Cooperative binding and stabilization of the medicinal pigment curcumin by diamide linked γ-cyclodextrin dimers: a spectroscopic characterization

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dc.contributor.authorHarada, Takaaki
dc.contributor.authorPham, Duc-Truc
dc.contributor.authorLeung, Mandy HM
dc.contributor.authorNgo, Huy Tien
dc.contributor.authorLincoln, Stephen F
dc.contributor.authorEaston, Christopher
dc.contributor.authorKee, Tak W
dc.date.accessioned2015-12-10T22:43:34Z
dc.date.issued2011
dc.date.updated2016-02-24T10:24:01Z
dc.description.abstractDiamide linked γ-cyclodextrin (γ-CD) dimers are used to capture curcumin and suppress its decomposition in water. In this study, succinamide and urea linked γ-CD dimers joined through the C6A carbon on each γ-CD are used. The γ-CD dimers, 66γCD2su a
dc.identifier.issn1520-6106
dc.identifier.urihttp://hdl.handle.net/1885/58225
dc.publisherAmerican Chemical Society
dc.sourceJournal of Physical Chemistry B
dc.subjectKeywords: Cooperative binding; Curcumin; Cyclodextrin dimers; Diamides; Fluorescence intensities; Fluorescence quantum yield; High stability; Hydrogen interaction; In-vivo; Spectroscopic characterization; Succinamide; Surfactant micelles; Association reactions; Bio
dc.titleCooperative binding and stabilization of the medicinal pigment curcumin by diamide linked γ-cyclodextrin dimers: a spectroscopic characterization
dc.typeJournal article
local.bibliographicCitation.issue5
local.bibliographicCitation.lastpage1274
local.bibliographicCitation.startpage1268
local.contributor.affiliationHarada, Takaaki, University of Adelaide
local.contributor.affiliationPham, Duc-Truc, University of Adelaide
local.contributor.affiliationLeung, Mandy HM, University of Adelaide
local.contributor.affiliationNgo, Huy Tien, University of Adelaide
local.contributor.affiliationLincoln, Stephen F, University of Adelaide
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationKee, Tak W, University of Adelaide
local.contributor.authoremailu9500570@anu.edu.au
local.contributor.authoruidEaston, Christopher, u9500570
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030302 - Nanochemistry and Supramolecular Chemistry
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB433
local.identifier.citationvolume115
local.identifier.doi10.1021/jp1096025
local.identifier.scopusID2-s2.0-79952846859
local.identifier.thomsonID000286797700058
local.identifier.uidSubmittedByu4005981
local.type.statusPublished Version

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