2002
DOI: 10.1093/ajcn/76.5.1126
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Safety and pharmacokinetics of purified soy isoflavones: single-dose administration to postmenopausal women,,

Abstract: A single-dose administration of purified unconjugated isoflavones at amounts that exceed normal dietary intakes had minimal clinical toxicity in healthy postmenopausal women. The pharmacokinetic data suggest that chronic dosing at 12-24-h intervals would not lead to progressive accumulation of these isoflavones.

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Cited by 163 publications
(144 citation statements)
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“…In human feeding studies, consumption of high-soy diets for 10 weeks yielded plasma levels of genistein of 700 nM with large interindividual variation [Wiseman et al, 2004]. Dietary supplementation with a purified genistein-daidzein-glycitein ''bullet'' that delivers genistein amounts 3-to 4-fold greater than a soy-rich Japanese diets yielded plasma genistein levels in humans up to 27 lM, with minimal reported DNA toxicity [Bloedon et al, 2002;Miltyk et al, 2003]. In our recent review of the potential genotoxic effects of genistein we note that DNA damaging and other potentially adverse effects were primarily induced by high genistein concentrations in the 25-200 lM dose range, therefore we have used a low 3.125 lM concentration of genistein that we show here to be nontoxic to MCF-7 and MDA-MB-468 breast cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…In human feeding studies, consumption of high-soy diets for 10 weeks yielded plasma levels of genistein of 700 nM with large interindividual variation [Wiseman et al, 2004]. Dietary supplementation with a purified genistein-daidzein-glycitein ''bullet'' that delivers genistein amounts 3-to 4-fold greater than a soy-rich Japanese diets yielded plasma genistein levels in humans up to 27 lM, with minimal reported DNA toxicity [Bloedon et al, 2002;Miltyk et al, 2003]. In our recent review of the potential genotoxic effects of genistein we note that DNA damaging and other potentially adverse effects were primarily induced by high genistein concentrations in the 25-200 lM dose range, therefore we have used a low 3.125 lM concentration of genistein that we show here to be nontoxic to MCF-7 and MDA-MB-468 breast cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…A significant, but not insurmountable, issue is that the oral bioavailabilities of genistein and genistin are modest, with in vivo plasma concentrations of genistein Ϸ0.1-8 M at a dose of 16 mg͞kg of body weight (12,13,57). Liu and Hu's (58) study using Caco-2 cells and perfused rat intestinal models shows that genistein is efficiently absorbed into the intestine, but extensive first-pass metabolism results in formation of 7-OH-glucuronic acid as the major metabolite.…”
Section: Discussionmentioning
confidence: 99%
“…The half-life of genistein in plasma was determined to be 3.2 h for men and 3.8 h for women. These appealing pharmacokinetics suggest that a slow-release formula could be useful (12,13).…”
Section: Discussionmentioning
confidence: 99%
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