Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , |
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=S0103-50532010000800017 |
Resumo: | Our previous research found that the crude extract of Neo-T. siphonanthun exhibited an effective DPPH (1,1-diphenyl-2-picryhydrazyl) radical scavenging activity. In this study an online rapid screening method, high-performance liquid chromatography-radical scavenging detection-diode array detector-electrospray ionization mass spectrometry (HPLC-RSD- DAD-ESI/MS) system, was developed for screening individual antioxidants from the most active fraction. Accordingly, three isomeric derivatives were detected. The target active compounds were isolated by high-speed counter-current chromatography (HSCCC) with the purity over 99%, and were identified as luteolin-3'-O-β-D-glucopyranoside (1), luteolin-7-O-β-D-glucopyranoside (2) and luteolin-4'-O-β-D-glucopyranoside (3) by analysis of its off-line nuclear magnetic resonance (NMR) spectra. Antioxidant activity of three compounds was assessed by off-line DPPH assay, and all of them showed potent activity. |
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Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthunHPLC-RSD-DAD-ESI/MSradical scavengerflavonoidHSCCCNeo-Taraxacum siphonanthunOur previous research found that the crude extract of Neo-T. siphonanthun exhibited an effective DPPH (1,1-diphenyl-2-picryhydrazyl) radical scavenging activity. In this study an online rapid screening method, high-performance liquid chromatography-radical scavenging detection-diode array detector-electrospray ionization mass spectrometry (HPLC-RSD- DAD-ESI/MS) system, was developed for screening individual antioxidants from the most active fraction. Accordingly, three isomeric derivatives were detected. The target active compounds were isolated by high-speed counter-current chromatography (HSCCC) with the purity over 99%, and were identified as luteolin-3'-O-β-D-glucopyranoside (1), luteolin-7-O-β-D-glucopyranoside (2) and luteolin-4'-O-β-D-glucopyranoside (3) by analysis of its off-line nuclear magnetic resonance (NMR) spectra. Antioxidant activity of three compounds was assessed by off-line DPPH assay, and all of them showed potent activity.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000800017Journal of the Brazilian Chemical Society v.21 n.8 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010000800017info:eu-repo/semantics/openAccessJiang,XinyuShi,ShuyunZhang,YupingChen,Xiaoqingeng2011-10-14T00:00:00Zoai:scielo:S0103-50532010000800017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-10-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
title |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
spellingShingle |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun Jiang,Xinyu HPLC-RSD-DAD-ESI/MS radical scavenger flavonoid HSCCC Neo-Taraxacum siphonanthun |
title_short |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
title_full |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
title_fullStr |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
title_full_unstemmed |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
title_sort |
Excellent combination of HPLC-RSD-DAD-ESI/MS and HSCCC experiments to screen and identify radical scavengers from Neo-Taraxacum siphonanthun |
author |
Jiang,Xinyu |
author_facet |
Jiang,Xinyu Shi,Shuyun Zhang,Yuping Chen,Xiaoqing |
author_role |
author |
author2 |
Shi,Shuyun Zhang,Yuping Chen,Xiaoqing |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Jiang,Xinyu Shi,Shuyun Zhang,Yuping Chen,Xiaoqing |
dc.subject.por.fl_str_mv |
HPLC-RSD-DAD-ESI/MS radical scavenger flavonoid HSCCC Neo-Taraxacum siphonanthun |
topic |
HPLC-RSD-DAD-ESI/MS radical scavenger flavonoid HSCCC Neo-Taraxacum siphonanthun |
description |
Our previous research found that the crude extract of Neo-T. siphonanthun exhibited an effective DPPH (1,1-diphenyl-2-picryhydrazyl) radical scavenging activity. In this study an online rapid screening method, high-performance liquid chromatography-radical scavenging detection-diode array detector-electrospray ionization mass spectrometry (HPLC-RSD- DAD-ESI/MS) system, was developed for screening individual antioxidants from the most active fraction. Accordingly, three isomeric derivatives were detected. The target active compounds were isolated by high-speed counter-current chromatography (HSCCC) with the purity over 99%, and were identified as luteolin-3'-O-β-D-glucopyranoside (1), luteolin-7-O-β-D-glucopyranoside (2) and luteolin-4'-O-β-D-glucopyranoside (3) by analysis of its off-line nuclear magnetic resonance (NMR) spectra. Antioxidant activity of three compounds was assessed by off-line DPPH assay, and all of them showed potent activity. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-01-01 |
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=S0103-50532010000800017 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000800017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532010000800017 |
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.21 n.8 2010 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 |
_version_ |
1750318171123875840 |