## Abstract An efficient preparation of __N__‐succinimidyl 4‐[^18^F]fluorobenzoate ([^18^F]SFB) based on a convenient three‐step, one‐pot procedure is described. [^18^F]Fluorination of the precursor ethyl 4‐(trimethylammonium triflate)benzoate gave ethyl 4‐[^18^F]fluorobenzoate. Saponification of t
Two-step radiosynthesis of [18F]N-succinimidyl-4-fluorobenzoate ([18F]SFB)
✍ Scribed by Matthias Glaser; Erik Årstad; Sajinder K. Luthra; Edward G. Robins
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- French
- Weight
- 141 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The acylation reagent [^18^F]N‐succinimidyl‐4‐fluorobenzoate (^18^F‐SFB) has been prepared using a new two‐step approach. The starting material p‐[^18^F]fluorobenzaldehyde (^18^F‐FBA) was obtained by an improved radiosynthesis with a decay‐corrected radiochemical yield of 66±6 % (n=3). Reaction of ^18^F‐FBA with (diacetoxyiodine)benzene and N‐hydroxysuccinimide and preparative HPLC purification furnished ^18^F‐SFB in an r.c.y. of 49±6 % (n=3), based on the starting radioactivity of ^18^F‐FBA. The radiochemical purity of ^18^F‐SFB was >99%. Alternatively, purification by solid phase extraction gave ^18^F‐SFB with an r.c.y. of 77±9% (n=4) and a radiochemical purity of 89±5% (n=4). This radiochemical synthesis only used non‐aqueous solvents, which simplifies the method and facilitates subsequent applications of ^18^F‐SFB. Copyright © 2009 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract The batch microfluidic technology is a promising system for sequential chemical steps combining the advantages of micro‐scale reactions, while addressing some shortcomings of flow‐through systems. We report herein the convenient three‐step, one‐pot synthesis and purification of [^18^F]S
## Abstract A fully automated synthesis of __N__‐succinimidyl 4‐[^18^F]fluorobenzoate ([^18^F]SFB) was carried out by a convenient three‐step, one‐pot procedure on the modified TRACERlab FX~FN~ synthesizer, including [^18^F]fluorination of ethyl 4‐(trimethylammonium triflate)benzoate as the precurs
## Abstract A General Electric Medical Systems (GEMS) Tracerlab FX~FN~ fluorine‐18 synthesis module has been reconfigured to allow rapid (45 min), fully automated production of __N__‐succinimidyl 4‐[^18^F]fluorobenzoate ([^18^F]SFB) using the established three‐step, one‐pot synthesis procedure. Pur
## Abstract Three G‐rich oligonucleotides (GROs) were conjugated with N‐succinimidyl 4‐[^18^F]fluorobenzoate (S^18^FB). The yields for GRO5, the shortest sequence among those three GROs being tested, were 42, 70, 84, and 99% at GRO5 concentration of 59, 118, 236, and 472 nmol/100 µl, respectively.
## Abstract We have labeled proinsulin connecting peptide (C‐peptide) with fluorine‐18 (__t__~½~=109.7 min) in order to perform __in vivo__ biodistribution and pharmacokinetic studies with position emission tomography (PET). This study reports the optimization of the conjugation labeling in the N‐t