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Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor

Microfluidics offers numerous advantages for the synthesis of short-lived radiolabeled imaging tracers: performing (18)F-radiosyntheses in microliter-scale droplets has exhibited high efficiency, speed, and molar activity as well as low reagent consumption. However, most reports have been at the pre...

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Autores principales: Wang, Jia, Chao, Philip H., Slavik, Roger, van Dam, R. Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049805/
https://www.ncbi.nlm.nih.gov/pubmed/35492189
http://dx.doi.org/10.1039/d0ra01212b
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author Wang, Jia
Chao, Philip H.
Slavik, Roger
van Dam, R. Michael
author_facet Wang, Jia
Chao, Philip H.
Slavik, Roger
van Dam, R. Michael
author_sort Wang, Jia
collection PubMed
description Microfluidics offers numerous advantages for the synthesis of short-lived radiolabeled imaging tracers: performing (18)F-radiosyntheses in microliter-scale droplets has exhibited high efficiency, speed, and molar activity as well as low reagent consumption. However, most reports have been at the preclinical scale. In this study we integrate a [(18)F]fluoride concentrator and a microdroplet synthesizer to explore the possibility of synthesizing patient doses and multi-patient batches of clinically-acceptable tracers. In the integrated system, [(18)F]fluoride (up to 41 GBq [1.1 Ci]) in [(18)O]H(2)O (1 mL) was first concentrated ∼80-fold and then efficiently transferred to the 8 μL reaction chip as a series of small (∼0.5 μL) droplets. Each droplet rapidly dried at the reaction site of the pre-heated chip, resulting in localized accumulation of large amounts of radioactivity in the form of dried [(18)F]TBAF complex. The PET tracer [(18)F]fallypride was synthesized from this concentrated activity in an overall synthesis time of ∼50 min (including radioisotope concentration and transfer, droplet radiosynthesis, purification, and formulation), in amounts up to 7.2 GBq [0.19 Ci], sufficient for multiple clinical PET scans. The resulting batches of [(18)F]fallypride passed all QC tests needed to ensure safety for clinical injection. This integrated technology enabled for the first time the impact of a wide range of activity levels on droplet radiosynthesis to be studied. Furthermore, this substantial increase in scale expands the applications of droplet radiosynthesis to the production of clinically-relevant amounts of radiopharmaceuticals, and potentially even centralized production of clinical tracers in radiopharmacies. The overall system could be applied to fundamental studies of droplet-based radiochemical reactions, or to the production of radiopharmaceuticals labeled with a variety of isotopes used for imaging and/or targeted radiotherapeutics.
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spelling pubmed-90498052022-04-29 Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor Wang, Jia Chao, Philip H. Slavik, Roger van Dam, R. Michael RSC Adv Chemistry Microfluidics offers numerous advantages for the synthesis of short-lived radiolabeled imaging tracers: performing (18)F-radiosyntheses in microliter-scale droplets has exhibited high efficiency, speed, and molar activity as well as low reagent consumption. However, most reports have been at the preclinical scale. In this study we integrate a [(18)F]fluoride concentrator and a microdroplet synthesizer to explore the possibility of synthesizing patient doses and multi-patient batches of clinically-acceptable tracers. In the integrated system, [(18)F]fluoride (up to 41 GBq [1.1 Ci]) in [(18)O]H(2)O (1 mL) was first concentrated ∼80-fold and then efficiently transferred to the 8 μL reaction chip as a series of small (∼0.5 μL) droplets. Each droplet rapidly dried at the reaction site of the pre-heated chip, resulting in localized accumulation of large amounts of radioactivity in the form of dried [(18)F]TBAF complex. The PET tracer [(18)F]fallypride was synthesized from this concentrated activity in an overall synthesis time of ∼50 min (including radioisotope concentration and transfer, droplet radiosynthesis, purification, and formulation), in amounts up to 7.2 GBq [0.19 Ci], sufficient for multiple clinical PET scans. The resulting batches of [(18)F]fallypride passed all QC tests needed to ensure safety for clinical injection. This integrated technology enabled for the first time the impact of a wide range of activity levels on droplet radiosynthesis to be studied. Furthermore, this substantial increase in scale expands the applications of droplet radiosynthesis to the production of clinically-relevant amounts of radiopharmaceuticals, and potentially even centralized production of clinical tracers in radiopharmacies. The overall system could be applied to fundamental studies of droplet-based radiochemical reactions, or to the production of radiopharmaceuticals labeled with a variety of isotopes used for imaging and/or targeted radiotherapeutics. The Royal Society of Chemistry 2020-02-24 /pmc/articles/PMC9049805/ /pubmed/35492189 http://dx.doi.org/10.1039/d0ra01212b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Jia
Chao, Philip H.
Slavik, Roger
van Dam, R. Michael
Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor
title Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor
title_full Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor
title_fullStr Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor
title_full_unstemmed Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor
title_short Multi-GBq production of the radiotracer [(18)F]fallypride in a droplet microreactor
title_sort multi-gbq production of the radiotracer [(18)f]fallypride in a droplet microreactor
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049805/
https://www.ncbi.nlm.nih.gov/pubmed/35492189
http://dx.doi.org/10.1039/d0ra01212b
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