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Cytochrome P450 1A2 (CYP1A2) plays an important role in drug metabolism. Caffeine (CAF) is converted into paraxanthine (PX) by this enzyme and is used as a xenobiotic substrate to determine the CYP1A2 phenotype in humans. A method for the quantification of CAF and PX in saliva was developed using liquid-liquid extraction with ethyl acetate and analysis with ultra-high-performance liquid chromatography. Peaks from CAF, PX and internal standard were resolved within 6min. The method was validated from 0.05 to 5μgmL(-1) CAF and 0.025-2.5μgmL(-1) PX. Inter- and intra-day accuracies ranged from 91.2 to 107.2% with precisions <13.5%. The limits of detection were 0.16 and 0.63 ngmL(-1) for PX and CAF, respectively. PX/CAF concentration ratios from volunteers were 0.26-1.09 with mean ratios of 0.78±0.26 and 0.38±0.10 for regular and light/non-coffee drinkers, respectively.

More information Original publication

DOI

10.1016/j.jchromb.2015.05.020

Type

Journal article

Publication Date

2015-07-15T00:00:00+00:00

Volume

995-996

Pages

70 - 73

Total pages

3

Keywords

CYP1A2, Caffeine, Paraxanthine, Phenotyping, Saliva, UHPLC, Caffeine, Chromatography, High Pressure Liquid, Cytochrome P-450 CYP1A2, Humans, Linear Models, Phenotype, Reproducibility of Results, Saliva, Sensitivity and Specificity, Theophylline