We established a method for using HPLC and diode-array ultraviolet scanning
to quantitate soy isoflavonoids in foods and in human plasma, urine, and b
reast milk. The analytes occurring as glycoside conjugates were hydrolyzed
enzymatically before HPLC analysis if extracted from biological matrices or
were subjected to direct HPLC analysis after extraction from foods. We mon
itored the isoflavones daidzein, genistein, glycitein, formononetin, and bi
ochanin-A and their mammalian metabolites equol and O-desmethylangolensin i
n human plasma, urine, and breast milk. Analytes were identified by absorba
nce patterns, fluorometric and electrochemical detection, and comparison wi
th internal and external standards. In addition, we identified analytes by
using gas chromatography-mass spectrometry after trimethylsilylation. The H
PLC method was also used to measure concentrations of isoflavones and their
glucoside conjugates in various soy-based infant formulas. Total isoflavon
e concentrations varied between 155 and 281 mg/kg. After one woman received
a moderate challenge with 20 g roasted soybeans (equivalent to 37 mg isofl
avones), we detected mean total isoflavone concentrations of approximate to
2.0 mu mol/L in plasma, 0.2 mu mol/L in breast milk, and 3.0 mu mol/h in u
rine. According to our measurements, with adjustment for body weight, isofl
avonoid exposure is 4-6 times higher in infants fed soy-based formula than
in adults eating a diet rich in soyfoods (approximate to 30 g/d). Implicati
ons of the presented results for the potential cancer-preventing activity o
f isoflavones by exposing newborn infants to these phytochemicals are discu
ssed.