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Bioavailability and bioefficacy of polyphenols in humans I Review of 97 bioavailability studies Manach C; Williamson G; Morand C; Scalbert A; Remesy CAm J Clin Nutr 2005[Jan]; 81 (1 Suppl): 230S-242SPolyphenols are abundant micronutrients in our diet, and evidence for their role in the prevention of degenerative diseases is emerging. Bioavailability differs greatly from one polyphenol to another, so that the most abundant polyphenols in our diet are not necessarily those leading to the highest concentrations of active metabolites in target tissues. Mean values for the maximal plasma concentration, the time to reach the maximal plasma concentration, the area under the plasma concentration-time curve, the elimination half-life, and the relative urinary excretion were calculated for 18 major polyphenols. We used data from 97 studies that investigated the kinetics and extent of polyphenol absorption among adults, after ingestion of a single dose of polyphenol provided as pure compound, plant extract, or whole food/beverage. The metabolites present in blood, resulting from digestive and hepatic activity, usually differ from the native compounds. The nature of the known metabolites is described when data are available. The plasma concentrations of total metabolites ranged from 0 to 4 mumol/L with an intake of 50 mg aglycone equivalents, and the relative urinary excretion ranged from 0.3% to 43% of the ingested dose, depending on the polyphenol. Gallic acid and isoflavones are the most well-absorbed polyphenols, followed by catechins, flavanones, and quercetin glucosides, but with different kinetics. The least well-absorbed polyphenols are the proanthocyanidins, the galloylated tea catechins, and the anthocyanins. Data are still too limited for assessment of hydroxycinnamic acids and other polyphenols. These data may be useful for the design and interpretation of intervention studies investigating the health effects of polyphenols.|Adult[MESH]|Anthocyanins/blood/*pharmacokinetics/urine[MESH]|Area Under Curve[MESH]|Biological Availability[MESH]|Female[MESH]|Flavonoids/metabolism/*pharmacokinetics/therapeutic use[MESH]|Food Analysis[MESH]|Half-Life[MESH]|Humans[MESH]|Intestinal Absorption[MESH]|Isoflavones/blood/*pharmacokinetics/urine[MESH]|Male[MESH]|Phenols/metabolism/*pharmacokinetics/therapeutic use[MESH]|Polyphenols[MESH] |
