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A solid-phase technique for preparation of no-carrier-added technetium-99m radiopharmaceuticals: application to the streptavidin/biotin system

A high effective specific activity (HESA) formulation of a biotin-containing 99mTc ligand [RP488: dimethyl-Gly-Ser-Cys(Acm)-Lys(Biotin)-Gly] conveniently prepared from solid phase was compared to a typical low effective specific activity (LESA) solution formulation to demonstrate improved targeting...

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Bibliographic Details
Published in:Nuclear medicine and biology 2000-11, Vol.27 (8), p.803-807
Main Authors: Dunn-Dufault, Robert, Pollak, Alfred, Fitzgerald, Jane, Thornback, John R, Ballinger, James R
Format: Article
Language:English
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Summary:A high effective specific activity (HESA) formulation of a biotin-containing 99mTc ligand [RP488: dimethyl-Gly-Ser-Cys(Acm)-Lys(Biotin)-Gly] conveniently prepared from solid phase was compared to a typical low effective specific activity (LESA) solution formulation to demonstrate improved targeting to streptavidin in an in vitro assay and in an in vivo rat model. RP488 was coupled to a maleimide-functionalized polyethylene glycol resin via a thiol ether linkage and labeled with 99mTc-gluconate at room temperature, followed by elution of the HESA 99mTc-RP488 in saline (minimum specific activity ∼ 1000 TBq/mmol by amino acid analysis). Both HESA and LESA 99mTc-RP488 labeled at > 90% purity. In vitro, HESA 99mTc-RP488 incubated with streptavidin-agarose was bound quantitatively, but there was competition from addition of increasing amounts of cold RP488. In rats, radiotracer uptake was evident at the site of implantation of streptavidin-agarose beads for the HESA dose, less uptake of low effective specific activity (LESA) material, and no appreciable uptake in the control rats of the LESA or HESA dose. The target-to-background ratio for HESA 99mTc-RP488 was 5.4 times that of the control. The solid-phase technology offers a convenient way to prepare high specific activity receptor-targeting 99mTc radiopharmaceuticals.
ISSN:0969-8051
1872-9614
DOI:10.1016/S0969-8051(00)00156-6