Panel Disdussion
Panel Disdussion
Panel Disdussion
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3rd International Congress of of Nuclear Medicine & & 15th 15th Iranian Annual Annual Congress of<br />
Congress of Nuclear Medicine<br />
Shahid Beheshti Shahid Beheshti University University of Medical of Medical Sciences Sciences 19-21 19-21 May May 2011<br />
Development of an in vivo radionuclide generator by labeling<br />
Bleomycin with 191Os<br />
Leila Moghaddam-Banaem 1 , Amir Reza Jalilian 1 , Mina Jamreh 2 ,<br />
Nafiseh Salek 2 , Mojtaba Shamsaee 2<br />
1 Radiopharmaceutical Research and Development Lab (RRDL)<br />
2 Faculty of Nuclear Engineering and Physics-AmirKabir Technical University<br />
Bleomycin (BLM) has been labeled with various radioisotopes and<br />
widely used in therapy and diagnosis. 191Osmium is a parent<br />
radionuclide with 15.4d half-life and decays by beta emission to<br />
191mIridium which is a radionuclide with 4.96s half-life. It decays by<br />
isometric transition to stable 191Ir, emitting a 129-keV gamma<br />
photon. In this study BLM was labeled with 191Os-hexachloro-osmate<br />
and its distribution and stability in mice was determined. The<br />
complex was obtained at the pH=2 in normal saline at 90°C in 60<br />
minutes. Radio-TLC showed an overall radiochemical yield of 95-97%<br />
(radiochemical purity >97%). The biodistribution studies for 191Os<br />
and 191Os -BLM were carried out in mice up to 15d. Liver and spleen<br />
uptake increased 24-48 hours after administration of 191Os-BLM.<br />
Lung uptake increased after 48 hours. Twenty four hours after<br />
administration, the radioactivity of the bladder and kidney increased<br />
and remained constant. This research introduces 191Os-BLM in<br />
therapeutic studies as an in-vivo generator for therapy because of<br />
beta emissions and also for localization and dosimetry study in<br />
relevant organs by gamma emission of the daughter radio-nuclide.<br />
Keywords: 191Osmium-Bleomycin, Labeling, Biodistribution<br />
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