Metabolic Comparison of Radiolabeled Bleomycin and Bleomycin-Glucuronide Labeled with 99mTc
dc.contributor.author | Koçan, F | |
dc.contributor.author | Avcibasi, U | |
dc.contributor.author | Ünak, P | |
dc.contributor.author | Müftüler, FZB | |
dc.contributor.author | Içhedef, ÇA | |
dc.contributor.author | Demiroglu, H | |
dc.contributor.author | Gümüser, FG | |
dc.date.accessioned | 2025-04-10T10:34:05Z | |
dc.date.available | 2025-04-10T10:34:05Z | |
dc.description.abstract | The metabolic comparison of bleomycin (BLM) and bleomycin-glucuronide (BLMG) radiolabeled with Tc-99m (Tc-99m-BLM and Tc-99m-BLMG, respectively) has been investigated in this study. Quality control procedures were carried out using thin-layer radiochromatography and high-performance liquid chromatography. To compare the metabolic behavior of BLM and its glucuronide conjugate radiolabeled with Tc-99m, scintigraphic, and biodistributional techniques were applied using male New Zealand rabbits and Albino Wistar rats. The results obtained have shown that these compounds were successfully radiolabeled with a labeling yield of about 100%. Maximum uptakes of Tc-99m-BLM and Tc-99m-BLMG metabolized as N-glucuronide were observed within 2 hours in the liver, the bladder, and the spinal cord for Tc-99m-BLM and the lung, the liver, the kidney, the large intestine, and the spinal cord for Tc-99m-BLMG, respectively. Scintigraphy and biodistributional studies performed on the experimental animals have shown that radiopharmaceutical potentials of these compounds are completely different. At the same time, uptake of the Tc-99m-BLMG was found to be better than that of Tc-99m-BLM. | |
dc.identifier.issn | 1084-9785 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14701/40274 | |
dc.language.iso | English | |
dc.title | Metabolic Comparison of Radiolabeled Bleomycin and Bleomycin-Glucuronide Labeled with 99mTc | |
dc.type | Article |