Differentiation of flavonoid glycoside isomers by using metal complexation and electrospray ionization mass spectrometry
Differentiation of flavonoid glycoside isomers by using metal complexation and electrospray ionization mass spectrometry
复制标题
DOI:
10.1016/j.jasms.2003.07.002
复制
发表时间:
2003-12-01
影响因子:
3.2
通讯作者:
Brodbelt, JS
中科院分区:
文献类型:
--
作者:
Pikulski, M;Brodbelt, JS
The elucidation of flavonoid isomers is accomplished by electrospray ionization tandem mass spectrometry (ESI-MS/MS) via formation and collisional activated dissociation (CAD) of metal/flavonoid complexes containing an auxiliary ligand. Addition of a metal salt and a suitable neutral auxiliary ligand to flavonoids in solution results in the formation of [M(II) (flavonoid-H) ligand](+) complexes by ESI which, upon collisional activated dissociation, often result in more distinctive fragmentation patterns than observed for conventional protonated or deprotonated flavonoids. Previously, 2,2'-bipyridine was used as an auxiliary ligand, and now we compare and explore the use of alternative pyridyl ligands, including 4,7-diphenyl-1,10-phenanthroline. Using this technique, three groups of flavonoid glycoside isomers are differentiated, including glycosides of apigenin, quercetin, and luteolin. (C) 2003 American Society for Mass Spectrometry.