Cranberry proanthocyanidin oligomers were investigated using ultra performance liquid chromatography-ion mobility-high-resolution mass spectrometry (UPLC-IM-HRMS). A total of 304 individual A-type and B-type proanthocyanidins, including 40 trimers, 68 tetramers, 53 pentamers, 54 hexamers, 49 heptamers, 28 octamers, and 12 nonamers, were characterized. A-type proanthocyanidins appeared to dominate the cranberry proanthocyanidins. As the degree of polymerization increased, the abundance of molecules with multiple A-type double inter-flavan linkage or having doubly charged ions also increased. Under the same charge state, the drift times of proanthocyanidin ions increased with their degree of polymerization or the number of double inter-flavan linkages. For the same proanthocyanidin molecules, doubly charged ions had shorter drift times compared to their singly charged counterparts, which lead to separated trendlines in the ion mobility-mass plot. While consistent ion mobility was observed for most proanthocyanidins with the same degree of polymerization, coeluted isomeric ions of trimer and tetramer were detected by their unique drift times. Incorporation of ion mobility into HRMS proved to be of great value to characterize and analyze proanthocyanidins from complex sample matrices. Graphical abstract.
Keywords: Cranberry; Drift time; Ion mobility; Mass spectrometry; Proanthocyanidin.