Abstract
A skeletal seeking radiopharmaceutical labeled with a long-lived radionuclide was developed to evaluate regional bone formation and its subsequent resorption. The agent is [phosphonate (phenylmethylene hydroxy) bis]-I-125 or I-125 θPA. Tissue distribution studies in mice (N=16) showed approximately 40% of the administered dose to be retained by the skeleton up to 336 hours post IV injection. The percentage of the dose accumulated by the thyroid gland remained at less than 0.5%, indicating minimal deiodination of the I-125 θPA. Whole body retention studies in the same species revealed a triexponential release pattern with the longest component comprising 33% of the dose with a biologic half-life of 962 days. A fractured rat tibia model was studied with I-125 θPA and Tc-99m MDP. Chronic loss of the I-125 θPA relative to normal tibia was quantitated: five days (62.8%); 30 days (47.4%). Concomitant increased uptake of the Tc-99m MDP was observed at the fracture site relative to normal: five days (186%); 30 days (1,041%). The above data suggest that I-125 θPA can be utilized to measure acute bone formation and chronic resorption.
Original language | English |
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Pages (from-to) | 233-237 |
Number of pages | 5 |
Journal | Skeletal Radiology |
Volume | 7 |
Issue number | 4 |
DOIs | |
State | Published - Jan 1982 |
Externally published | Yes |
Keywords
- I-125
- I-125 θPA
- Phosphonate (phenyl-methylene hydroxy) bis
- Radiopharmaceutical
- Skeletal resorption
- Tc-99 MDP