Membrane-based microfluidic solvent extraction of Ga-68 from aqueous Zn solutions: towards an automated cyclotron production loop.

Cyclotron production Ga-68 Medical radionuclide production Metal contaminants Microfluidic solvent extraction Zinc nitrate liquid target

Journal

EJNMMI radiopharmacy and chemistry
ISSN: 2365-421X
Titre abrégé: EJNMMI Radiopharm Chem
Pays: England
ID NLM: 101714628

Informations de publication

Date de publication:
05 May 2023
Historique:
received: 15 03 2023
accepted: 25 04 2023
medline: 6 5 2023
pubmed: 6 5 2023
entrez: 5 5 2023
Statut: epublish

Résumé

The radionuclide Ga-68 is commonly used in nuclear medicine, specifically in positron emission tomography (PET). Recently, the interest in producing Ga-68 by cyclotron irradiation of [ To eventually allow switching from batch to continuous production, conventional batch extraction and membrane-based microfluidic extraction were compared. In both approaches, Ga-68 was extracted using N-benzoyl-N-phenylhydroxylamine in chloroform as the organic extracting phase. Extraction efficiencies of up to 99.5% ± 0.6% were achieved within 10 min, using the batch approach. Back-extraction of Ga-68 into 2 M HCl was accomplished within 1 min with efficiencies of up to 94.5% ± 0.6%. Membrane-based microfluidic extraction achieved 99.2% ± 0.3% extraction efficiency and 95.8% ± 0.8% back-extraction efficiency into 6 M HCl. When executed on a solution irradiated with a 13 MeV cyclotron at TRIUMF, Canada, comparable efficiencies of 97.0% ± 0.4% were achieved. Zn contamination in the back-extracted Ga-68 solution was found to be below 3 ppm. Microfluidic solvent extraction is a promising method in the production of Ga-68 achieving high efficiencies in a short amount of time, potentially allowing for direct target recycling.

Sections du résumé

BACKGROUND BACKGROUND
The radionuclide Ga-68 is commonly used in nuclear medicine, specifically in positron emission tomography (PET). Recently, the interest in producing Ga-68 by cyclotron irradiation of [
RESULTS RESULTS
To eventually allow switching from batch to continuous production, conventional batch extraction and membrane-based microfluidic extraction were compared. In both approaches, Ga-68 was extracted using N-benzoyl-N-phenylhydroxylamine in chloroform as the organic extracting phase. Extraction efficiencies of up to 99.5% ± 0.6% were achieved within 10 min, using the batch approach. Back-extraction of Ga-68 into 2 M HCl was accomplished within 1 min with efficiencies of up to 94.5% ± 0.6%. Membrane-based microfluidic extraction achieved 99.2% ± 0.3% extraction efficiency and 95.8% ± 0.8% back-extraction efficiency into 6 M HCl. When executed on a solution irradiated with a 13 MeV cyclotron at TRIUMF, Canada, comparable efficiencies of 97.0% ± 0.4% were achieved. Zn contamination in the back-extracted Ga-68 solution was found to be below 3 ppm.
CONCLUSIONS CONCLUSIONS
Microfluidic solvent extraction is a promising method in the production of Ga-68 achieving high efficiencies in a short amount of time, potentially allowing for direct target recycling.

Identifiants

pubmed: 37147500
doi: 10.1186/s41181-023-00195-2
pii: 10.1186/s41181-023-00195-2
pmc: PMC10163183
doi:

Types de publication

Journal Article

Langues

eng

Pagination

9

Subventions

Organisme : Nederlandse Organisatie voor Wetenschappelijk Onderzoek
ID : 16913

Informations de copyright

© 2023. The Author(s).

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Auteurs

Svenja Trapp (S)

Department of Radiation Science and Technology, Reactor Institute Delft, Delft University of Technology, Mekelweg 15, 2629 JB, Delft, The Netherlands.

Tom Lammers (T)

Department of Radiation Science and Technology, Reactor Institute Delft, Delft University of Technology, Mekelweg 15, 2629 JB, Delft, The Netherlands.

Gokce Engudar (G)

Life Sciences Division, TRIUMF, Vancouver, BC, Canada.

Cornelia Hoehr (C)

Life Sciences Division, TRIUMF, Vancouver, BC, Canada.

Antonia G Denkova (AG)

Department of Radiation Science and Technology, Reactor Institute Delft, Delft University of Technology, Mekelweg 15, 2629 JB, Delft, The Netherlands.

Elisabeth Paulssen (E)

Department of Radiation Science and Technology, Reactor Institute Delft, Delft University of Technology, Mekelweg 15, 2629 JB, Delft, The Netherlands.
Department of Chemistry and Biotechnology, Aachen University of Applied Science, Juelich, Germany.

Robin M de Kruijff (RM)

Department of Radiation Science and Technology, Reactor Institute Delft, Delft University of Technology, Mekelweg 15, 2629 JB, Delft, The Netherlands. r.m.dekruijff@tudelft.nl.

Classifications MeSH