A spot test for determination of residual TBA levels in 18 F-radiotracers for human use using Dragendorff reagent
When utilizing [ F]tetrabutylammonium fluoride ([ F]TBAF) in the synthesis of F-labeled radiotracers for clinical positron emission tomography (PET) imaging, it is necessary to confirm that residual TBA levels in formulated doses do not exceed established specifications (≤2.6 mg per patient dose). H...
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Published in: | Analytical methods Vol. 12; no. 41; p. 5004 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
30-10-2020
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Subjects: | |
Online Access: | Get more information |
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Summary: | When utilizing [
F]tetrabutylammonium fluoride ([
F]TBAF) in the synthesis of
F-labeled radiotracers for clinical positron emission tomography (PET) imaging, it is necessary to confirm that residual TBA levels in formulated doses do not exceed established specifications (≤2.6 mg per patient dose). Historically this has been accomplished using HPLC, but this is time consuming for short-lived PET radiotracers and limited by the need for expensive equipment. This motivated us to introduce a TLC spot test for determining residual TBA, and we have developed a new method which employs the Dragendorff reagent. Herein we report details of the TLC method and use it to quantify residual TBA in different formulations of 6-[
F]fluoro-DOPA. |
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ISSN: | 1759-9679 |
DOI: | 10.1039/D0AY01565B |