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dc.contributor.authorAlhourani, Abdelnour
dc.contributor.authorFørde, Jan-Lukas
dc.contributor.authorEichacker, Lutz Andreas
dc.contributor.authorHerfindal, Lars
dc.contributor.authorHagland, Hanne Røland
dc.date.accessioned2021-11-23T08:50:19Z
dc.date.available2021-11-23T08:50:19Z
dc.date.created2021-10-18T12:27:45Z
dc.date.issued2021
dc.identifier.issn2470-1343
dc.identifier.urihttps://hdl.handle.net/11250/2830895
dc.description.abstractGraphene-based drug carriers provide a promising addition to current cancer drug delivery options. Increased accessibility of high-quality graphene made by plasma-enhanced chemical vapor deposition (PE-CVD) makes it an attractive material to revisit in comparison to the widely studied graphene oxide (GO) in drug delivery. Here, we show the potential of repurposing the metabolic drug phenformin for cancer treatment in terms of stability, binding, and pH-responsive release. Using covalent attachment of poly(ethylene glycol) (PEG) onto pristine (PE-CVD) graphene, we show that PEG stabilized graphene nanosheets (PGNS) are stable in aqueous solutions and exhibit higher binding affinity toward phenformin than GO. Moreover, we experimentally demonstrate an improved drug release from PGNS than GO at pH levels lower than physiological conditions, yet comparable to that found in tumor microenvironments.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.urihttps://pubs.acs.org/doi/abs/10.1021/acsomega.1c03283
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleImproved pH-Responsive Release of Phenformin from Low-Defect Graphene Compared to Graphene Oxideen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 the authorsen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1021/acsomega.1c03283
dc.identifier.cristin1946671
dc.source.journalACS Omegaen_US
dc.source.pagenumber24619-24629en_US
dc.identifier.citationACS Omega. 2021, 6 (38), 24619-24629.en_US
dc.source.volume6en_US
dc.source.issue38en_US


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