The study of dissolution process showed that the palladium could be dissolved at 323Kin organic system which consisted of DMSO and one of the following solvents: 1,2-dibromoethane, tribromomethane, 1,1,2,2-tetrabromoethane or tetrabromomethane. As a result of the dissolution reaction in binary organic system, the square planar palladium( II) complexes were obtained. Products of the dissolution of metallic palladium were characterized using UV-Vis and IR spectroscopy, MS spectrometry, cyclic voltammetry and analytical methods.
Due to the anticancer properties of bleomycin (BLM) complexes, production of [103Pd]bleomycin ([103Pd]BLM) was targeted. Palladium-103 (T1/2 = 16.96 d) was produced via the 103Rh(p,n)103Pd nuclear reaction using a natural rhodium target. Proton energy was 18 MeV with 200 mA irradiation for 15 h (final activity 25.9 GBq of 103Pd2+, RCP > 95%, radionuclidic purity > 99%). 103Pd was separated from the irradiated target by anion exchange using a Dowex 1´8 (Cl-)/100-200 mesh resin in the form of Pd(NH3)2Cl2 in order to react with bleomycin to yield [103Pd]BLM. Chemical purity of the final product was in accordance to the accepted limits. [103Pd]BLM was prepared with a radiochemical yield of more than 98% at 80°C in 30 min. The labeling reaction was optimized for time, temperature and ligand concentration. Radiochemical purity of more than 99% was obtained using RTLC with specific activity of about 370 MBq/mmol. The stability of the tracer was checked in the final product and presence of human serum at up to 3 h. The complex was stable in human serum at 37°C up to 2 h of incubation. Biodistribution studies using a SPECT system performed in normal rats in the first 2-3 h.
The survey reports the results achieved in carbohydrate synthesis by application of organopalladium complexes. Most remarkable results have been noted in C-glycoside synthesis and in the chemistry of unsaturated sugars. In the majority of cases high regio- and stereoselectivity of transformations is observed. Many palladium catalysts with different organic ligands have been employed. The literature up to the end of 2001 is reviewed.
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