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本文引用的文献

1
On chip droplet characterization: a practical, high-sensitivity measurement of droplet impedance in digital microfluidics.芯片上液滴特性分析:数字微流控中液滴阻抗的一种实用、高灵敏度测量方法。
Anal Chem. 2012 Feb 21;84(4):1915-23. doi: 10.1021/ac202715f. Epub 2012 Feb 1.
2
Micro-chemical synthesis of molecular probes on an electronic microfluidic device.电子微流控装置上分子探针的微量化学合成。
Proc Natl Acad Sci U S A. 2012 Jan 17;109(3):690-5. doi: 10.1073/pnas.1117566109. Epub 2011 Dec 30.
3
Reactivity of electrochemically concentrated anhydrous [18F]fluoride for microfluidic radiosynthesis of 18F-labeled compounds.电化学浓缩的无水[18F]氟化物用于18F标记化合物微流控放射合成的反应活性。
Appl Radiat Isot. 2012 Jan;70(1):193-9. doi: 10.1016/j.apradiso.2011.09.022. Epub 2011 Oct 8.
4
Fast production of highly reactive no-carrier-added [18F]fluoride for the labeling of radiopharmaceuticals.快速制备用于放射性药物标记的高活性无载体添加[18F]氟化物。
Angew Chem Int Ed Engl. 2010 Apr 19;49(18):3161-4. doi: 10.1002/anie.200906341.
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Electrochemical concentration of no-carrier-added [(18)F]fluoride from [(18)O]water in a disposable microfluidic cell for radiosynthesis of (18)F-labeled radiopharmaceuticals.在用于¹⁸F标记放射性药物放射性合成的一次性微流控池中,通过电化学方法从[¹⁸O]水中浓缩无载体添加的[¹⁸F]氟化物。
Appl Radiat Isot. 2010 Sep;68(9):1703-8. doi: 10.1016/j.apradiso.2010.02.005. Epub 2010 Feb 13.
6
Design and optimization of coin-shaped microreactor chips for PET radiopharmaceutical synthesis.币形微流控芯片的设计与优化用于正电子发射断层扫描放射性药物合成。
J Nucl Med. 2010 Feb;51(2):282-7. doi: 10.2967/jnumed.109.065946.
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Fast and repetitive in-capillary production of [18F]FDG.[18F]FDG在毛细血管内的快速重复生成
Eur J Nucl Med Mol Imaging. 2009 Apr;36(4):653-8. doi: 10.1007/s00259-008-0985-9. Epub 2008 Nov 27.
8
Electrochemical transfer of (18)F from (18)O water to aprotic polar solvent.(18)F从(18)O水到非质子极性溶剂的电化学转移。
Appl Radiat Isot. 2007 May;65(5):524-7. doi: 10.1016/j.apradiso.2007.01.014. Epub 2007 Feb 6.
9
No-carrier-added nucleophilic 18F-labelling in an electrochemical cell exemplified by the routine production of [18F]altanserin.以[18F]阿坦色林的常规生产为例,在电化学池中进行无载体添加的亲核18F标记。
Appl Radiat Isot. 2006 Sep;64(9):989-94. doi: 10.1016/j.apradiso.2006.03.005. Epub 2006 Jul 7.
10
Miniaturized continuous flow reaction vessels: influence on chemical reactions.小型化连续流动反应容器:对化学反应的影响
Lab Chip. 2006 Mar;6(3):329-44. doi: 10.1039/b510856j. Epub 2006 Jan 20.

用于从[¹⁸O]水中快速分离[¹⁸F]氟化物以进行¹⁸F标记示踪剂流通合成的可重复使用的电化学电池。

Reusable electrochemical cell for rapid separation of [¹⁸F]fluoride from [¹⁸O]water for flow-through synthesis of ¹⁸F-labeled tracers.

作者信息

Sadeghi Saman, Liang Vincent, Cheung Shilin, Woo Suh, Wu Curtis, Ly Jimmy, Deng Yuliang, Eddings Mark, van Dam R Michael

机构信息

Crump Institute for Molecular Imaging and Department of Molecular & Medical Pharmacology, David Geffen School of Medicine, University of California, 570 Westwood Plaza, Los Angeles, CA 90095, USA.

出版信息

Appl Radiat Isot. 2013 May;75:85-94. doi: 10.1016/j.apradiso.2012.12.021. Epub 2013 Feb 13.

DOI:10.1016/j.apradiso.2012.12.021
PMID:23474380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4485997/
Abstract

A brass-platinum electrochemical micro-flow cell was developed to extract [(18)F]fluoride from an aqueous solution and release it into an organic-based solution, suitable for subsequent radio-synthesis, in a fast and reliable manner. This cell does not suffer electrode erosion and is thus reusable while operating faster by enabling increased voltages. By optimizing temperature, trapping and release potentials, flow rates, and electrode materials, an overall [(18)F]fluoride trapping and release efficiency of 84 ± 5% (n=7) was achieved. X-ray photoelectron spectroscopy (XPS) was used to analyze electrode surfaces of various metal-metal systems and the findings were correlated with the performance of the electrochemical cell. To demonstrate the reactivity of the released [(18)F]fluoride, the cell was coupled to a flow-through reactor and automated synthesis of [(18)F]FDG with a repeatable decay-corrected yield of 56 ± 4% (n=4) was completed in < 15 min. A multi-human dose of 5.92GBq [(18)F]FDG was also demonstrated.

摘要

开发了一种铜-铂电化学微流池,用于从水溶液中提取[¹⁸F]氟化物,并将其快速可靠地释放到适用于后续放射性合成的有机基溶液中。该微流池不会出现电极腐蚀问题,因此可重复使用,并且通过提高电压能够更快地运行。通过优化温度、捕获和释放电位、流速以及电极材料,实现了[¹⁸F]氟化物的总体捕获和释放效率为84±5%(n=7)。使用X射线光电子能谱(XPS)分析了各种金属-金属系统的电极表面,并将结果与电化学微流池的性能相关联。为了证明释放出的[¹⁸F]氟化物的反应活性,将该微流池与流通式反应器相连,并在不到15分钟的时间内完成了[¹⁸F]FDG的自动化合成,经衰减校正后的可重复产率为56±4%(n=4)。还展示了5.92GBq的多人体剂量[¹⁸F]FDG。