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Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production

BACKGROUND: PET radiopharmaceutical development and the implementation of a production method on a synthesis module is a complex and time-intensive task since new synthesis methods must be adapted to the confines of the synthesis platform in use. Commonly utilized single fluid bus architectures put...

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Autores principales: Frank, Christopher, Winter, Georg, Rensei, Fredrik, Samper, Victor, Brooks, Allen F., Hockley, Brian G., Henderson, Bradford D., Rensch, Christian, Scott, Peter J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751239/
https://www.ncbi.nlm.nih.gov/pubmed/31659546
http://dx.doi.org/10.1186/s41181-019-0077-0
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author Frank, Christopher
Winter, Georg
Rensei, Fredrik
Samper, Victor
Brooks, Allen F.
Hockley, Brian G.
Henderson, Bradford D.
Rensch, Christian
Scott, Peter J. H.
author_facet Frank, Christopher
Winter, Georg
Rensei, Fredrik
Samper, Victor
Brooks, Allen F.
Hockley, Brian G.
Henderson, Bradford D.
Rensch, Christian
Scott, Peter J. H.
author_sort Frank, Christopher
collection PubMed
description BACKGROUND: PET radiopharmaceutical development and the implementation of a production method on a synthesis module is a complex and time-intensive task since new synthesis methods must be adapted to the confines of the synthesis platform in use. Commonly utilized single fluid bus architectures put multiple constraints on synthesis planning and execution, while conventional microfluidic solutions are limited by compatibility at the macro-to-micro interface. In this work we introduce the ISAR synthesis platform and custom-tailored fluid paths leveraging up to 70 individually addressable valves on a chip-based consumable. The ISAR synthesis platform replaces traditional stopcock valve manifolds with a fluidic chip that integrates all fluid paths (tubing) and valves into one consumable and enables channel routing without the single fluid bus constraint. ISAR can scale between the macro- (10 mL), meso- (0.5 mL) and micro- (≤0.05 mL) domain seamlessly, addressing the macro-to-micro interface challenge and enabling custom tailored fluid circuits for a given application. In this paper we demonstrate proof-of-concept by validating a single chip design to address the challenge of synthesizing multiple batches of [(13)N]NH(3) for clinical use throughout the workday. RESULTS: ISAR was installed at an academic PET Center and used to manufacture [(13)N]NH(3) in > 96% radiochemical yield. Up to 9 batches were manufactured with a single consumable chip having parallel paths without the need to open the hot-cell. Quality control testing confirmed the ISAR-based [(13)N]NH(3) met existing clinical release specifications, and utility was demonstrated by imaging a rodent with [(13)N]NH(3) produced on ISAR. CONCLUSIONS: ISAR represents a new paradigm in radiopharmaceutical production. Through a new system architecture, ISAR integrates the principles of microfluidics with the standard volumes and consumables established in PET Centers all over the world. Proof-of-concept has been demonstrated through validation of a chip design for the synthesis of [(13)N]NH(3) suitable for clinical use.
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spelling pubmed-67512392019-10-04 Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production Frank, Christopher Winter, Georg Rensei, Fredrik Samper, Victor Brooks, Allen F. Hockley, Brian G. Henderson, Bradford D. Rensch, Christian Scott, Peter J. H. EJNMMI Radiopharm Chem Research Article BACKGROUND: PET radiopharmaceutical development and the implementation of a production method on a synthesis module is a complex and time-intensive task since new synthesis methods must be adapted to the confines of the synthesis platform in use. Commonly utilized single fluid bus architectures put multiple constraints on synthesis planning and execution, while conventional microfluidic solutions are limited by compatibility at the macro-to-micro interface. In this work we introduce the ISAR synthesis platform and custom-tailored fluid paths leveraging up to 70 individually addressable valves on a chip-based consumable. The ISAR synthesis platform replaces traditional stopcock valve manifolds with a fluidic chip that integrates all fluid paths (tubing) and valves into one consumable and enables channel routing without the single fluid bus constraint. ISAR can scale between the macro- (10 mL), meso- (0.5 mL) and micro- (≤0.05 mL) domain seamlessly, addressing the macro-to-micro interface challenge and enabling custom tailored fluid circuits for a given application. In this paper we demonstrate proof-of-concept by validating a single chip design to address the challenge of synthesizing multiple batches of [(13)N]NH(3) for clinical use throughout the workday. RESULTS: ISAR was installed at an academic PET Center and used to manufacture [(13)N]NH(3) in > 96% radiochemical yield. Up to 9 batches were manufactured with a single consumable chip having parallel paths without the need to open the hot-cell. Quality control testing confirmed the ISAR-based [(13)N]NH(3) met existing clinical release specifications, and utility was demonstrated by imaging a rodent with [(13)N]NH(3) produced on ISAR. CONCLUSIONS: ISAR represents a new paradigm in radiopharmaceutical production. Through a new system architecture, ISAR integrates the principles of microfluidics with the standard volumes and consumables established in PET Centers all over the world. Proof-of-concept has been demonstrated through validation of a chip design for the synthesis of [(13)N]NH(3) suitable for clinical use. Springer International Publishing 2019-09-18 /pmc/articles/PMC6751239/ /pubmed/31659546 http://dx.doi.org/10.1186/s41181-019-0077-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Frank, Christopher
Winter, Georg
Rensei, Fredrik
Samper, Victor
Brooks, Allen F.
Hockley, Brian G.
Henderson, Bradford D.
Rensch, Christian
Scott, Peter J. H.
Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production
title Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production
title_full Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production
title_fullStr Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production
title_full_unstemmed Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production
title_short Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production
title_sort development and implementation of isar, a new synthesis platform for radiopharmaceutical production
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751239/
https://www.ncbi.nlm.nih.gov/pubmed/31659546
http://dx.doi.org/10.1186/s41181-019-0077-0
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