D. Bender et Ad. Gee, SOLID PHASE-SUPPORTED REACTION OF NCA (HCN)-C-11 WITH ARABINOSE - A SIMPLIFIED AUTOMATED SYNTHESIS OF D-[1-C-11]GLUCOSE, Journal of labelled compounds & radiopharmaceuticals, 41(4), 1998, pp. 287-300
Citations number
30
Categorie Soggetti
Chemistry Analytical","Chemistry Medicinal","Biochemical Research Methods
A simplified, automated synthesis for D-[1-C-11]glucose is described b
y the solid phase-supported reaction of (NH4CN)-C-11 with D-arabinose
on an Alumina N Sep-Pak(TM). C-11-cyanide reacted instantaneously to p
roduce [1-C-11]aldonitriles. Reduction with Raney nickel in formic aci
d and semipreparative HPLC afforded D-[1-C-11]glucose with radiochemic
al purity >95%. Compared with previously reported procedures a pH adju
stment and rotary evaporation step is avoided resulting in a shortenin
g of the synthesis time from 55 to 38 min. The radiochemical yield was
5 - 15% (2.5 - 8.5% non-corrected) based on (NH4CN)-C-11. For a typic
al production starting with 20 GBq of (NH4CN)-C-11 up to 500 MBq D-[1-
C-11]glucose was obtained at end of synthesis as a sterile, formulated
solution.