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dc.contributor.author Kursinszki, László
dc.contributor.author Sarkozi A,
dc.contributor.author Kéry, Ágnes
dc.contributor.author Szőke, Éva
dc.date.accessioned 2016-02-12T19:31:03Z
dc.date.available 2016-02-12T19:31:03Z
dc.date.issued 2006
dc.identifier.citation pagination=131-135; journalVolume=63; journalTitle=CHROMATOGRAPHIA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3056
dc.identifier.uri doi:10.1365/s10337-006-0808-8
dc.description.abstract A new high-performance liquid chromatographic method has been developed for analysis of isoquinoline alkaloids in extracts of Chelidonium majus L. Samples were extracted with acidic methanol and the extracts were purified by solid-phase extraction on Supelclean LC-18 cartridges. Optimized conditions resulted in high recovery and reproducibility. Simultaneous determination of protopine, chelidonine, coptisine, sanguinarine, and berberine was performed by HPLC on a C-18 reversed-phase column. Use of the Luna C18(2) new-generation silica-based stationary phase and 14.7:18:67.3 (v/v) acetonitrile-methanol-30 mM ammonium formate, pH 2.80, as mobile phase resulted in excellent peak shapes. Validation proved the repeatability of the method was good and recovery was satisfactory. Lower limits of detection were 0.2 ng for coptisine, 0.4 ng for sanguinarine, and 0.5 ng, for protopine, chelidonine, and berberine.
dc.relation.ispartof urn:issn:0009-5893
dc.title Improved RP-HPLC method for analysis of isoquinoline alkaloids in extracts of Chelidonium majus
dc.type Journal Article
dc.date.updated 2016-02-01T13:32:51Z
dc.language.rfc3066 en
dc.identifier.mtmt 1131327
dc.identifier.wos 000239016200022
dc.contributor.department SE/GYTK/Farmakognózia Intézet
dc.contributor.institution Semmelweis Egyetem


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