C. Emenhiser et al., CAPABILITY OF A POLYMERIC C-30 STATIONARY-PHASE TO RESOLVE CIS-TRANS CAROTENOID ISOMERS IN REVERSED-PHASE LIQUID-CHROMATOGRAPHY, Journal of chromatography, 707(2), 1995, pp. 205-216
Citations number
40
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
A novel polymeric C-30 stationary phase was tested for its ability to
separate geometric isomers of six common carotenoids (lutein, zeaxanth
in, beta-cryptoxanthin, alpha-carotene, beta-carotene, and lycopene) p
repared by photoisomerization of all-trans standards. Resolution and t
entative identification of asymmetrical carotenoid isomers yielded the
13-cis, 13'-cis, all-trans, 9-cis, and 9'-cis isomers of both lutein
and ct-carotene, and the 15-cis, 13-cis/3'-cis, all-trans, 9-cis, and
9'-cis isomers of beta-cryptoxanthin. Among symmetrical carotenoids, t
he 15-cis, 13-cis, all-trans, and 9-cis isomers of both zeaxanthin and
beta-carotene were resolved and tentatively identified, and nineteen
geometric isomers of lycopene were separated. Separations were carried
out using Vydac 201TP54 and Suplex pkb-100 stationary phases for comp
arison; in all cases, the C-30 stationary phase gave superior resoluti
on and produced unique separations.