Published 1979 | Version v1
Report Open

Synthesis of [18F]-5-fluorouridine (F-18-5-FUR) as a probe for measuring RNA synthesis and tumor growth rates in vivo

Description

A method for the rapid synthesis of high specific activity of [18F]-5-fluorouridine is described. The 20Ne(d,α)18F nuclear reaction is used to produce high specific activity, anhydrous [18F]-F2 at the Brookhaven National Laboratory 60'' cyclotron. Fluorination of 2',3',5'-tri-0-acetyluridine with [18F]-F2 in glacial acetic acid at room temperature followed by hydrolysis with sodium methoxide in methanol gives [18F]-5-fluorouridine with a radiochemical yield of 5 to 7% in a synthesis time of 90 minutes from EOB. The compound is required for the study of RNA synthesis and tumor growth rates in vivo

Availability note (English)

MF available from INIS under the Report Number; Available from NTIS., PC A02/MF A01.

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Additional details

Publishing Information

Imprint Pagination
8 p.
Report number
BNL--25851

Conference

Title
2. international symposium on radiopharmaceuticals.
Dates
18 - 23 Mar 1979.
Place
Seattle, WA, USA.

Optional Information

Secondary number(s)
CONF-790321--7.