Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation
Autor(a) principal: | |
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Data de Publicação: | 2019 |
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/180900 |
Resumo: | The objective of the current study was to encapsulate flaxseed oil extracted from finely grounded flaxseed powder and determined for its fatty acids content by GC/FID. Ionotropic gelation method was used to form beads containing 40% flaxseed oil with vitamin E being used as an antioxidant agent. The study employed calcium chloride solution as crosslinking agent with a combination of sodium alginate and salep. The effect of polymer concentrations and calcium chloride concentration on the morphology, entrapment efficiency and oil release was studied. The encapsulation efficiency reached 93.46 ± 0.064% using 0.6% of salep and 2% sodium alginate with 0.3M calcium chloride gelling solution. In SGF medium, the matrix released only about 28.56% of the entrapped flaxseed oil after 2 hours. The rest of the oil then released in the SIF medium, continuing for up to 5 h to release 99.32% of the oil. |
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oai:revistas.usp.br:article/180900 |
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Brazilian Journal of Pharmaceutical Sciences |
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|
spelling |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelationFlaxseed oilSodium alginateSalepBeadsThe objective of the current study was to encapsulate flaxseed oil extracted from finely grounded flaxseed powder and determined for its fatty acids content by GC/FID. Ionotropic gelation method was used to form beads containing 40% flaxseed oil with vitamin E being used as an antioxidant agent. The study employed calcium chloride solution as crosslinking agent with a combination of sodium alginate and salep. The effect of polymer concentrations and calcium chloride concentration on the morphology, entrapment efficiency and oil release was studied. The encapsulation efficiency reached 93.46 ± 0.064% using 0.6% of salep and 2% sodium alginate with 0.3M calcium chloride gelling solution. In SGF medium, the matrix released only about 28.56% of the entrapped flaxseed oil after 2 hours. The rest of the oil then released in the SIF medium, continuing for up to 5 h to release 99.32% of the oil.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2019-12-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/18090010.1590/s2175-97902019000200261Brazilian Journal of Pharmaceutical Sciences; Vol. 55 (2019); e00261Brazilian Journal of Pharmaceutical Sciences; v. 55 (2019); e00261Brazilian Journal of Pharmaceutical Sciences; Vol. 55 (2019); e002612175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/180900/167945Copyright (c) 2019 Brazilian Journal of Pharmaceutical Scienceshttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessWissam, Zam Samer, Housheh 2021-01-19T16:47:29Zoai:revistas.usp.br:article/180900Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2021-01-19T16:47:29Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
title |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
spellingShingle |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation Wissam, Zam Flaxseed oil Sodium alginate Salep Beads |
title_short |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
title_full |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
title_fullStr |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
title_full_unstemmed |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
title_sort |
Encapsulation of flaxseed oil extract in alginate–salep system by ionic gelation |
author |
Wissam, Zam |
author_facet |
Wissam, Zam Samer, Housheh |
author_role |
author |
author2 |
Samer, Housheh |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Wissam, Zam Samer, Housheh |
dc.subject.por.fl_str_mv |
Flaxseed oil Sodium alginate Salep Beads |
topic |
Flaxseed oil Sodium alginate Salep Beads |
description |
The objective of the current study was to encapsulate flaxseed oil extracted from finely grounded flaxseed powder and determined for its fatty acids content by GC/FID. Ionotropic gelation method was used to form beads containing 40% flaxseed oil with vitamin E being used as an antioxidant agent. The study employed calcium chloride solution as crosslinking agent with a combination of sodium alginate and salep. The effect of polymer concentrations and calcium chloride concentration on the morphology, entrapment efficiency and oil release was studied. The encapsulation efficiency reached 93.46 ± 0.064% using 0.6% of salep and 2% sodium alginate with 0.3M calcium chloride gelling solution. In SGF medium, the matrix released only about 28.56% of the entrapped flaxseed oil after 2 hours. The rest of the oil then released in the SIF medium, continuing for up to 5 h to release 99.32% of the oil. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-12-09 |
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/180900 10.1590/s2175-97902019000200261 |
url |
https://www.revistas.usp.br/bjps/article/view/180900 |
identifier_str_mv |
10.1590/s2175-97902019000200261 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/180900/167945 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2019 Brazilian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2019 Brazilian Journal of Pharmaceutical Sciences http://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. 55 (2019); e00261 Brazilian Journal of Pharmaceutical Sciences; v. 55 (2019); e00261 Brazilian Journal of Pharmaceutical Sciences; Vol. 55 (2019); e00261 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_ |
1800222914545451008 |