HPLC AND GC-MS IDENTIFICATION OF THE MAJOR ORGANIC-CONSTITUENTS IN NEW-ZEALAND PROPOLIS

Citation
Kr. Markham et al., HPLC AND GC-MS IDENTIFICATION OF THE MAJOR ORGANIC-CONSTITUENTS IN NEW-ZEALAND PROPOLIS, Phytochemistry, 42(1), 1996, pp. 205-211
Citations number
21
Categorie Soggetti
Plant Sciences
Journal title
ISSN journal
00319422
Volume
42
Issue
1
Year of publication
1996
Pages
205 - 211
Database
ISI
SICI code
0031-9422(1996)42:1<205:HAGIOT>2.0.ZU;2-B
Abstract
The major organic constituents of New Zealand sourced propolis have be en identified and quantified in tincture solutions by a combination of HPLC and GC-mass spectrometry (MS). HPLC was the preferred method for the analysis of flavonoids because of their very low response factors in CC-MS. Flavonoid levels ranged from 30-40 mg ml(-1). A distinctive characteristic of the flavonoids in New Zealand propolis is the unusu ally high proportion (ca 70%) of dihydroflavonoids, e.g. pinocembrin, pinobanksin and pinobanksin 3-acetate. Nonflavonoid components analyse d by CC-MS comprised a range of aromatic compounds (3-7.5 mg ml(-1)), together with low levels (0.25-0.78 mg ml(-1)) of fatty acids. The for mer comprised mainly cinnamic acids and their esters, but also include d the rare 5-phenyl-trans-trans-2,4-pentadienoic acid and the new natu ral product, 5-phenyl-trans-3-pentenoic acid. Both were synthesized to confirm their identity.