Pretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles

dc.contributor.authorKeinanen O
dc.contributor.authorMakila EM
dc.contributor.authorLindgren R
dc.contributor.authorVirtanen H
dc.contributor.authorLiljenback H
dc.contributor.authorOikonen V
dc.contributor.authorSarparanta M
dc.contributor.authorMolthoff C
dc.contributor.authorWindhorst AD
dc.contributor.authorRoivainen A
dc.contributor.authorSalonen JJ
dc.contributor.authorAiraksinen AJ
dc.contributor.organizationfi=kemian laitos|en=Department of Chemistry|
dc.contributor.organization-code1.2.246.10.2458963.20.66904373678
dc.converis.publication-id27226908
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/27226908
dc.date.accessioned2022-10-28T14:23:24Z
dc.date.available2022-10-28T14:23:24Z
dc.description.abstractPretargeted positron emission tomography (PET) imaging based on bioorthogonal chemical reactions has proven its potential in immunoimaging. It may also have great potential in nanotheranostic applications. Here, we report the first successful pretargeted PET imaging of trans-cyclooctene-modified mesoporous silicon nanoparticles, using F-18-labeled tetrazine as a tracer. The inverse electron-demand Diels-Alder cycloaddition (IEDDA) reaction was fast, resulting in high radioactivity accumulation in the expected organs within 10 min after the administration of the tracer. The highest target-to-background ratio was achieved 120 min after the tracer injection. A clear correlation between the efficiency of the in vivo IEDDA labeling reaction and the injected amount of the tracer was observed. The radioactivity accumulation decreased with the increased amount of the co-injected carrier, indicating saturation in the reaction sites. This finding was supported by the in vitro results. Our study suggests that pretargeted imaging has excellent potential in nanotheranostic PET imaging when using high-specific-activity tracers.
dc.format.pagerange69
dc.identifier.eissn2470-1343
dc.identifier.olddbid187983
dc.identifier.oldhandle10024/171077
dc.identifier.urihttps://www.utupub.fi/handle/11111/43453
dc.identifier.urlhttp://pubs.acs.org/doi/abs/10.1021/acsomega.6b00269
dc.identifier.urnURN:NBN:fi-fe2021042717368
dc.language.isoen
dc.okm.affiliatedauthorMäkilä, Ermei
dc.okm.affiliatedauthorLindgren, Rici
dc.okm.affiliatedauthorAiraksinen, Anu
dc.okm.affiliatedauthorVirtanen, Helena
dc.okm.affiliatedauthorLiljenbäck, Heidi
dc.okm.affiliatedauthorOikonen, Vesa
dc.okm.affiliatedauthorRoivainen, Anne
dc.okm.affiliatedauthorSalonen, Jarno
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAMER CHEMICAL SOC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1021/acsomega.6b00269
dc.relation.ispartofjournalACS Omega
dc.relation.issue1
dc.relation.volume2
dc.source.identifierhttps://www.utupub.fi/handle/10024/171077
dc.titlePretargeted PET Imaging of trans-Cyclooctene-Modified Porous Silicon Nanoparticles
dc.year.issued2017

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