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dc.contributor.authorHall, Andrew J.
dc.contributor.authorRobertson, Amy G.
dc.contributor.authorHill, Leila R.
dc.contributor.authorRendina, Louis M.
dc.date.accessioned2021-03-30T05:03:35Z
dc.date.available2021-03-30T05:03:35Z
dc.date.issued2021en
dc.identifier.urihttps://hdl.handle.net/2123/24767
dc.description.abstractThe synthesis of a new series of Gd(III)-arylphosphonium complexes is described and the solution stability of selected compounds is reported. Their lipophilicity and uptake in human glial (SVG p12) and human glioblastoma multiforme (T98G) cell lines are presented. The in vitro cytotoxicity of all complexes was determined to be low at therapeutically-relevant concentrations. Selected Gd(III) complexes are potential candidates for further investigation as theranostic agents.en
dc.language.isoenen
dc.publisherNatureen
dc.relation.ispartofScientifc Reportsen
dc.rightsCopyright All Rights Reserveden
dc.subjectgadoliniumen
dc.subjectcell uptakeen
dc.subjectdelocalised lipophilic cationen
dc.subjectmitochondriaen
dc.subjectneutron capture therapyen
dc.subjectphoton activation therapyen
dc.subjectDOTAen
dc.titleSynthesis and tumour cell uptake studies of gadolinium(III)–phosphonium complexesen
dc.typeArticleen
dc.subject.asrc03 Chemical Sciencesen
dc.subject.asrc0302 Inorganic Chemistryen
dc.subject.asrc0304 Medicinal and Biomolecular Chemistryen
dc.identifier.doi10.1038/s41598-020-79893-9
dc.relation.arcDP190103461
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.facultySydney Nanoen
usyd.citation.volume11en
usyd.citation.issue1en
usyd.citation.spage598en
workflow.metadata.onlyNoen


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