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Effect of structural modifications on the adrenal uptake of steroids labeled in the side chain with tellurium-123m

Journal Article · · J. Nucl. Med.; (United States)
OSTI ID:5409772

A series of structurally modified steroids labeled in the side chain with Te-123m have been prepared and tested in rats to determine the critical structural features required for maximal adrenal uptake of this new class of potential adrenal-imaging agents. The Te-123m steroids investigated contained structural modifications of both the nucleus and side chain. Tissue distribution experiments and rectilinear scans indicated that 23-(isopropyl telluro)-24-nor-5..cap alpha..-cholan-3..beta..-ol (saturated nucleus), and 24-(isopropyl telluro)-chol-5-en-3..beta..-ol (nuclear double bond) showed pronounced adrenal uptake after 1 day, with adrenal-to-liver ratios of 41 and 27, respectively. These results indicate that a combination of structural features is required for significant adrenal uptake of steroids labeled in the side chain with Te-123m. The structural requirements include a trans ring structure, an equatorial C-3 hydroxyl group, and a 17..beta.. side chain of moderate length.

Research Organization:
Oak Ridge National Lab., TN
OSTI ID:
5409772
Journal Information:
J. Nucl. Med.; (United States), Journal Name: J. Nucl. Med.; (United States) Vol. 21:3; ISSN JNMEA
Country of Publication:
United States
Language:
English

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