Evidence map›Paper›PMID 41364300›Full record

ArticleEJNMMI radiopharmacy and chemistry2025

Aluminum-[

Anisa Biti, Surachet Imlimthan, Heidi Harjunpää, Diana Barakhtii, Topias Pöllänen, Arina Sukhova, Susanne K Wiedmer, Filip S Ekholm, Susanna Fagerholm, Mirkka Sarparanta

Abstract read
In one paragraph

Article in EJNMMI radiopharmacy and chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Anisa BitiDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Surachet ImlimthanDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Heidi HarjunpääMolecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Viikinkaari 9, 00790, Helsinki, Finland.
Diana BarakhtiiDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Topias PöllänenDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Arina SukhovaDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Susanne K WiedmerDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Filip S EkholmDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland.
Susanna FagerholmMolecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Viikinkaari 9, 00790, Helsinki, Finland.
Mirkka SarparantaDepartment of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, 00560, Helsinki, Finland. mirkka.sarparanta@helsinki.fi.ORCID http://orcid.org/0000-0002-2956-4366

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of safer and more effective cell-based therapies requires robust methods for tracking cells in vivo. Positron emission tomography (PET) is a highly sensitive nuclear imaging technique capable of quantitatively tracking the in vivo fate of cells after administration. Here, we investigated a cell-labeling strategy based on metabolic glycoengineering (MGE) to introduce azides on the cell surface, followed by radiolabeling via the bioorthogonal perfluoroaryl azide (PFAA)-Staudinger reaction. We studied the metabolic incorporation of a tetraacetylated PFAA-derivatized mannosamine in Jurkat cells and evaluated whether three triarylphosphines bearing the REstrained Complexing Agent (RESCA), could be radiolabeled with aluminum-[F]fluoride (Al[

resultsThree novel triarylphosphines containing different linkers (hydrophilic ester, ethylenediamine, and cyclohexyl) between the phosphine moiety and the (+)-RESCA-chelator were synthesized and characterized. Kinetic assays showed that all compounds reacted with the PFAA-derivatized monosaccharide, exhibiting different reaction kinetics under the tested conditions. They were successfully radiolabeled with fluorine-18 under optimized mild conditions and provided key insights into the radiolabeling of small molecules bearing the RESCA-chelator. The ester derivative underwent rapid chemical decomposition while the ethylenediamine- and cyclohexyl-linked derivatives were more resistant, with the cyclohexyl analogue showing the highest stability against demetallation and/or defluorination. However, radiolabeling with Al[

conclusionsWhile the Al[

Indexed as

Aluminum-[18F]fluorideBioorthogonal chemistryFluorine-18In vivo cell trackingMetabolic glycoengineering (MGE)Perfluoroaryl azide (PFAA)Positron emission tomography (PET)Staudinger ligation

Identifiers

PMID41364300
PMCPMC12705485

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.