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      High-efficiency [ 18F]fluoride pre-concentration using a laser-micromachined anion-exchange micro-cartridge

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          Abstract

          Background

          The use of radiopharmaceuticals labelled with fluorine-18 in non-invasive imaging, particularly in Positron Emission Tomography (PET), increased significantly during the last decade. However, traditional nucleophilic fluorination synthesis methods in most cases require azeotropic drying steps, leading to loss of activity and increased synthesis time. Microfluidic devices offer improvements with shorter reaction times, higher elution efficiency, and reduced reagent quantities.

          Results

          We developed a novel micro-cartridge for [ 18F]fluoride trapping and elution, etched in borosilicate optical glass (BK7) using ultrashort laser pulse machining. The micro-cartridge has a bead volume of 17 µL and a maximum capacity of 8.5 mg for anion exchange resin. The micro-cartridge, without the need for QMA preconditioning, exhibited an overall trapping efficiency and recovery efficiency (RE) of (94.09 ± 0.12)% using an activity exceeding 123 GBq of [ 18F]fluoride. This RE was obtained using 100 µL of a standard solution of anhydrous acetonitrile with Kryptofix 2.2.2, containing only 5 µL of water and 5.4 µmol of K 2CO 3 for [ 18F]fluoride elution. This solution was employed directly in the radiosynthesis of [ 18F]fluoromisonidazole ([ 18F]FMISO), resulting in a 100% radiochemical conversion (RCC) to THP-protected [ 18F]FMISO within 10 min at 110 °C.

          Conclusions

          The developed micro-cartridge provides a novel tool for integrating microfluidic chips into conventional cassettes, facilitating more efficient radiopharmaceutical preparation.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s41181-025-00334-x.

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          Most cited references53

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          Fluorine-18 Radiochemistry, Labeling Strategies and Synthetic Routes

          Fluorine-18 is the most frequently used radioisotope in positron emission tomography (PET) radiopharmaceuticals in both clinical and preclinical research. Its physical and nuclear characteristics (97% β+ decay, 109.7 min half-life, 635 keV positron energy), along with high specific activity and ease of large scale production, make it an attractive nuclide for radiochemical labeling and molecular imaging. Versatile chemistry including nucleophilic and electrophilic substitutions allows direct or indirect introduction of 18F into molecules of interest. The significant increase in 18F radiotracers for PET imaging accentuates the need for simple and efficient 18F-labeling procedures. In this review, we will describe the current radiosynthesis routes and strategies for 18F labeling of small molecules and biomolecules.
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            Fabrication and Applications of Microfluidic Devices: A Review

            Microfluidics is a relatively newly emerged field based on the combined principles of physics, chemistry, biology, fluid dynamics, microelectronics, and material science. Various materials can be processed into miniaturized chips containing channels and chambers in the microscale range. A diverse repertoire of methods can be chosen to manufacture such platforms of desired size, shape, and geometry. Whether they are used alone or in combination with other devices, microfluidic chips can be employed in nanoparticle preparation, drug encapsulation, delivery, and targeting, cell analysis, diagnosis, and cell culture. This paper presents microfluidic technology in terms of the available platform materials and fabrication techniques, also focusing on the biomedical applications of these remarkable devices.
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              Efficient stereospecific synthesis of no-carrier-added 2-[18F]-fluoro-2-deoxy-D-glucose using aminopolyether supported nucleophilic substitution.

              An aminopolyether mediated synthesis of fluorine-18 (18F) 2-fluoro-2-deoxy-D-glucose (FDG) has been developed. The nucleophilic fluorination with accelerator-produced [18F]fluoride works at the no-carrier-added level and gives epimerically pure 2-18FDG with an uncorrected radiochemical yield of a maximum 50% in a synthesis time of approximately 50 min from EOB.
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                Author and article information

                Contributors
                antonio.gomes@usp.br , gomesbjj.33@gmail.com
                Journal
                EJNMMI Radiopharm Chem
                EJNMMI Radiopharm Chem
                EJNMMI Radiopharmacy and Chemistry
                Springer International Publishing (Cham )
                2365-421X
                21 March 2025
                21 March 2025
                December 2025
                : 10
                : 11
                Affiliations
                Instituto de Pesquisas Energéticas e Nucleares (IPEN-CNEN—SP), ( https://ror.org/01senny43) São Paulo, SP CEP 05508–000 Brazil
                Author information
                http://orcid.org/0000-0003-3158-8217
                Article
                334
                10.1186/s41181-025-00334-x
                11926312
                40113734
                ee93844a-44ca-476d-b52f-f0bb2667f158
                © The Author(s) 2025

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

                History
                : 6 January 2025
                : 27 February 2025
                Funding
                Funded by: CNPq
                Award ID: GD 174673/2023-0
                Award ID: Sisfóton-440228/2021-2
                Award Recipient :
                Funded by: CNPq-INCTs
                Award ID: INFO-465763/2014-6
                Funded by: CNPq-INCT
                Award ID: INTERAS 406761/2022-1
                Funded by: Project COPDE
                Award ID: IPEN 2020.06.08
                Award Recipient :
                Funded by: FAPESP
                Award ID: 2013-26113-6
                Funded by: CAPES
                Award ID: Finances Code 001
                Award ID: PROEX 88887.595780/2020 00
                Categories
                Research Article
                Custom metadata
                © Springer Nature Switzerland AG 2025

                microfluidics,micro-cartridge,[18f]fluoride,positron emission tomography (pet),ultra-short laser pulse

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