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.