Isotopic effects on retention times of caffeine and its metabolites 1,3,7-trimethyluric acid, theophylline, theobromine and paraxanthine

被引:15
作者
Benchekroun, Y [1 ]
Dautraix, S [1 ]
Desage, M [1 ]
Brazier, JL [1 ]
机构
[1] INST SCI PHARMACEUT & BIOL LYON,LAB ETUD ANALYT & CINET MED,F-69373 LYON 08,FRANCE
来源
JOURNAL OF CHROMATOGRAPHY B | 1997年 / 688卷 / 02期
关键词
caffeine; 1,3,7-trimethyluric acid; dimethylxanthines; theophylline; theobromine; paraxanthine;
D O I
10.1016/S0378-4347(96)00323-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Physicochemical parameters that influence gas chromatographic separation are numerous. Consequently, isotope labelling, because it modifies physicochemical properties, can induce isotopic effects on retention time. Caffeine has been chosen to study this influence because as itself and its metabolites, it allows the preparation of different methylxanthine isotopomers and thus is one of the best models to study isotopic effects induced by stable isotope labelling. Using a caffeine molecule labelled with deuterium at different positions and rat hepatocytes to obtain metabolites, it was possible to study the influence of labelling on retention time [(14% cyanopropylphenyl)methylpolysiloxane] and to point out the role of each labelled site. It appears that isotopic effects induced by the labelling depend not only on the number of labelling atoms but also on whether this labelling is at position 1, 3 or 7 and, consequently, on the role of the labelled site on the function of the molecule.
引用
收藏
页码:245 / 254
页数:10
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