| 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. |