A simplified GMP-compliant cassette synthesis for ruthenium-mediated 18F-deoxyfluorination of [18F]FPATPP from a phenolic precursor

dc.contributor.authorRajala, Noora A.
dc.contributor.authorKerminen, Edla K.
dc.contributor.authorSalo, Simo A.
dc.contributor.authorVäkiparta, Melina J. J.
dc.contributor.authorKirjavainen, Anna K.
dc.contributor.organizationfi=PET-keskus|en=Turku PET Centre|
dc.contributor.organizationfi=kemian laitos|en=Department of Chemistry|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.14646305228
dc.contributor.organization-code1.2.246.10.2458963.20.27622076134
dc.converis.publication-id491589807
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/491589807
dc.date.accessioned2025-08-27T21:31:37Z
dc.date.available2025-08-27T21:31:37Z
dc.description.abstract<p>Ruthenium-mediated <sup>18</sup>F-deoxyfluorination of phenols is a fairly new, but highly underutilized, labeling method option of tracers for positron emission tomography (PET). Most of the published methods are directed toward peptide syntheses and include extensive preparation steps. This study aimed to simplify ruthenium-mediated <sup>18</sup>Fdeoxyfluorination of [<sup>18</sup>F]FPATPP by using the TRASIS AllinOne synthesis platform. This protocol takes minimal preparation time (1 h) and applies a straightforward synthesis that can be used to produce tracers from their electron-rich phenolic precursors bearing protic functional groups such as alcohols and amines. The new simplified cassette method afforded a novel cannabinoid receptor 1 specific tracer [<sup>18</sup>F]FPATPP with a radiochemical yield of 34 ± 2 %, radiochemical purity of >= 97 %, and a molar activity of 620 ± 75 GBq/µmol. The total synthesis time was 55 min. In addition, we developed an attachable accessory compatible with TRASIS AllinOne to enable needle movement to enhance the synthesis yield. Our results broaden the possibilities of a cassette based synthesis development for <sup>18</sup>F-labeled molecules and bridge the gap between research and GMP compatible synthesis methods.<br></p>
dc.identifier.eissn1873-3328
dc.identifier.jour-issn0022-1139
dc.identifier.olddbid200554
dc.identifier.oldhandle10024/183581
dc.identifier.urihttps://www.utupub.fi/handle/11111/45594
dc.identifier.urnURN:NBN:fi-fe2025082789149
dc.language.isoen
dc.okm.affiliatedauthorRajala, Noora
dc.okm.affiliatedauthorKerminen, Edla
dc.okm.affiliatedauthorSalo, Simo
dc.okm.affiliatedauthorVäkiparta, Melina
dc.okm.affiliatedauthorKirjavainen, Anna
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.publisher.placeLAUSANNE
dc.relation.articlenumber110423
dc.relation.doi10.1016/j.jfluchem.2025.110423
dc.relation.ispartofjournalJournal of Fluorine Chemistry
dc.relation.volume283-284
dc.source.identifierhttps://www.utupub.fi/handle/10024/183581
dc.titleA simplified GMP-compliant cassette synthesis for ruthenium-mediated 18F-deoxyfluorination of [18F]FPATPP from a phenolic precursor
dc.year.issued2025

Tiedostot

Näytetään 1 - 1 / 1
Ladataan...
Name:
1-s2.0-S0022113925000351-main.pdf
Size:
2.11 MB
Format:
Adobe Portable Document Format