Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5134858 | Journal of Chromatography A | 2017 | 8 Pages |
â¢The ethanol extract of L. origanoides was analyzed by HPLC-UV-HRMSn and seven major compounds were identified.â¢HSCCC was used as a preparative tool for the pre-fractionation of the ethanol extract of L. origanoides.â¢By using a generic solvent system an enriched flavonoid fraction was obtained.â¢Zic-HILIC, monolithic and particulate RP18 were studied for HPLC-UV-HRMSn analyses of flavonoids.â¢By this approach, twelve compounds were further identified in addition to the seven major ones.
Lippia origanoides (Verbenaceae) is an important Brazilian medicinal plant, also used for culinary purposes. Most chemical studies with this plant have been focused on its volatile composition. In this work, we combined High-Speed Counter-current Chromatography (HSCCC) and High Performance Liquid Chromatography coupled to Ultra Violet detection and High Resolution Mass Spectrometry (HPLC-UV-HRMSn) methodologies to access the non-volatile chemical composition of L. origanoides. The crude ethanol extract of L. origanoides (LOEF) was first analyzed by HPLC-UV-HRMSn and allowed the identification of 7 major compounds. Among them, eriodictyol, naringenin and pinocembrin, were determined and are phytochemical markers of this plant. However, owing to the complexity of this plant matrix, LOEF was fractionated by HSCCC (hexane-ethanol-water, 4:3:1) as a tool for preparative pre-purification, affording a flavonoid-rich fraction. A column screening with the chromatographic stationary phases ZIC-HILIC, monolithic and particulate RP18 was performed. The best column separation was achieved with a Purospher STAR RP18e, which was used for HPLC-DAD-HRMSn studies. By this approach 12 compounds were further identified in addition to the major ones identified in the raw extract. Two of them, 6,8-di-C-hexosyl-luteolin and 6,8-di-C-glucosyl-apigenin, are being reported for the first time in the family Verbenaceae. This work shows the integration of HSCCC as a preparative tool for the fractionation and purification of natural products from a complex plant extract with other analytical techniques, with the purpose of showing each technique's potential.