Synthesis of a 188Re–HEDP Complex Using Carrier-Free 188Re and a Study of Its Stability and Biological Distribution
Radiochemistry • 2011
Publication Information
Authors
M. Y. Nassar, M. T. El-Kolaly, and M. R. H. Mahran
Keywords
Not Available
Journal
Radiochemistry
Publisher
Pleiades
Volume
53
Issue
4
Pages
415-420
publication.type
International
Paper Link
Open Link
Supplementary Materials
Not Available
Abstract
Labeling of disodium dihydrogen 1-hydroxyethane-1,1-diphosphonate (HEDP) with 188Re was
studied. Stannous chloride was used as a reducing agent for the reduction of 188ReO4
–. The dependence of the
yield of 188Re–HEDP complex upon the HEDP concentration, tin(II) content, reaction time, amount of antioxidant,
pH, reaction temperature, and presence of carrier was examined. The optimum conditions ensuring high
labeling yield of 188Re–HEDP complex (91.0% with carrier-free Re and 96.5% with carrier-added Re) are as
follows: 15 mg of HEDP, 2 mg of Sn(II), 4 mg of ascorbic acid, pH 1.2, 100°C, 10 min. The amount of the
carrier added is 200 μg of KReO4. The 188Re–HEDP complex prepared at 100°C is more stable than that prepared
at 30°C, and the carrier-added 188Re–HEDP complex is more stable than the no-carrier-added complex.
studied. Stannous chloride was used as a reducing agent for the reduction of 188ReO4
–. The dependence of the
yield of 188Re–HEDP complex upon the HEDP concentration, tin(II) content, reaction time, amount of antioxidant,
pH, reaction temperature, and presence of carrier was examined. The optimum conditions ensuring high
labeling yield of 188Re–HEDP complex (91.0% with carrier-free Re and 96.5% with carrier-added Re) are as
follows: 15 mg of HEDP, 2 mg of Sn(II), 4 mg of ascorbic acid, pH 1.2, 100°C, 10 min. The amount of the
carrier added is 200 μg of KReO4. The 188Re–HEDP complex prepared at 100°C is more stable than that prepared
at 30°C, and the carrier-added 188Re–HEDP complex is more stable than the no-carrier-added complex.
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