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In this article, we present the synthesis and characterization of new acyclic pyridine-containing polyaminocarboxylate ligands H4aPyta and H6aPyha, which differ in structural rigidity and the number of chelating groups. Their abilities to form complexes with Cu2+, Ga3+, Y3+, and Bi3+ cations, as well as the stability of the complexes, were evaluated by potentiometric titration method, radiolabeling with the corresponding radionuclides, in vitro studies, mass spectrometry, and HPLC. The structures of the resulting complexes were determined using NMR spectroscopy and DFT calculations. The results obtained made it possible to evaluate the influence of the structural features of the complexes on their stability. The developed chelators H4aPyta and H6aPyha were proved to be promising for further research in the field of radiopharmaceuticals. [ABSTRACT FROM AUTHOR]

Formation of Sc radioisotopes under the irradiation of titanium of natural isotopic composition by bremsstrahlung photons with energies up to 55 MeV was studied. The yield of 47Sc is 5·105 Bq/μA h (g/cm2). Inevitable impurities are 46Sc and 48Sc (1.5% and 9.1% of 47Sc radioactivity at EOB, respectively). 47Sc was separated by extraction chromatography on a DGA resin in HNO3 and HCl media. The separation procedure takes about 2 h, the radiochemical efficiency was > 97%. The result was compared with other photonuclear experiments on titanium nuclei. It is shown that the photonuclear method can be used for the production of therapeutic amounts of 47Sc. [ABSTRACT FROM AUTHOR]

Production of medical radionuclide 67Cu by the irradiation of Zn of natural isotopic composition by bremsstrahlung photons of maximum energy of 55 MeV was studied. Production yields of 67Cu and other activation products were determined. The yield of 67Cu is (2.34 ± 0.07) × 105 Bq/(μA h g/cm2) at EOB. The experimental data were compared with the results of other experiments and theoretical calculations based on the statistical model in the TALYS software and on the combined model of photonuclear reactions. Technique of chemical separation of 67Cu from irradiated zinc target based on extraction chromatography using CU Resin was applied. Radiochemical yield was > 95%, separation time was 1 h. The possibility of production of medical quantities was discussed. [ABSTRACT FROM AUTHOR]

In this work, the separation of 89Zr, a radionuclide promising for positron-emission tomography, from an irradiated yttrium target using different extraction-chromatographic resins (TEVA, UTEVA, TRU, and LN resins ©Triskem) was studied. Distribution coefficients of Zr(IV) onto TEVA, LN (in HCl solutions), and onto TRU (in HCl and HNO3) were determined. The optimum conditions for the separation of Zr(IV) and Y(III) using these resins were proposed. In each case, the maximum separation factor was higher than 105. The developed separation procedures allow to obtain 89Zr of high radiochemical purity for dilute mineral acids. [ABSTRACT FROM AUTHOR]

A method for obtaining 156, 155, 154m2, 154, 153Tb radiotracers by the irradiation of a europium oxide target of natural isotopic composition by 27 MeV α-particles is proposed. Terbium can be efficiently separated from bulk of europium by the reduction of the latter by zinc in an acidic solution and precipitation as EuSO4. The optimum Zn/Eu3+ and (NH4)2SO4/Eu3+ molar ratios are 20 and 3, respectively. Terbium is additionally purified from europium and gadolinium by extraction chromatography using LN Resin. It is demonstrated that optimum separation is attained in 0.6 M HNO3. The Tb/Eu separation coefficient was ~5 · 105. The yield of terbium was about 90 %. Time of all steps was 1.5-2 h. The proposed procedure makes it possible to obtain no carrier added terbium radiotracers. [ABSTRACT FROM AUTHOR]

In this article, we present the synthesis and characterization of new acyclic pyridine-containing polyaminocarboxylate ligands H4aPyta and H6aPyha, which differ in structural rigidity and the number of chelating groups. Their abilities to form complexes with Cu2+, Ga3+, Y3+, and Bi3+ cations, as well as the stability of the complexes, were evaluated by potentiometric titration method, radiolabeling with the corresponding radionuclides, in vitro studies, mass spectrometry, and HPLC. The structures of the resulting complexes were determined using NMR spectroscopy and DFT calculations. The results obtained made it possible to evaluate the influence of the structural features of the complexes on their stability. The developed chelators H4aPyta and H6aPyha were proved to be promising for further research in the field of radiopharmaceuticals. [ABSTRACT FROM AUTHOR]

In this article, we present the synthesis and characterization of new acyclic pyridine-containing polyaminocarboxylate ligands H4aPyta and H6aPyha, which differ in structural rigidity and the number of chelating groups. Their abilities to form complexes with Cu 2+ , Ga 3+ , Y 3+ , and Bi 3+ cations, as well as the stability of the complexes, were evaluated by potentiometric titration method, radiolabeling with the corresponding radionuclides, in vitro studies, mass spectrometry, and HPLC. The structures of the resulting complexes were determined using NMR spectroscopy and DFT calculations. The results obtained made it possible to evaluate the influence of the structural features of the complexes on their stability. The developed chelators H4aPyta and H6aPyha were proved to be promising for further research in the field of radiopharmaceuticals.