Published 1990 | Version v1
Report

The sequential production of [18F]-6-FDOPA and [18F]-F-m-TYROSINE (or [18F]-2-FDG) from the same dilute [18F]F2 target gas

  • 1. McMaster Univ., Hamilton, Ontario (Canada)
  • 2. Chedoke-McMaster Hospitals, Hamilton, Ontario (Canada)

Description

The recovery of [18F] from the target is 65 ± 8% when 0.4% F2 in neon is the target gas. The fraction of [18F] trapped in the reaction vessel during direct fluorination of aromatic compounds is dependent upon the solvent used for the reaction. For the fluorination of L-DOPA in HF/BF3, the [18F] trapped in the reaction vessel is 36 ± 4% whereas in other solvents it is 60 ± 5%. The percent recovery of [18F] is even lower for less activated aromatic rings such as ortho, meta and para-tyrosine in HF/BF3 (12-16%). The aim of this work is to demonstrate how to utilize this unreacted, readily available, [18F]F2 for developmental work

Additional details

Publishing Information

Imprint Title
Eighth international symposium on radiopharmaceutical chemistry. Abstracts: Final report
Imprint Pagination
458 p.
Journal Page Range
p. 294-295.
Report number
DOE/ER/60968--1

Conference

Title
8. international symposium on radiopharmaceutical chemistry.
Dates
24-29 Jun 1990.
Place
Princeton, NJ (United States).

Optional Information

Secondary number(s)
CONF-9006363--Absts.