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Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement

Despite the notable health benefits of carotenoids for human health, the majority of human diets worldwide are repeatedly shown to be inadequate in intake of carotenoid‐rich fruits and vegetables, according to current health recommendations. To address this deficit, strategies designed to increase d...

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Detalles Bibliográficos
Autores principales: Salter‐Venzon, Dawna, Kazlova, Valentina, Izzy Ford, Samantha, Intra, Janjira, Klosner, Allison E., Gellenbeck, Kevin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448391/
https://www.ncbi.nlm.nih.gov/pubmed/28572926
http://dx.doi.org/10.1002/fsn3.409
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author Salter‐Venzon, Dawna
Kazlova, Valentina
Izzy Ford, Samantha
Intra, Janjira
Klosner, Allison E.
Gellenbeck, Kevin W.
author_facet Salter‐Venzon, Dawna
Kazlova, Valentina
Izzy Ford, Samantha
Intra, Janjira
Klosner, Allison E.
Gellenbeck, Kevin W.
author_sort Salter‐Venzon, Dawna
collection PubMed
description Despite the notable health benefits of carotenoids for human health, the majority of human diets worldwide are repeatedly shown to be inadequate in intake of carotenoid‐rich fruits and vegetables, according to current health recommendations. To address this deficit, strategies designed to increase dietary intakes and subsequent plasma levels of carotenoids are warranted. When mixed carotenoids are delivered into the intestinal tract simultaneously, competition occurs for micelle formation and absorption, affecting carotenoid bioavailability. Previously, we tested the in vitro viability of a carotenoid mix designed to deliver individual carotenoids sequentially spaced from one another over the 6 hr transit time of the human upper gastrointestinal system. We hypothesized that temporally and spatially separating the individual carotenoids would reduce competition for micelle formation, improve uptake, and maximize efficacy. Here, we test this hypothesis in a double‐blind, repeated‐measure, cross‐over human study with 12 subjects by comparing the change of plasma carotenoid levels for 8 hr after oral doses of a sequentially spaced carotenoid mix, to a matched mix without sequential spacing. We find the carotenoid change from baseline, measured as area under the curve, is increased following consumption of the sequentially spaced mix compared to concomitant carotenoids delivery. These results demonstrate reduced interaction and regulation between the sequentially spaced carotenoids, suggesting improved bioavailability from a novel sequentially spaced carotenoid mix.
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spelling pubmed-54483912017-06-01 Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement Salter‐Venzon, Dawna Kazlova, Valentina Izzy Ford, Samantha Intra, Janjira Klosner, Allison E. Gellenbeck, Kevin W. Food Sci Nutr Original Research Despite the notable health benefits of carotenoids for human health, the majority of human diets worldwide are repeatedly shown to be inadequate in intake of carotenoid‐rich fruits and vegetables, according to current health recommendations. To address this deficit, strategies designed to increase dietary intakes and subsequent plasma levels of carotenoids are warranted. When mixed carotenoids are delivered into the intestinal tract simultaneously, competition occurs for micelle formation and absorption, affecting carotenoid bioavailability. Previously, we tested the in vitro viability of a carotenoid mix designed to deliver individual carotenoids sequentially spaced from one another over the 6 hr transit time of the human upper gastrointestinal system. We hypothesized that temporally and spatially separating the individual carotenoids would reduce competition for micelle formation, improve uptake, and maximize efficacy. Here, we test this hypothesis in a double‐blind, repeated‐measure, cross‐over human study with 12 subjects by comparing the change of plasma carotenoid levels for 8 hr after oral doses of a sequentially spaced carotenoid mix, to a matched mix without sequential spacing. We find the carotenoid change from baseline, measured as area under the curve, is increased following consumption of the sequentially spaced mix compared to concomitant carotenoids delivery. These results demonstrate reduced interaction and regulation between the sequentially spaced carotenoids, suggesting improved bioavailability from a novel sequentially spaced carotenoid mix. John Wiley and Sons Inc. 2016-07-28 /pmc/articles/PMC5448391/ /pubmed/28572926 http://dx.doi.org/10.1002/fsn3.409 Text en © 2016 The Authors. Food Science & Nutrition published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Salter‐Venzon, Dawna
Kazlova, Valentina
Izzy Ford, Samantha
Intra, Janjira
Klosner, Allison E.
Gellenbeck, Kevin W.
Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
title Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
title_full Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
title_fullStr Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
title_full_unstemmed Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
title_short Evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
title_sort evidence for decreased interaction and improved carotenoid bioavailability by sequential delivery of a supplement
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448391/
https://www.ncbi.nlm.nih.gov/pubmed/28572926
http://dx.doi.org/10.1002/fsn3.409
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