Radiolabeling of folate targeted multifunctional conjugate with Technetium-99m and biodistribution studies in rats
Makaleler > Tam Makale · 2012
Yazarlar: Güliz AK DEMİROZ, Fatma YURT, Şenay ŞANLIER
Journal of Drug Targeting, SCI Expanded İndekslerine Giren Dergi, Uluslararası, Wos, 2012, cilt 20, ss 509-514
DOI: 10.3109/1061186x.2012.686038
Özet
Despite the progress in the diagnosis and management of early stage disease, the management of advanced prostate cancer remains an important problem. Prostate tissue expresses folate receptor (FR) which binds both folic acid and folate-linked drugs or imaging agents. Doxorubicin is the best known and most widely used member of the anthracycline antibiotic group of anticancer agents. The aim of this work is to develop a multifunctional nanoconjugate, (99m)Tc-folate-PEG-doxorubicin, in order to investigate its radiopharmaceutical potential as a prostate cancer imaging and real-time drug location imaging agent. Through this aim, biodistribution studies of (99m)Tc-folate-PEG-doxorubicin and control groups ((99m)Tc-doxorubicin and (99m)Tc-PEG-doxorubicin) in male rats were carried out. Obtained data showed that uptake of (99m)Tc-folate-PEG-doxorubicin in prostate was significantly higher than that of the control groups due to the affinity of folate ligand to folate receptor. As a consequence, it was indicated that (99m)Tc-FOL-PEG-DOX radiolabeled conjugate which has a great target/non-target organ ratio, is specific for target organ and has a high radiopharmaceutical potential as a prostate cancer and real-time drug location imaging agent.