Identification of the major constituents of Hypericum perforatum by LC/SPE/NMR and/or LC/MS

dc.contributor.authorTatsis, E. C.en
dc.contributor.authorBoeren, S.en
dc.contributor.authorExarchou, V.en
dc.contributor.authorTroganis, A. N.en
dc.contributor.authorVervoort, J.en
dc.contributor.authorGerothanassis, I. P.en
dc.date.accessioned2015-11-24T16:39:22Z
dc.date.available2015-11-24T16:39:22Z
dc.identifier.issn0031-9422-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8148
dc.rightsDefault Licence-
dc.subjecthypericum perforatumen
dc.subjectlc/spe/nmren
dc.subjectdereplicationen
dc.subjecthyperforinen
dc.subjecthyperfirinen
dc.subjectflavonoidsen
dc.subjectst-johns-worten
dc.subjectperformance liquid-chromatographyen
dc.subjectnuclear-magnetic-resonanceen
dc.subjectsolid-phase extractionen
dc.subjectdad-spe-nmren
dc.subjectmass-spectrometryen
dc.subjectphenolic compositionen
dc.subjectarray detectionen
dc.subjectplant-extractsen
dc.subjectgreek oreganoen
dc.titleIdentification of the major constituents of Hypericum perforatum by LC/SPE/NMR and/or LC/MSen
heal.abstractThe newly established hyphenated instrumentation of LC/DAD/SPE/NMR and LC/UV/(ESI)MS techniques have been applied for separation and structure verification of the major known constituents present in Greek Hypericum perforatum extracts. The chromatographic separation was performed on a C 18 column. Acetonitrile-water was used as a mobile phase. For the on-line NMR detection, the analytes eluted from column were trapped one by one onto separate SPE cartridges, and hereafter transported into the NMR flow-cell. LC/DAD/SPE/NMR and LC/UV/MS allowed the characterization of constituents of Greek H. perforatum, mainly naphtodianthrones (hypericin, pseudohypericin, protohypericin, protopseudohypericin), phloroglucinols (hyperforin, adhyperforin), flavonoids (quercetin, quercitrin, isoquercitrin, hyperoside, astilbin, miquelianin, I3,II8-biapigenin) and phenolic acids (chlorogenic acid, 3-O-coumaroylquinic acid). Two phloroglucinols (hyperfirin and adhyperfirin) were detected for the first time, which have been previously reported to be precursors in the biosynthesis of hyperforin and adhyperforin. (c) 2006 Elsevier Ltd. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.phytochem.2006.11.026-
heal.identifier.secondary<Go to ISI>://000244365800014-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0031942206007357/1-s2.0-S0031942206007357-main.pdf?_tid=027ead8c-3247-11e3-b481-00000aacb35d&acdnat=1381476811_8d32b54fde8d823044de711dc34559f4-
heal.journalNamePhytochemistryen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2007-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

Files

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.74 KB
Format:
Item-specific license agreed upon to submission
Description: