Abstract
In this study, Lu-177-(4-{[(bis(phosphonomethyl))-carbamoyl] methyl}-7,10-bis(carboxymethyl)-1,4,7,10-tetraaza-cyclododec-1-yl) acetic acid (Lu-177-BPAMD) was successfully prepared. The quality control, partition coefficient, hydroxyapatite binding assay and stability of the complex were determined. For better comparison, biodistribution patterns of Lu-177-BPAMD and Lu-177-EDTMP complexes were compared in same animal model. Lu-177-BPAMD was prepared with high radiochemical purity (>93 %) and specific activity of 534 GBq/mmol at the optimal conditions. Comparative study between Lu-177-BPAMD and Lu-177-EDTMP indicated higher bone uptake and lesser accumulation in the other organs for Lu-177-BPAMD. Lu-177-BPAMD can be considered as a promising agent for bone pain palliation in the near future.
| Original language | English |
|---|---|
| Pages (from-to) | 1243-1251 |
| Number of pages | 9 |
| Journal | Journal of Radioanalytical and Nuclear Chemistry |
| Volume | 307 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Feb 2016 |
| Externally published | Yes |
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