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Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies
BACKGROUND: (S)-4-(3-(18)F-Fluoropropyl)-L-Glutamic Acid ([(18)F]FSPG) is a positron emission tomography (PET) tracer that specifically targets the cystine/glutamate antiporter (xc(−)), which is frequently overexpressed in cancer and several neurological disorders. Pilot studies examining the dosime...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366059/ https://www.ncbi.nlm.nih.gov/pubmed/37486582 http://dx.doi.org/10.1186/s41181-023-00200-8 |
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author | Lin, Mai Ta, Robert T. Manning, H. Charles |
author_facet | Lin, Mai Ta, Robert T. Manning, H. Charles |
author_sort | Lin, Mai |
collection | PubMed |
description | BACKGROUND: (S)-4-(3-(18)F-Fluoropropyl)-L-Glutamic Acid ([(18)F]FSPG) is a positron emission tomography (PET) tracer that specifically targets the cystine/glutamate antiporter (xc(−)), which is frequently overexpressed in cancer and several neurological disorders. Pilot studies examining the dosimetry and biodistribution of [(18)F]FSPG in healthy volunteers and tumor detection in patients with non-small cell lung cancer, hepatocellular carcinoma, and brain tumors showed promising results. In particular, low background uptake in the brain, lung, liver, and bowel was observed that further leads to excellent imaging contrasts of [(18)F]FSPG PET. However, reliable production-scale cGMP-compliant automated procedures for [(18)F]FSPG production are still lacking to further increase the utility and clinical adoption of this radiotracer. Herein, we report the optimized automated approaches to produce [(18)F]FSPG through two commercially available radiosynthesizers capable of supporting centralized and large-scale production for clinical use. RESULTS: Starting with activity levels of 60–85 GBq, the fully-automated process to produce [(18)F]FSPG took less than 45 min with average radiochemical yields of 22.56 ± 0.97% and 30.82 ± 1.60% (non-decay corrected) using TRACERlab™ FXFN and FASTlab™, respectively. The radiochemical purities were > 95% and the formulated [(18)F]FSPG solution was determined to be sterile and colorless with the pH of 6.5–7.5. No radiolysis of the product was observed up to 8 h after final batch formulation. CONCLUSIONS: In summary, cGMP-compliant radiosyntheses and quality control of [(18)F]FSPG have been established on two commercially available synthesizers leveraging high activity concentration and radiochemical purity. While the clinical trials using [(18)F]FSPG PET are currently underway, the automated approaches reported herein will accelerate the clinical adoption of this radiotracer and warrant centralized and large-scale production of [(18)F]FSPG. |
format | Online Article Text |
id | pubmed-10366059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-103660592023-07-26 Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies Lin, Mai Ta, Robert T. Manning, H. Charles EJNMMI Radiopharm Chem Methodology BACKGROUND: (S)-4-(3-(18)F-Fluoropropyl)-L-Glutamic Acid ([(18)F]FSPG) is a positron emission tomography (PET) tracer that specifically targets the cystine/glutamate antiporter (xc(−)), which is frequently overexpressed in cancer and several neurological disorders. Pilot studies examining the dosimetry and biodistribution of [(18)F]FSPG in healthy volunteers and tumor detection in patients with non-small cell lung cancer, hepatocellular carcinoma, and brain tumors showed promising results. In particular, low background uptake in the brain, lung, liver, and bowel was observed that further leads to excellent imaging contrasts of [(18)F]FSPG PET. However, reliable production-scale cGMP-compliant automated procedures for [(18)F]FSPG production are still lacking to further increase the utility and clinical adoption of this radiotracer. Herein, we report the optimized automated approaches to produce [(18)F]FSPG through two commercially available radiosynthesizers capable of supporting centralized and large-scale production for clinical use. RESULTS: Starting with activity levels of 60–85 GBq, the fully-automated process to produce [(18)F]FSPG took less than 45 min with average radiochemical yields of 22.56 ± 0.97% and 30.82 ± 1.60% (non-decay corrected) using TRACERlab™ FXFN and FASTlab™, respectively. The radiochemical purities were > 95% and the formulated [(18)F]FSPG solution was determined to be sterile and colorless with the pH of 6.5–7.5. No radiolysis of the product was observed up to 8 h after final batch formulation. CONCLUSIONS: In summary, cGMP-compliant radiosyntheses and quality control of [(18)F]FSPG have been established on two commercially available synthesizers leveraging high activity concentration and radiochemical purity. While the clinical trials using [(18)F]FSPG PET are currently underway, the automated approaches reported herein will accelerate the clinical adoption of this radiotracer and warrant centralized and large-scale production of [(18)F]FSPG. Springer International Publishing 2023-07-24 /pmc/articles/PMC10366059/ /pubmed/37486582 http://dx.doi.org/10.1186/s41181-023-00200-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Methodology Lin, Mai Ta, Robert T. Manning, H. Charles Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies |
title | Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies |
title_full | Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies |
title_fullStr | Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies |
title_full_unstemmed | Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies |
title_short | Simplified and highly-reliable automated production of [(18)F]FSPG for clinical studies |
title_sort | simplified and highly-reliable automated production of [(18)f]fspg for clinical studies |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366059/ https://www.ncbi.nlm.nih.gov/pubmed/37486582 http://dx.doi.org/10.1186/s41181-023-00200-8 |
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