Pharmacokinetics of gallic acid and its relative bioavailability from tea in healthy humans

Citation
S. Shahrzad et al., Pharmacokinetics of gallic acid and its relative bioavailability from tea in healthy humans, J NUTR, 131(4), 2001, pp. 1207-1210
Citations number
24
Categorie Soggetti
Food Science/Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF NUTRITION
ISSN journal
00223166 → ACNP
Volume
131
Issue
4
Year of publication
2001
Pages
1207 - 1210
Database
ISI
SICI code
0022-3166(200104)131:4<1207:POGAAI>2.0.ZU;2-L
Abstract
Gallic acid (GA), a food component that is especially abundant in tea, is a n antimutagenic, anticarcinogenic and anti-inflammatory agent. We conducted a study using acidum gallicum tablets that contained 10% GA and 90% glucos e and a black tea brew that contained 93% of its GA in free form to determi ne the pharmacokinetics and relative bioavailability of GA in healthy human s. After the administration of a single oral dose of acidum gallicum tablet s or tea teach containing 0.3 mmol GA) to 10 volunteers, plasma and urine s amples were collected over various time intervals. Concentrations of GA and its metabolite, 4-O-methylgallic acid (40MGA), were determined, and the ph armacokinetic parameters were calculated. GA from both the tablets and tea was rapidly absorbed and eliminated with mean half-lives of 1.19 +/- 0.07 a nd 1.06 +/- 0.06 h and mean maximum concentrations of 1.83 +/- 0.16 and 2.0 9 +/- 0.22 mu mol/L (plasma), respectively. After oral administration of th e tablets and black tea, 36.4 +/- 4.5 and 39.6 +/- 5.1% of the GA dose were extracted in urine as GA and 40MGA, respectively. The relative bioavailabi lity of GA from tea compared with that from the tablets was 1.06 +/- 0.26, showing that GA is as available from drinking tea as it is from swallowing tablets of GA.