Production, quality control and biological evaluation of 153Sm-TTHMP as a possible bone palliation agent

نویسندگان

  • Ali Bahrami-Samani Radiopharmaceutical Research and Development Lab, Nuclear Science and Technology Research Institute, Atomic Energy Organization of Iran, Tehran, Iran
  • Ali Nemati Kharat Inorganic Chemistry Department, Faculty of Sciences, Tehran University, Tehran, Iran
  • Amir Reza Jalilian Radiopharmaceutical Research and Development Lab, Nuclear Science and Technology Research Institute, Atomic Energy Organization of Iran, Tehran, Iran
  • Mohammad Ghannadi-Maragheh Radiopharmaceutical Research and Development Lab, Nuclear Science and Technology Research Institute, Atomic Energy Organization of Iran, Tehran, Iran
  • Zohreh Naseri Inorganic Chemistry Department, Faculty of Sciences, Tehran University, Tehran, Iran
چکیده مقاله:

Introduction: Various bone palliative therapeutic agents have been developed and widely used for bone metastasis such as 153Sm-EDTMP. In this study, production, quality control and biodistribution studies of a newly developed therapeutic compound have been presented followed by imaging studies in wild-type rodents. Methods: 153Sm-TTHMP was prepared starting from 153Sm-SmCl3, prepared by neutron activation of an enriched 152Sm sample (purity >98%), and in-house synthesized TTHMP in 1h at 25°C followed by stability tests, partition coefficient determination and biodistribution studies of in wild-type rodents using scarification and SPECT imaging. Results: The radiolabled Sm complex was prepared in high radiochemical purity (>99%, ITLC) and specific activity of 278 GBq/mmol and demonstrated significant stability at 4, 25 and 37°C (in presence of human serum). Initial biodistribution data showed significant bone accumulation of the tracer in 48h. Conclusion: 153Sm-TTHMP can be a potential candidate for bone pain palliation therapy in skeletal metastases, although further biological studies in other mammals is still needed.

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عنوان ژورنال

دوره 19  شماره 2

صفحات  60- 68

تاریخ انتشار 2011-12-01

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