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dc.contributor.authorJamieson, Lauren E.
dc.contributor.authorCamus, Victoria L.
dc.contributor.authorBagnaninchi, Pierre O.
dc.contributor.authorFisher, Kate M.
dc.contributor.authorStewart, Grant D.
dc.contributor.authorNailon, William H.
dc.contributor.authorMcLaren, Duncan B.
dc.contributor.authorHarrison, David James
dc.contributor.authorCampbell, Colin J.
dc.date.accessioned2016-09-14T15:30:23Z
dc.date.available2016-09-14T15:30:23Z
dc.date.issued2016-10-07
dc.identifier.citationJamieson , L E , Camus , V L , Bagnaninchi , P O , Fisher , K M , Stewart , G D , Nailon , W H , McLaren , D B , Harrison , D J & Campbell , C J 2016 , ' Targeted SERS nanosensors measure physicochemical gradients and free energy changes in live 3D tumor spheroids ' , Nanoscale , vol. 8 , no. 37 , pp. 16710-16718 . https://doi.org/10.1039/C6NR06031Een
dc.identifier.issn2040-3364
dc.identifier.otherPURE: 245601332
dc.identifier.otherPURE UUID: db1fc12e-d696-4cde-9aa1-467e5c4ca227
dc.identifier.otherScopus: 84988732016
dc.identifier.otherWOS: 000387857700016
dc.identifier.otherORCID: /0000-0001-9041-9988/work/64034353
dc.identifier.urihttps://hdl.handle.net/10023/9500
dc.descriptionCJC is grateful to the Leverhulme trust for support (Project Grant RPG-2012-680). VLC is grateful to the Jamie King Cancer Research Fund for funding.en
dc.description.abstractUse of multicellular tumor spheroids (MTS) to investigate therapies has gained impetus because they have potential to mimic factors including zonation, hypoxia and drug-resistance. However, analysis remains difficult and often destroys 3D integrity. Here we report an optical technique using targeted nanosensors that allows in situ 3D mapping of redox potential gradients whilst retaining MTS morphology and function. The magnitude of the redox potential gradient can be quantified as a free energy difference (ΔG) and used as a measurement of MTS viability. We found that by delivering different doses of radiotherapy to MTS we could correlate loss of ΔG with increasing therapeutic dose. In addition, we found that resistance to drug therapy was indicated by an increase in ΔG. This robust and reproducible technique allows interrogation of an in vitro tumor-model's bioenergetic response to therapy, indicating its potential as a tool for therapy development.
dc.format.extent9
dc.language.isoeng
dc.relation.ispartofNanoscaleen
dc.rightsCopyright 2016 the Author(s), published by the Royal Society of Chemistry. This Open Access Article is licensed under a Creative Commons Attribution 3.0 Unported Licence.en
dc.subjectNanosensoren
dc.subjectSERSen
dc.subjectSpheroiden
dc.subjectRedoxen
dc.subjectFree-energyen
dc.subjectRC0254 Neoplasms. Tumors. Oncology (including Cancer)en
dc.subjectRM Therapeutics. Pharmacologyen
dc.subjectT Technologyen
dc.subjectNDASen
dc.subjectBDCen
dc.subjectR2Cen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccRC0254en
dc.subject.lccRMen
dc.subject.lccTen
dc.titleTargeted SERS nanosensors measure physicochemical gradients and free energy changes in live 3D tumor spheroidsen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.1039/C6NR06031E
dc.description.statusPeer revieweden


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