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Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging 11/2010

01.11.2010 | Original Article

Reduced dimethylaminoethanol in [18F]fluoromethylcholine: an important step towards enhanced tumour visualization

verfasst von: Dominique Slaets, Sylvie De Bruyne, Caroline Dumolyn, Lieselotte Moerman, Koen Mertens, Filip De Vos

Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging | Ausgabe 11/2010

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Abstract

Purpose

[18F]Fluoromethylcholine ([18F]FCho) is a radiotracer generally used for tumour visualization in patients. Due to high levels of dimethylaminoethanol (DMAE) remaining in [18F]FCho solutions synthesized by currently available methods, tumour visualization might be compromised.

Methods

An improved purification method involving an optimized purification step for reducing the levels of DMAE was conceived. The physiological explanation for the interference of residual DMAE in [18F]FCho pharmacokinetics was further elaborated in a xenograft mouse model.

Results

The use of a series of polymer solid-phase extraction cartridges (Oasis HLB/WCX), instead of the commonly used combination of tC18 and Accell CM cartridges, reduced DMAE levels from 402.2±49.6 ppm to 3.0±0.5 ppm. Subsequent in vitro tests proved that (1) [18F]FCho uptake was reduced in the presence of DMAE at concentrations above 0.5 µM and (2) DMAE is a competitive inhibitor of [18F]FCho transport. In vivo experiments in xenograft mouse models corroborated reduced tumour uptake at DMAE plasma levels of about 2.5 µM as found in patients injected with contaminated [18F]FCho.

Conclusion

Residual DMAE, even at levels below choline plasma concentrations found during fasting, compromises [18F]FCho uptake in vivo and care should be taken to avoid its interference in molecular imaging with [18F]FCho.
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Metadaten
Titel
Reduced dimethylaminoethanol in [18F]fluoromethylcholine: an important step towards enhanced tumour visualization
verfasst von
Dominique Slaets
Sylvie De Bruyne
Caroline Dumolyn
Lieselotte Moerman
Koen Mertens
Filip De Vos
Publikationsdatum
01.11.2010
Verlag
Springer-Verlag
Erschienen in
European Journal of Nuclear Medicine and Molecular Imaging / Ausgabe 11/2010
Print ISSN: 1619-7070
Elektronische ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-010-1508-z

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