A modified high-performance liquid chromatographic (HPLC) method for determ
ination of trans-resveratrol (resveratrol) in peanuts and peanut products h
as been developed. Resveratrol was extracted with acetonitrile-water (90/10
, v/v) by blending with diatomaceous earth at high speed followed by purifi
cation of an aliquot of the extract on a minicolumn packed with Al2O3-ODS (
C-18) mixture. The column was eluted with acetonitrile-water (90/10, v/v),
eluate was evaporated under nitrogen, and residue was dissolved in HPLC mob
ile phase. Resveratrol in an aliquot of purified extract was quantitated by
HPLC on silica gel with n-hexane-2-propanol-water-acetonitrile-acetic acid
(1050/270/17/5/1, v/v) as a mobile phase. The recovery of resveratrol adde
d to diatomaceous earth at 0.05 mu g/g was 98.95 +/- 17.79%; the recovery o
f the standard added to fresh peanuts (with 0.070 mu g/g natural level of r
esveratrol) at 0.50, 5.00, and 10.00 mu g/g was 117.23 +/- 8.87, 100.10 +/-
2.49, and 100.45 +/- 1.51%, respectively. The quantitation limit of resver
atrol in fresh peanuts was about 0.01 mu g/g. Roasted peanuts had the lowes
t content of resveratrol of 0.055 +/- 0.023 mu g/g (n = 21), while in peanu
t butter its concentration was significantly higher, 0.324 +/- 0.129 mu g/g
(n = 46), and boiled peanuts had the highest level of 5.138 +/- 2.849 mu g
/g (n = 12). Resveratrol content in commercial peanut products was similar
to the resveratrol content of the raw peanut fractions routinely used for m
aking them.