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Efficient preparation of high-quality (64)Cu for routine use.
Nuclear Medicine and Biology 2016 November
INTRODUCTION: Copper-64 is an attractive radionuclide for positron emission tomography and is emerging as a radiotherapeutic agent. The demand of (64)Cu with low metallic impurities has increased because of its wide applications when incorporated with antibodies, peptides, and proteins. In this study, we propose a new separation method to produce high-quality (64)Cu using a cation exchange column, as well as an automated separation system suitable for large-scale production.
METHODS: (64)Cu was produced from an electrodeposited (64)Ni target via the (64)Ni(p,n)-reaction with a 24MeV HH+ beam at 10eμA (electrical microampere) conducted for 1-3h. The irradiated target was transported to a hot cell and disassembled remotely. (64)Cu was separated by a solvent mixture of HCl and acetone on a cation-exchange resin, AG50W-X8. The chemical purity of (64)Cu final product was evaluated using ion-chromatography coupled with a UV detector and inductively coupled plasma mass spectroscopy for quality as well as metallic impurities.
RESULTS: We obtained (64)Cu in dried form at a yield of 5.2-13GBq at the end of separation, or 521±12MBq/eμAh as the final product within 2.5h of processing time. The metallic impurities were a satisfactory low level in the order of ppb. Major contaminants of Co and Ni were lower than those samples obtained by a widely accepted separation using an anion-exchange resin.
CONCLUSION: Using a cation-exchange resin and a systematic operation, we successfully reduced the contamination level of the (64)Cu product. As a straightforward separation method, which shortened the entire processing time, we obtained a satisfactory amount of high-quality (64)Cu available for routine use.
METHODS: (64)Cu was produced from an electrodeposited (64)Ni target via the (64)Ni(p,n)-reaction with a 24MeV HH+ beam at 10eμA (electrical microampere) conducted for 1-3h. The irradiated target was transported to a hot cell and disassembled remotely. (64)Cu was separated by a solvent mixture of HCl and acetone on a cation-exchange resin, AG50W-X8. The chemical purity of (64)Cu final product was evaluated using ion-chromatography coupled with a UV detector and inductively coupled plasma mass spectroscopy for quality as well as metallic impurities.
RESULTS: We obtained (64)Cu in dried form at a yield of 5.2-13GBq at the end of separation, or 521±12MBq/eμAh as the final product within 2.5h of processing time. The metallic impurities were a satisfactory low level in the order of ppb. Major contaminants of Co and Ni were lower than those samples obtained by a widely accepted separation using an anion-exchange resin.
CONCLUSION: Using a cation-exchange resin and a systematic operation, we successfully reduced the contamination level of the (64)Cu product. As a straightforward separation method, which shortened the entire processing time, we obtained a satisfactory amount of high-quality (64)Cu available for routine use.
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