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Determination of Urinary Caffeine Metabolites as Biomarkers for Drug Metabolic Enzyme Activitiesopen access

Authors
Kim, Hyeong JunChoi, Min SunRehman, Shaheed UrJi, Young SeokYu, Jun SangNakamura, KatsunoriYoo, Hye Hyun
Issue Date
Aug-2019
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
caffeine; metabolites; phenotyping; CYP450; NAT; xanthine oxidase
Citation
Nutrients, v.11, no.8, pp.1 - 15
Indexed
SCIE
SCOPUS
Journal Title
Nutrients
Volume
11
Number
8
Start Page
1
End Page
15
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/2423
DOI
10.3390/nu11081947
ISSN
2072-6643
Abstract
Caffeine is commonly taken via the daily dietary consumption of caffeine-containing foods. The absorbed caffeine is metabolized to yield various metabolites by drug-metabolizing enzymes, and measuring the levels of each caffeine metabolite can provide useful information for evaluating the phenotypes of those enzymes. In this study, the urinary concentrations of caffeine and its 13 metabolites were determined, and the phenotypes of drug metabolic enzymes were investigated based on the caffeine metabolite ratios. Human urine samples were pretreated using solid phase extraction, and caffeine and its metabolites were analyzed using liquid chromatography-tandem mass spectrometry. Based on the urinary caffeine metabolite concentrations, the caffeine metabolite ratios were calculated for six human subjects at specified time points after caffeine intake. Variations in urinary metabolite levels among individuals and time points were reported. In addition, the resultant enzyme activities showed different patterns, depending on the metabolite ratio equations applied. However, some data presented a constant metabolite ratio range, irrespective of time points, even at pre-dose. This suggests the possibility of urinary caffeine metabolite analysis for routine clinical examination. These findings show that urinary caffeine and the metabolite analysis would be useful in evaluating metabolic phenotypes for personalized medicine.
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