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dc.contributor.authorWindsor, Madeline S. A.
dc.contributor.authorBusse, Madleen
dc.contributor.authorMorrison, Daniel E.
dc.contributor.authorBaker, Robert W.
dc.contributor.authorHill, Leila R.
dc.contributor.authorRendina, Louis M.
dc.date.accessioned2025-12-11T00:23:16Z
dc.date.available2025-12-11T00:23:16Z
dc.date.issued2021en
dc.identifier.urihttps://hdl.handle.net/2123/34608
dc.description.abstractThe use of a triphenylarsonium vector for tumour cell-targeting leads to a dramatic increase in Gd3+ uptake in human glioblastoma multiforme cells by up to an order of magnitude over the isosteric triarylphosphonium analogue, with significant implications for ‘theranostic’ applications involving delivery of this important lanthanoid metal ion to tumour cells.en
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.relation.ispartofChemical Communicationsen
dc.rightsCopyright All Rights Reserveden
dc.subjectgadoliniumen
dc.subjectarsoniumen
dc.subjectmitochondriaen
dc.subjecttheranosticen
dc.titleSelective delivery of remarkably high levels of gadolinium to tumour cells using an arsonium salten
dc.typeArticleen
dc.subject.asrcANZSRC FoR code::34 CHEMICAL SCIENCES::3402 Inorganic chemistry::340201 Bioinorganic chemistryen
dc.identifier.doi10.1039/D1CC03082E
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcDP190103461
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.citation.volume57en
usyd.citation.spage8806en
usyd.citation.epage8809en
workflow.metadata.onlyNoen


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