Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology

Detalhes bibliográficos
Autor(a) principal: Tolosa,Tatiana C.
Data de Publicação: 2018
Outros Autores: Rogez,Hervé, Silva,Evaldo M., Souza,Jesus N. S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018001202475
Resumo: This study aimed to optimize the acid hydrolysis of glycosylated flavonols, to apply the optimum conditions for hydrolyzing Inga edulis extract (IEE), rich in glycosylated flavonols, and evaluating its impact on the antioxidant capacity. To evaluate the influence of three independent variables on the aglycone obtained after the reaction, the response surface methodology was applied using myricetin-3-O-rhamnoside (M3R) as a pure compound. The phenolic compound profile and antioxidant capacity were determined by high-performance liquid chromatography (HPLC) and the Trolox-equivalent antioxidant capacity (TEAC) assay, respectively. The maximum content of the aglycone myricetin (81.15%) occurred with 2.5 M HCl at 75 ºC for 60 min. Under these conditions, the IEE produced the aglycones myricetin, quercetin and cyanidin. The TEAC values of the M3R samples and IEE before and after acid hydrolysis did not show significant differences (p > 0.05). These results suggest that the hydrolytic process is effective to produce aglycone flavonoids from leaf extracts of I. edulis, and probably for other plant extracts rich in M3R.
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spelling Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodologyphenolic aglyconeantioxidant capacityhydrolytic processInga edulisThis study aimed to optimize the acid hydrolysis of glycosylated flavonols, to apply the optimum conditions for hydrolyzing Inga edulis extract (IEE), rich in glycosylated flavonols, and evaluating its impact on the antioxidant capacity. To evaluate the influence of three independent variables on the aglycone obtained after the reaction, the response surface methodology was applied using myricetin-3-O-rhamnoside (M3R) as a pure compound. The phenolic compound profile and antioxidant capacity were determined by high-performance liquid chromatography (HPLC) and the Trolox-equivalent antioxidant capacity (TEAC) assay, respectively. The maximum content of the aglycone myricetin (81.15%) occurred with 2.5 M HCl at 75 ºC for 60 min. Under these conditions, the IEE produced the aglycones myricetin, quercetin and cyanidin. The TEAC values of the M3R samples and IEE before and after acid hydrolysis did not show significant differences (p > 0.05). These results suggest that the hydrolytic process is effective to produce aglycone flavonoids from leaf extracts of I. edulis, and probably for other plant extracts rich in M3R.Sociedade Brasileira de Química2018-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018001202475Journal of the Brazilian Chemical Society v.29 n.12 2018reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20180125info:eu-repo/semantics/openAccessTolosa,Tatiana C.Rogez,HervéSilva,Evaldo M.Souza,Jesus N. S.eng2018-11-26T00:00:00Zoai:scielo:S0103-50532018001202475Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2018-11-26T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
title Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
spellingShingle Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
Tolosa,Tatiana C.
phenolic aglycone
antioxidant capacity
hydrolytic process
Inga edulis
title_short Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
title_full Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
title_fullStr Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
title_full_unstemmed Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
title_sort Optimization of Acid Hydrolysis of Myricetin-3-O-rhamnoside Using Response Surface Methodology
author Tolosa,Tatiana C.
author_facet Tolosa,Tatiana C.
Rogez,Hervé
Silva,Evaldo M.
Souza,Jesus N. S.
author_role author
author2 Rogez,Hervé
Silva,Evaldo M.
Souza,Jesus N. S.
author2_role author
author
author
dc.contributor.author.fl_str_mv Tolosa,Tatiana C.
Rogez,Hervé
Silva,Evaldo M.
Souza,Jesus N. S.
dc.subject.por.fl_str_mv phenolic aglycone
antioxidant capacity
hydrolytic process
Inga edulis
topic phenolic aglycone
antioxidant capacity
hydrolytic process
Inga edulis
description This study aimed to optimize the acid hydrolysis of glycosylated flavonols, to apply the optimum conditions for hydrolyzing Inga edulis extract (IEE), rich in glycosylated flavonols, and evaluating its impact on the antioxidant capacity. To evaluate the influence of three independent variables on the aglycone obtained after the reaction, the response surface methodology was applied using myricetin-3-O-rhamnoside (M3R) as a pure compound. The phenolic compound profile and antioxidant capacity were determined by high-performance liquid chromatography (HPLC) and the Trolox-equivalent antioxidant capacity (TEAC) assay, respectively. The maximum content of the aglycone myricetin (81.15%) occurred with 2.5 M HCl at 75 ºC for 60 min. Under these conditions, the IEE produced the aglycones myricetin, quercetin and cyanidin. The TEAC values of the M3R samples and IEE before and after acid hydrolysis did not show significant differences (p > 0.05). These results suggest that the hydrolytic process is effective to produce aglycone flavonoids from leaf extracts of I. edulis, and probably for other plant extracts rich in M3R.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-01
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=S0103-50532018001202475
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018001202475
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20180125
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 Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.29 n.12 2018
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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