Synthesis and radioiodination of ten aryl-carbohydrate compounds for labeling monoclonal antibodies
β Scribed by S. D. Warren; S. A. Ali; K. Y. Richter; K. A. Krohn
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 592 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
Ten arylβcarbohydrate ligands have been synthesized that potentially increase the tumor retention and decrease the deiodination of iodinated monoclonal antibodies used in the imaging and treatment of cancer. The compounds were synthesized via reductive amination reactions, purified with cation exchange chromatography, and characterized using ^1^H and ^13^C NMR. These compounds were then radioiodinated to assess their iodination characteristics, for subsequent experiments involving attachment to monoclonal antibodies.
π SIMILAR VOLUMES
The synthesis of new linked bis-and tris-ring tetraazamacrocyclic (bifunctional) reagents for use in an alternative strategy for radiolabelling antibodies is described. For comparison with the above systems, a new single ring bifunctional system incorporating a dioxocyclam ring is also reported.