Literature DB >> 11922419

Electrochemical cell for separation of [18F]fluoride from irradiated 18O-water and subsequent no carrier added nucleophilic fluorination.

K Hamacher1, Th Hirschfelder, H H Coenen.   

Abstract

An electrochemical cell was designed allowing the anodic deposition of n.c.a. [18F]fluoride solubilized in an 18O-water target and subsequent n.c.a. nucleophilic 18F-fluorination. The recovery of the deposited [18F]fluoride can be achieved in the presence of an aprotic solvent containing a phase-transfer catalyst (PTC). The radioisotope adsorbed electrochemically at the cylindrical surface of a glassy carbon electrode can be dried easily by washing the cell twice with dry aprotic solvents while maintaining a low electric field. This simple washing step makes an azeotropic drying process obsolete. Accordingly, less basic cryptates like [K within 2.2.2.]oxalate or triflate can be used for nucleophilic 18F-fluorination because loss of activity as a consequence of azeotropic drying under conditions of low basicity does not occur. The usefulness of this technique is exemplified for the n.c.a. synthesis of various 18F-labelled compounds. The radiotracers were synthesized with higher radiochemical yields and under much easier conditions than the conventional 18F-fluorination procedure which includes an additional drying step of the PTC.

Entities:  

Year:  2002        PMID: 11922419     DOI: 10.1016/s0969-8043(01)00156-7

Source DB:  PubMed          Journal:  Appl Radiat Isot        ISSN: 0969-8043            Impact factor:   1.513


  3 in total

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

Authors:  Saman Sadeghi; Vincent Liang; Shilin Cheung; Suh Woo; Curtis Wu; Jimmy Ly; Yuliang Deng; Mark Eddings; R Michael van Dam
Journal:  Appl Radiat Isot       Date:  2013-02-13       Impact factor: 1.513

Review 2.  18F-labelled intermediates for radiosynthesis by modular build-up reactions: newer developments.

Authors:  Johannes Ermert
Journal:  Biomed Res Int       Date:  2014-06-23       Impact factor: 3.411

3.  Synthesis of no-carrier-added 4-[18F]fluorophenol from 4-benzyloxyphenyl-(2-thienyl)iodonium bromide.

Authors:  Tobias L Ross; Johannes Ermert; Heinz H Coenen
Journal:  Molecules       Date:  2011-09-06       Impact factor: 4.411

  3 in total

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