Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/1787
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorBenzie, IFF-
dc.creatorChung, WY-
dc.creatorWang, J-
dc.creatorRichelle, M-
dc.creatorBucheli, P-
dc.date.accessioned2014-12-11T08:25:12Z-
dc.date.available2014-12-11T08:25:12Z-
dc.identifier.issn0007-1145-
dc.identifier.urihttp://hdl.handle.net/10397/1787-
dc.language.isoenen_US
dc.publisherCambridge University Pressen_US
dc.rights© The Authors 2006.en_US
dc.rightsThe journal web page is located at: http://journals.cambridge.org/action/displayJournal?jid=BJNen_US
dc.subjectWolfberryen_US
dc.subjectKei Tzeen_US
dc.subjectGou Qi Zien_US
dc.subjectChinese medicineen_US
dc.subjectMacular degenerationen_US
dc.subjectZeaxanthinen_US
dc.titleEnhanced bioavailability of zeaxanthin in a milk-based formulation of wolfberry (Gou Qi Zi; Fructus barbarum L.)en_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationAuthor name used in this publication: Wai Y. Chungen_US
dc.identifier.spage154-
dc.identifier.epage160-
dc.identifier.volume96-
dc.identifier.issue1-
dc.identifier.doi10.1079/BJN20061796-
dcterms.abstractThe carotenoid zeaxanthin is concentrated within the macula. Increased macular zeaxanthin is suggested to lower the risk of age-related macular degeneration. The small red berry, wolfberry (Fructus barbarum L.; Gou Qi Zi and Kei Tze), is one of the richest natural sources of zeaxanthin. However, carotenoid bioavailability is low, and food-based products with enhanced bioavailability are of interest. The present study investigated zeaxanthin bioavailability from three wolfberry formulations. Berries were homogenised in hot (80°C) water, warm (40°C) skimmed milk and hot (80°C) skimmed milk, with freeze drying of each preparation into a powdered form. A zeaxanthin-standardised dose (15mg) of each was consumed, in randomised order, together with a standardised breakfast by twelve healthy, consenting subjects in a cross-over trial, with a 3–5-week washout period between treatments. Blood samples were taken via a venous cannula immediately before (fasting) and 2, 4, 6, 7, 8 and 10h post-ingestion. Zeaxanthin concentration in the triacylglycerol-rich lipoprotein fraction of plasma was measured by HPLC. Results showed that triacylglycerol-rich lipoprotein zeaxanthin peaked at 6h post-ingestion for all formulations. Zeaxanthin bioavailability from the hot milk formulation was significantly higher (p<0·001) than from the others. Mean area under the curve (n 12) results were 9·73 (sem 2·45), 3·24 (sem 0·72) and 3·14 (sem 1·09) nmol×h/l for the hot milk, warm milk and hot water formulations, respectively. Results showed clearly that homogenisation of wolfberry in hot skimmed milk results in a formulation that has a 3-fold enhanced bioavailability of zeaxanthin compared with both the ‘classical’ hot water and warm skimmed milk treatment of the berries.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBritish journal of nutrition, Jan. 2006, v. 96, no. 1, p. 154-160-
dcterms.isPartOfBritish journal of nutrition-
dcterms.issued2006-01-
dc.identifier.isiWOS:000239283600022-
dc.identifier.scopus2-s2.0-33746774657-
dc.identifier.pmid16870004-
dc.identifier.eissn1475-2662-
dc.identifier.rosgroupidr30433-
dc.description.ros2006-2007 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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