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使用激光微加工阴离子交换微柱进行高效[F]氟化物预浓缩

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

作者信息

Gomes Antonio Arleques, Nario Arian Pérez, Lapolli André Luis, Samad Ricardo Elgul, Bernardes Emerson Soares, de Rossi Wagner

机构信息

Instituto de Pesquisas Energéticas e Nucleares (IPEN-CNEN-SP), São Paulo, SP, CEP 05508-000, Brazil.

出版信息

EJNMMI Radiopharm Chem. 2025 Mar 21;10(1):11. doi: 10.1186/s41181-025-00334-x.

DOI:10.1186/s41181-025-00334-x
PMID:40113734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11926312/
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 [F]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 [F]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 KCO for [F]fluoride elution. This solution was employed directly in the radiosynthesis of [F]fluoromisonidazole ([F]FMISO), resulting in a 100% radiochemical conversion (RCC) to THP-protected [F]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.

摘要

背景

在过去十年中,标记有氟 - 18的放射性药物在非侵入性成像,特别是正电子发射断层扫描(PET)中的使用显著增加。然而,大多数情况下传统的亲核氟化合成方法需要共沸干燥步骤,这会导致活性损失并增加合成时间。微流控装置具有反应时间短、洗脱效率高和试剂用量减少等优点。

结果

我们开发了一种用于[F]氟化物捕获和洗脱的新型微柱,它是使用超短激光脉冲加工在硼硅酸盐光学玻璃(BK7)中蚀刻而成。该微柱的珠粒体积为17 μL,阴离子交换树脂的最大容量为8.5 mg。该微柱无需QMA预处理,使用超过123 GBq的[F]氟化物时,总体捕获效率和回收率(RE)为(94.09 ± 0.12)%。该回收率是使用100 μL含有Kryptofix 2.2.2的无水乙腈标准溶液获得的,该溶液仅含5 μL水和5.4 μmol用于[F]氟化物洗脱的KCO。该溶液直接用于[F]氟米索硝唑([F]FMISO)的放射性合成,在110°C下10分钟内实现了100%的放射化学转化率(RCC),生成THP保护的[F]FMISO。

结论

所开发的微柱为将微流控芯片集成到传统盒式装置中提供了一种新型工具,有助于更高效地制备放射性药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/79e9f40054f6/41181_2025_334_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/c3da8152653b/41181_2025_334_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/f75adfc3a277/41181_2025_334_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/5f49fbeaac18/41181_2025_334_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/4787072c4fd2/41181_2025_334_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/79e9f40054f6/41181_2025_334_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/c3da8152653b/41181_2025_334_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/f75adfc3a277/41181_2025_334_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/5f49fbeaac18/41181_2025_334_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/4787072c4fd2/41181_2025_334_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b76/11926312/79e9f40054f6/41181_2025_334_Fig5_HTML.jpg

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State of the art procedures towards reactive [F]fluoride in PET tracer synthesis.
正电子发射断层显像(PET)示踪剂合成中针对活性[F]氟化物的先进程序。
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