ASSAY FOR THE (R)-ENANTIOMERS AND (S)-ENANTIOMERS OF SALSOLINOLS IN BIOLOGICAL SAMPLES AND FOODS WITH ION-PAIR HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING BETA-CYCLODEXTRIN AS A CHIRAL MOBILE-PHASE ADDITIVE

Citation
Yl. Deng et al., ASSAY FOR THE (R)-ENANTIOMERS AND (S)-ENANTIOMERS OF SALSOLINOLS IN BIOLOGICAL SAMPLES AND FOODS WITH ION-PAIR HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING BETA-CYCLODEXTRIN AS A CHIRAL MOBILE-PHASE ADDITIVE, Journal of chromatography B. Biomedical sciences and applications, 689(2), 1997, pp. 313-320
Citations number
21
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
ISSN journal
13872273
Volume
689
Issue
2
Year of publication
1997
Pages
313 - 320
Database
ISI
SICI code
0378-4347(1997)689:2<313:AFT(A(>2.0.ZU;2-Z
Abstract
A chromatographic procedure was devised for the quantitative determina tion of the enantiomers of salsolinol and N-methylsalsolinol, which ar e biologically important alkaloids. The enantiomers of salsolinol and N-methylsalsolinol were completely separated using beta-cyclodextrin i n a reversed-phase ion-pair system. The HPLC method was sensitive enou gh to detect the isoquinolines at a concentration less than 0.1 pmol p er injection. The presence of (R)- and (S)-salsolinol was confirmed in fermented foods and beverages, white N-methylsalsolinol was not detec ted. On the other hand, the (R)-enantiomers of both salsolinol and N-m ethylsalsolinol were found to predominate in the human brain.