A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/153783 |
Resumo: | Interpolyelectrolyte complexes, which constitute a type of polymeric material obtained through the selfassembly of oppositely charged polymers, exhibit interesting properties for use in the design of smart matrices for drug delivery. In the present study, a stoichiometric interpolyelectrolyte complex (SIPEC) composed of Eudragit E® and Eudragit® L100 was obtained at pH 6.0 and characterized and evaluated as a hydrophilic matrix for dexibuprofen. The formation of a SIPEC was monitored by ζ-potential measurements and characterized using infrared spectroscopy, thermal analysis, and scanning electron microscopy. The results indicated that a SIPEC obtained under these conditions can be used as a matrix for controlling the release of dexibuprofen and exhibit a pH-triggered release. |
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oai:revistas.usp.br:article/153783 |
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Brazilian Journal of Pharmaceutical Sciences |
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A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical propertiesInterpolyelectrolyte complexPharmacotechnical propertiesDexibuprofenControlled releaseHydrophillic matrixInterpolyelectrolyte complexes, which constitute a type of polymeric material obtained through the selfassembly of oppositely charged polymers, exhibit interesting properties for use in the design of smart matrices for drug delivery. In the present study, a stoichiometric interpolyelectrolyte complex (SIPEC) composed of Eudragit E® and Eudragit® L100 was obtained at pH 6.0 and characterized and evaluated as a hydrophilic matrix for dexibuprofen. The formation of a SIPEC was monitored by ζ-potential measurements and characterized using infrared spectroscopy, thermal analysis, and scanning electron microscopy. The results indicated that a SIPEC obtained under these conditions can be used as a matrix for controlling the release of dexibuprofen and exhibit a pH-triggered release.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2018-07-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/15378310.1590/s2175-9790201800021718Brazilian Journal of Pharmaceutical Sciences; Vol. 54 Núm. 2 (2018); e17183Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 2 (2018); e17183Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 2 (2018); e171832175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/153783/150173Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessMontaña, Jorge AndrésPerez, León DaríoBaena, Yolima2019-03-17T13:48:38Zoai:revistas.usp.br:article/153783Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2019-03-17T13:48:38Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
title |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
spellingShingle |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties Montaña, Jorge Andrés Interpolyelectrolyte complex Pharmacotechnical properties Dexibuprofen Controlled release Hydrophillic matrix |
title_short |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
title_full |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
title_fullStr |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
title_full_unstemmed |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
title_sort |
A pH-responsive drug delivery matrix from an interpolyelectrolyte complex: preparation and pharmacotechnical properties |
author |
Montaña, Jorge Andrés |
author_facet |
Montaña, Jorge Andrés Perez, León Darío Baena, Yolima |
author_role |
author |
author2 |
Perez, León Darío Baena, Yolima |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Montaña, Jorge Andrés Perez, León Darío Baena, Yolima |
dc.subject.por.fl_str_mv |
Interpolyelectrolyte complex Pharmacotechnical properties Dexibuprofen Controlled release Hydrophillic matrix |
topic |
Interpolyelectrolyte complex Pharmacotechnical properties Dexibuprofen Controlled release Hydrophillic matrix |
description |
Interpolyelectrolyte complexes, which constitute a type of polymeric material obtained through the selfassembly of oppositely charged polymers, exhibit interesting properties for use in the design of smart matrices for drug delivery. In the present study, a stoichiometric interpolyelectrolyte complex (SIPEC) composed of Eudragit E® and Eudragit® L100 was obtained at pH 6.0 and characterized and evaluated as a hydrophilic matrix for dexibuprofen. The formation of a SIPEC was monitored by ζ-potential measurements and characterized using infrared spectroscopy, thermal analysis, and scanning electron microscopy. The results indicated that a SIPEC obtained under these conditions can be used as a matrix for controlling the release of dexibuprofen and exhibit a pH-triggered release. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-07-26 |
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/153783 10.1590/s2175-9790201800021718 |
url |
https://www.revistas.usp.br/bjps/article/view/153783 |
identifier_str_mv |
10.1590/s2175-9790201800021718 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/153783/150173 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) |
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. 54 Núm. 2 (2018); e17183 Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 2 (2018); e17183 Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 2 (2018); e17183 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 |
_version_ |
1800222913708687360 |