On-cartridge preparation and evaluation of 68Ga-, 89Zr- and 64Cu-precursors for cell radiolabelling
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31128475
DOI
10.1016/j.nucmedbio.2019.04.001
PII: S0969-8051(19)30009-5
Knihovny.cz E-zdroje
- Klíčová slova
- Cell labelling, Copper-64, Gallium-68, On-cartridge complex formation, PET, Zirconium-89,
- MeSH
- erytrocyty metabolismus MeSH
- izotopové značení MeSH
- leukocyty metabolismus MeSH
- myši MeSH
- PET/CT MeSH
- radiochemie přístrojové vybavení MeSH
- radioizotopy galia chemie metabolismus MeSH
- radioizotopy mědi chemie metabolismus MeSH
- radionuklidy chemie metabolismus MeSH
- zirkonium chemie metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- Copper-64 MeSH Prohlížeč
- Gallium-68 MeSH Prohlížeč
- radioizotopy galia MeSH
- radioizotopy mědi MeSH
- radionuklidy MeSH
- Zirconium-89 MeSH Prohlížeč
- zirkonium MeSH
INTRODUCTION: Indium-111 when formulated as indium-111 oxine remains the gold standard for long term cell tracking, whereas radiometals for improved PET applications still have to be established. We here describe the on-cartridge formation of gallium-68, zirconium-89 and copper-64 complexes in small volumes suitable for cell labelling, including labelling of red blood cells (RBC) and white blood cells (WBC) and their biological evaluation in vivo. METHODS: Small volumes (1-2 mL) of tracers (oxine, tropolone) were directly prepared on an anion exchange cartridge (Sep-Pak QMA). Cells were radiolabelled and the labelling efficiency and efflux were evaluated. The in vivo biodistribution of copper-64-labelled WBC using [64Cu][Cu(oxinate)2] and [64Cu][Cu(tropolonate)2] was monitored in an infection and inflammation animal model using BALB/c mice. RESULTS: On-cartridge concentration of gallium-68, zirconium-89 and copper-64 enabled formation of oxine and tropolone tracers in small volumes with good yields (≥50%) and quality (extraction ≥90%). Prepared tracers radiolabelled the RBC comparable to indium-111 tracers and in vivo biodistribution of copper-64 labelled WBC showed clear accumulation of cells at the site of infection and inflammation. CONCLUSIONS: This on-cartridge preparation method enables simple formation of various PET tracers for cell radiolabelling. Zirconium-89 and copper-64 tracers radiolabelled cells with sufficient stability. Due to their longer half-life this approach could be promising for routine applications where longer evaluation periods for cell tracking are needed. ADVANCES IN KNOWLEDGE AND IMPLICATIONS FOR PATIENT CARE: This novel approach for on-cartridge concentration and preparation of oxine and tropolone precursors with different positron emitters, in small volume and suitable pH, offers a versatile tool towards cell labelling for preclinical and clinical PET applications.
Blood Transfusion Centre of Slovenia Ljubljana Slovenia
Department of Nuclear Medicine Medical University of Innsbruck Innsbruck Austria
Department of Nuclear Medicine University Medical Centre Ljubljana Ljubljana Slovenia
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