semantics/openAccessColucci,Larissa ArocaRodrigues,Leticia Norma Carpentierieng2022-09-06T00:00:00Zoai:scielo:S1516-89132022000100627Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2022-09-06T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false
dc.title.none.fl_str_mv Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
title Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
spellingShingle Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
Colucci,Larissa Aroca
captopril
design of experiments (DoE)
desirability function
mechanical properties
orally disintegrating film.
title_short Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
title_full Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
title_fullStr Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
title_full_unstemmed Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
title_sort Development of Orally Disintegrating Films HPMC-Based Containing Captopril: Mechanical, Optical and Physicochemical Studies
author Colucci,Larissa Aroca
author_facet Colucci,Larissa Aroca
Rodrigues,Leticia Norma Carpentieri
author_role author
author2 Rodrigues,Leticia Norma Carpentieri
author2_role author
dc.contributor.author.fl_str_mv Colucci,Larissa Aroca
Rodrigues,Leticia Norma Carpentieri
dc.subject.por.fl_str_mv captopril
design of experiments (DoE)
desirability function
mechanical properties
orally disintegrating film.
topic captopril
design of experiments (DoE)
desirability function
mechanical properties
orally disintegrating film.
description Abstract Orally disintegrating films (ODFs) comprising hydroxypropyl methylcellulose (HPMC) E6 (2%, 2.5%, and 3%) and plasticizers (glycerin [Gly], propylene glycol [1], or polyethylene glycol [2]) containing CPT were prepared by the solvent casting method and characterized. The design of experiments (DoE) was used considering the amount of film-forming agent (HPMC) and the nature of the plasticizers as independent variables and thickness, mechanical properties, disintegration time, and dissolution efficiency as dependent variables. The best formulation was selected based on the desirability function (fD). Color analysis was performed using CIE-Lab coordinates. The films had a pH less than 4 and were thus suitable for maximum stability of CPT. The amount of HPMC E6 and the nature of the plasticizer play a critical role in the physical, mechanical, and physicochemical properties of the films. Principal component analysis and hierarchical cluster analysis revealed a more defined distinction of the ODFs according to their chromatic characteristics. ODFs prepared with Gly and PEG 400 were translucent, whereas the other films were transparent. DoE successfully facilitated the interpretation of the experimental data and allowed the identification of optimal values of the factors for maximum yield. The maximum value obtained for fD was 0.8520, corresponding to 2.0 - 2.5% of the polymer (HPMC E6), and PP as plasticizer. The best-fitting kinetics model for CPT release from the ODFs was the Korsmeyer-Peppas model. The results showed that orally disintegrating films can be a promising alternative for oral administration of captopril.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100627
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132022000100627
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-4324-2022220073
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
dc.source.none.fl_str_mv Brazilian Archives of Biology and Technology v.65 2022
reponame:Brazilian Archives of Biology and Technology
instname:Instituto de Tecnologia do Paraná (Tecpar)
instacron:TECPAR
instname_str Instituto de Tecnologia do Paraná (Tecpar)
instacron_str TECPAR
institution TECPAR
reponame_str Brazilian Archives of Biology and Technology
collection Brazilian Archives of Biology and Technology
repository.name.fl_str_mv Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)
repository.mail.fl_str_mv babt@tecpar.br||babt@tecpar.br
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