Synthesis and evaluation of potential tu
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F. C. Hunt; D. J. Maddalena; A. B. McLaren; J. G. Wilson
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Article
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1982
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John Wiley and Sons
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French
⚖ 266 KB
## Abstract To exploit the tissue affinity of compounds for radiopharmaceutical purposes, attachment of chelating groups is usually necessary to facilitate technetium‐99m binding and transport. The chelating group, iminodiacetic acid, previously used to modify lidocaine for hepatobiliary radiophar