dc.contributor.author |
Daruházi, Ágnes Emma |
|
dc.contributor.author |
Szarka, Szabolcs |
|
dc.contributor.author |
Héthelyi É, |
|
dc.contributor.author |
Simándi, Béla |
|
dc.contributor.author |
Gyurján I, |
|
dc.contributor.author |
Szőke, Éva |
|
dc.contributor.author |
Lemberkovics, Éva |
|
dc.date.accessioned |
2016-03-30T08:31:44Z |
|
dc.date.available |
2016-03-30T08:31:44Z |
|
dc.date.issued |
2008 |
|
dc.identifier |
54849436427 |
|
dc.identifier.citation |
pagination=S71-S76;
journalVolume=68;
journalIssueNumber=Suppl. 1;
journalTitle=CHROMATOGRAPHIA; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/3143 |
|
dc.identifier.uri |
doi:10.1365/s10337-008-0679-2 |
|
dc.description.abstract |
A GC-MS method has been developed for the qualitative analysis of sterol and triterpene (terpenoid) constituents of Ononis spinosa L. (spiny restharrow) root without derivatization. β-Sitosterol, campesterol, stigmasterol, stigmastan-3,5-diene sterol compounds and the triterpene derivatives β-amyrin and α-onocerin were identified. A validated GC-FID quantitative method was developed for measuring β-sitosterol, the main sterol component, in various extracts of this plant, obtained with organic solvents and by supercritical fluid extraction. The extracts were cleaned by saponifying and then the β-sitosterol was quantified in the non-saponifiable fractions by GC-FID with an internal standard. In addition, the relative concentrations of the other terpenoids were also determined. The β-sitosterol content in the non-saponifiable solvent extraction fractions was 0.19-5.5%, that of the supercritical fractions were 4.8-9.2%, depending on the experimental conditions. The hexane and the pilot scale SFE extracts were considered as main sources of terpenoids (71.8%; 93.3%, respectively). © 2008 Vieweg+Teubner | GWV Fachverlage GmbH. |
|
dc.relation.ispartof |
urn:issn:0009-5893 |
|
dc.title |
GC-MS identification and GC-FID quantitation of terpenoids in Ononidis spinosae Radix |
|
dc.type |
Journal Article |
|
dc.date.updated |
2016-02-26T10:42:54Z |
|
dc.language.rfc3066 |
en |
|
dc.identifier.mtmt |
1473336 |
|
dc.identifier.wos |
000262732400011 |
|
dc.contributor.department |
SE/GYTK/Farmakognózia Intézet |
|
dc.contributor.department |
Budapesti Műszaki és Gazdaságtudományi Egyetem |
|
dc.contributor.department |
BME/VBK/Kémiai és Környezeti Folyamatmérnöki Tanszék |
|
dc.contributor.institution |
Semmelweis Egyetem |
|
dc.contributor.institution |
Budapesti Műszaki és Gazdaságtudományi Egyetem |
|
dc.mtmt.swordnote |
Presented at: 7th Balaton Symposium on High-Performance Separation Methods, Siófok, Hungary, September 5–7, 2007. |
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