DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorDai, L-
dc.creatorZhang, J-
dc.creatorWong, CT-
dc.creatorChan, WTK-
dc.creatorLing, X-
dc.creatorAnderson, CJ-
dc.creatorLaw, GL-
dc.date.accessioned2021-05-13T08:31:32Z-
dc.date.available2021-05-13T08:31:32Z-
dc.identifier.issn0020-1669-
dc.identifier.urihttp://hdl.handle.net/10397/89822-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.titleDesign of functional chiral cyclen-based radiometal chelators for theranosticsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1021/acs.inorgchem.0c03734-
dcterms.abstractA series of water-soluble chiral cyclen-based chelators with chemical handles for selective targeting have been synthesized (cyclen = 1,4,7,10-Tetraazacyclododecane). Optical studies, relaxivity measurements, and competitive titrations were performed to show the versatility of these chiral chelators. The complexations of L3, L4, and L5 with Lu3+, Y3+, Sc3+, and Cu2+ were successfully demonstrated in around 90% to 100% yields. Efficient and rapid radiolabeling of L5 with 177Lu was achieved under mild conditions with 96% yield. The chelators exhibit near quantitative labeling efficiencies with a wide range of radiometal ions, which are promising for the development of targeting specific radiopharmaceutical and molecular magnetic resonance imaging contrast agents.-
dcterms.accessRightsembargoed access-
dcterms.bibliographicCitationInorganic chemistry, 2021, https://doi.org/10.1021/acs.inorgchem.0c03734-
dcterms.isPartOfInorganic chemistry-
dcterms.issued2021-
dc.identifier.scopus2-s2.0-85103460403-
dc.description.validate202105 bchy-
dc.description.oaNot applicable-
dc.identifier.FolderNumbera0741-n01-
dc.identifier.SubFormID1422-
dc.description.fundingSourceRGC-
dc.description.fundingTextPolyU153009/19P, PolyU153013/17P-
dc.description.pubStatusEarly release-
dc.date.embargo0000-00-00 (to be updated)en_US
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