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Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron
(44)Sc has favorable properties for cancer diagnosis using Positron Emission Tomography (PET) making it a promising candidate for application in nuclear medicine. The implementation of its production with existing compact medical cyclotrons would mean the next essential milestone in the development...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587374/ https://www.ncbi.nlm.nih.gov/pubmed/33066650 http://dx.doi.org/10.3390/molecules25204706 |
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author | van der Meulen, Nicholas P. Hasler, Roger Talip, Zeynep Grundler, Pascal V. Favaretto, Chiara Umbricht, Christoph A. Müller, Cristina Dellepiane, Gaia Carzaniga, Tommaso S. Braccini, Saverio |
author_facet | van der Meulen, Nicholas P. Hasler, Roger Talip, Zeynep Grundler, Pascal V. Favaretto, Chiara Umbricht, Christoph A. Müller, Cristina Dellepiane, Gaia Carzaniga, Tommaso S. Braccini, Saverio |
author_sort | van der Meulen, Nicholas P. |
collection | PubMed |
description | (44)Sc has favorable properties for cancer diagnosis using Positron Emission Tomography (PET) making it a promising candidate for application in nuclear medicine. The implementation of its production with existing compact medical cyclotrons would mean the next essential milestone in the development of this radionuclide. While the production and application of (44)Sc has been comprehensively investigated, the development of specific targetry and irradiation methods is of paramount importance. As a result, the target was optimized for the (44)Ca(p,n)(44)Sc nuclear reaction using CaO instead of CaCO(3), ensuring decrease in target radioactive degassing during irradiation and increased radionuclidic yield. Irradiations were performed at the research cyclotron at the Paul Scherrer Institute (~11 MeV, 50 µA, 90 min) and the medical cyclotron at the University of Bern (~13 MeV, 10 µA, 240 min), with yields varying from 200 MBq to 16 GBq. The development of targetry, chemical separation as well as the practical issues and implications of irradiations, are analyzed and discussed. As a proof-of-concept study, the (44)Sc produced at the medical cyclotron was used for a preclinical study using a previously developed albumin-binding prostate-specific membrane antigen (PSMA) ligand. This work demonstrates the feasibility to produce (44)Sc with high yields and radionuclidic purity using a medical cyclotron, equipped with a commercial solid target station. |
format | Online Article Text |
id | pubmed-7587374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75873742020-10-29 Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron van der Meulen, Nicholas P. Hasler, Roger Talip, Zeynep Grundler, Pascal V. Favaretto, Chiara Umbricht, Christoph A. Müller, Cristina Dellepiane, Gaia Carzaniga, Tommaso S. Braccini, Saverio Molecules Article (44)Sc has favorable properties for cancer diagnosis using Positron Emission Tomography (PET) making it a promising candidate for application in nuclear medicine. The implementation of its production with existing compact medical cyclotrons would mean the next essential milestone in the development of this radionuclide. While the production and application of (44)Sc has been comprehensively investigated, the development of specific targetry and irradiation methods is of paramount importance. As a result, the target was optimized for the (44)Ca(p,n)(44)Sc nuclear reaction using CaO instead of CaCO(3), ensuring decrease in target radioactive degassing during irradiation and increased radionuclidic yield. Irradiations were performed at the research cyclotron at the Paul Scherrer Institute (~11 MeV, 50 µA, 90 min) and the medical cyclotron at the University of Bern (~13 MeV, 10 µA, 240 min), with yields varying from 200 MBq to 16 GBq. The development of targetry, chemical separation as well as the practical issues and implications of irradiations, are analyzed and discussed. As a proof-of-concept study, the (44)Sc produced at the medical cyclotron was used for a preclinical study using a previously developed albumin-binding prostate-specific membrane antigen (PSMA) ligand. This work demonstrates the feasibility to produce (44)Sc with high yields and radionuclidic purity using a medical cyclotron, equipped with a commercial solid target station. MDPI 2020-10-14 /pmc/articles/PMC7587374/ /pubmed/33066650 http://dx.doi.org/10.3390/molecules25204706 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article van der Meulen, Nicholas P. Hasler, Roger Talip, Zeynep Grundler, Pascal V. Favaretto, Chiara Umbricht, Christoph A. Müller, Cristina Dellepiane, Gaia Carzaniga, Tommaso S. Braccini, Saverio Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron |
title | Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron |
title_full | Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron |
title_fullStr | Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron |
title_full_unstemmed | Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron |
title_short | Developments toward the Implementation of (44)Sc Production at a Medical Cyclotron |
title_sort | developments toward the implementation of (44)sc production at a medical cyclotron |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587374/ https://www.ncbi.nlm.nih.gov/pubmed/33066650 http://dx.doi.org/10.3390/molecules25204706 |
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