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Recoveries in ileal fluid indicated that 67% of hydroxycinnamate tartarate esters, and smaller percentages of the intake of other (poly)phenolic compounds, pass from the small intestine to the colon. The juice was also ingested by healthy subjects with an intact functioning colon. Peak plasma concentrations (<jats:italic>C<\/jats:italic><jats:sub>max<\/jats:sub>) ranged from 1.0 nmol\/L for petunidin\u20103\u2010<jats:italic>O<\/jats:italic>\u2010glucoside to 355 nmol\/L for dihydrocoumaric acid. Urinary excretion, as an indicator of bioavailability, varied from 0.26% for total anthocyanins to 24% for metabolites of hydroxycinnamate tartarate esters. The <jats:italic>C<\/jats:italic><jats:sub>max<\/jats:sub> times of the anthocyanins indicated that their low level absorption occurred in the small intestine in contrast to hydroxycinnamate metabolites which were absorbed in both the small and the large intestine where the colonic microflora appeared responsible for hydrogenation of the hydroxycinnamate side chain. The bioavailability of the complex mixture of (poly)phenolic compounds in Concord grape juice, was very similar to that observed in previous studies when compounds were either fed individually or as major components in products containing a restricted spectrum of (poly)phenolic compounds.<\/jats:p>","DOI":"10.1002\/mnfr.201100566","type":"journal-article","created":{"date-parts":[[2012,2,14]],"date-time":"2012-02-14T07:52:31Z","timestamp":1329205951000},"page":"497-509","source":"Crossref","is-referenced-by-count":117,"title":["Gastrointestinal stability and bioavailability of (poly)phenolic compounds following ingestion of Concord grape juice by humans"],"prefix":"10.1002","volume":"56","author":[{"given":"Angelique","family":"Stalmach","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christine A.","family":"Edwards","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"JoLynne D.","family":"Wightman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alan","family":"Crozier","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2012,2,14]]},"reference":[{"key":"e_1_2_1_2_2","doi-asserted-by":"publisher","DOI":"10.1021\/jf2015039"},{"key":"e_1_2_1_3_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ijdevneu.2005.06.001"},{"key":"e_1_2_1_4_2","doi-asserted-by":"publisher","DOI":"10.1093\/ajcn\/84.1.252"},{"key":"e_1_2_1_5_2","doi-asserted-by":"publisher","DOI":"10.1158\/0008-5472.CAN-06-4069"},{"key":"e_1_2_1_6_2","doi-asserted-by":"publisher","DOI":"10.1017\/S0007114509992364"},{"key":"e_1_2_1_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.atherosclerosis.2006.03.017"},{"key":"e_1_2_1_8_2","doi-asserted-by":"publisher","DOI":"10.1021\/jf030278l"},{"key":"e_1_2_1_9_2","first-page":"1466","article-title":"Resveratrol causes WAF\u20101\/p21\u2010mediated G(1)\u2010phase arrest of cell cycle and induction of apoptosis in human epidermoid carcinoma A431 cells","volume":"7","author":"Ahmad N.","year":"2001","journal-title":"Clin. 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