Search Results (6)

Background: The ⁸⁹Zr radioisotope is increasingly vital in positron emission tomography (PET), especially immuno-PET, due to its long half-life of 78.4 h, allowing extended tracking of biological processes. This makes it particularly suitable for researching medicines with slow pharmacokinetics and enhances the precision of molecular imaging, especially in oncology. Despite zirconium’s potential for skeletal accumulation, effective chelation with agents like deferoxamine (DFO) enables high-resolution imaging of antigen-specific tumours, such as HER2-positive breast cancer, offering insights into tumour biology and treatment response. Methods: ⁸⁹Zr was produced at the ACSI TR-19 cyclotron via ⁸⁹Y(p,n)⁸⁹Zr reaction. Natural yttrium foils (250 μm) were irradiated with 12.9 MeV protons on target, with 100 μA·h. An HER2-targeting affibody was synthesized and conjugated with p-NCS-Bz-DFO (1:4 mass ratio) at 37 °C for 60 min (pH 9.2 ± 0.2), then purified on a PD-10 column. Radiolabelling was performed with [⁸⁹Zr]Zr-oxalate at pH ranging from 7.0 to 9.0, with concentrations from 110 to 460 MBq/mL. Results: Final activity reached 2.95 ± 0.31 GBq/batch (EOB corrected), with ≥ 99.9% radionuclide and ≥95% radiochemical purities. The anti-HER2 affibody was successfully radiolabelled with ⁸⁹Zr, resulting in a radiochemical purity of over 85% with molar activity of 26.5 ± 4.4 and 11.45 MBq/nmol at pH 7.0–7.5. In vitro tests on BT-474 and MCF-7 cell lines confirmed high uptake in HER2-positive cells, validating specificity and stability. Conclusions: The successful synthesis and labelling of the [⁸⁹Zr]Zr-p-NCS-Bz-DFO-anti-HER2 affibody are promising achievements for its further application in targeted immuno-PET imaging for HER2-positive malignancies. Further in vivo studies are needed to support its clinical translation. Full article

A study of the morphology and evolution of the microstructure during thermal decomposition of Y₂(C₂O₄)₃·10H₂O was conducted, and the stages and factors having the greatest impact on particle size and specific surface area were identified. The effect of the yttrium oxalate hexahydrate phases on the course of decomposition was also investigated. The evolution of the morphology and microstructure of decomposition products was explained from the analysis of volume shrinkage at various stages of the reaction. The formation of oxycarbonate is accompanied by the largest shrinkage during the reaction. At this stage, there is a significant increase in the specific surface area to 60–90 m²/g. Conversely, the morphology and microstructure of the particles during the transformation of oxycarbonate into yttrium oxide change insignificantly. Yttrium oxide powders obtained from the monoclinic and triclinic hexahydrate phases have the same specific surface area, but different morphology and bulk density due to pseudomorph formation. The carbon formed during thermolysis was shown to affect the specific surface area of the decomposition product. Two methods for producing yttrium oxide with high specific surface area have been proposed, and nanocrystalline yttrium oxide with a specific surface area of 65 m²/g was obtained. Full article

Background: Endocorporeal laser lithotripsy (EL) during flexible ureteroscopy (URS-f) often uses “dusting” settings with “painting” technique. The displacement velocity of the laser fiber (LF) at the stone surface remains unknown and could improve EL’s ablation rates. This in vitro study aimed to define the optimal displacement velocity (ODV) for both holmium:yttrium-aluminium-garnet (Ho:YAG) and thulium fiber laser (Tm-Fiber). Methods: A 50W-TFL (IRE Polus^®, Moscow, Russia) and a 30W-MH1-Ho:YAG laser (Rocamed^®, Signes, Provence-Alpes-Côte d’Azur, France), were used with 272 µm-Core-Diameter LF (Sureflex, Boston Scientific^©, San Jose, CA, USA), comparing three TFL modes, “fine dusting” (FD: 0.05–0.15 J/100–600 Hz); “dusting” (D: 0.5 J/30–60 Hz); “fragmentation” (Fr: 1 J/15–30 Hz) and two Ho:YAG modes (D: 0.5 J/20 Hz, Fr: 1 J/15 Hz). An experimental setup consisting of immerged cubes of calcium oxalate monohydrate (COM) stone phantoms (Begostone Plus, Bego^©, Lincoln, RI, USA) was used with a 2 s’ laser operation time. LF were in contact with the stones, static or with a displacement of 5, 10 or 20 mm. Experiments were repeated four times. Stones were dried and µ-scanned. Ablation volumes (mm³) were measured by 3D-segmentation. Results: ODV was higher in dusting compared to fragmentation mode during Ho:YAG lithotripsy (10 mm/s vs. 5 mm/s, respectively). With Tm-Fiber, dusting and fragmentation OVDs were similar (5 mm/s). Tm-Fiber ODV was lower than Ho:YAGs in dusting settings (5 mm/s vs. 10 mm/s, respectively). Without LF displacement, ablation volumes were at least two-fold higher with Tm-Fiber compared to Ho:YAG. Despite the LF-DV, we report a 1.5 to 5-fold higher ablation volume with Tm-Fiber compared to Ho:YAG. Conclusions: In dusting mode, the ODV^Tm-Fiber is lower compared to ODV^Ho:YAG, translating to a potential easier Tm-Fiber utilization for “painting” dusting technique. The ODV determinants remain unknown. Dynamic ablation volumes are higher to static ones, regardless of the laser source, settings or LF displacement velocity. Full article

The increased interest in ⁸⁹Zr-labelled immunoPET imaging probes for use in preclinical and clinical studies has led to a rising demand for the isotope. The highly penetrating 511 and 909 keV photons emitted by ⁸⁹Zr deliver an undesirably high radiation dose, which makes it difficult to produce large amounts manually. Additionally, there is a growing demand for Good Manufacturing Practices (GMP)-grade radionuclides for clinical applications. In this study, we have adopted the commercially available TRASIS mini AllinOne (miniAiO) automated synthesis unit to achieve efficient and reproducible batches of ⁸⁹Zr. This automated module is used for the target dissolution and separation of ⁸⁹Zr from the yttrium target material. The ⁸⁹Zr is eluted with a very small volume of oxalic acid (1.5 mL) directly over the sterile filter into the final vial. Using this sophisticated automated purification method, we obtained satisfactory amount of ⁸⁹Zr in high radionuclidic and radiochemical purities in excess of 99.99%. The specific activity of three production batches were calculated and was found to be in the range of 1351–2323 MBq/µmol. ICP-MS analysis of final solutions showed impurity levels always below 1 ppm. Full article

The separation and concentration processes of heavy rare-earth metals—yttrium, ytterbium, erbium, and dysprosium—during stripping from the organic phase based on di-2-ethylhexylphosphoric acid (D2EHPA, or DEHPA) solutions were investigated in this work. Optimal conditions providing high separation factors of rare-earth metals (REM) and their extraction degree to the aqueous phase were determined. The usage of sulfuric acid solutions with a concentration of 2–6 mol/L, depending on the type of extracted rare-earth element, was proposed as a stripping agent for rare-earth metals (REM), and the usage of oxalic acid solution was proposed as an iron stripping solution from the organic phase. To increase the REM stripping efficiency, the antagonistic effect of tributyl phosphate in the di-2-ethylhexylphosphoric acid-kerosene-tributyl phosphate system was considered. The possibility of increasing the capacity of the organic solvent by cleaning the organic phase from iron ions using oxalic acid solutions was revealed. The influence of temperature, aqueous and organic phase ratio, stirring rate, and re-extractant concentration on the distribution and separation factors of adjacent heavy rare-earth-metal (HREM) pairs during the re-extraction process were determined. A schematic diagram of the laboratory-tested separation process of heavy rare-earth metals into individual components with the obtaining of yttrium and ytterbium concentrates containing more than 99% of the target components was proposed. Full article

Waste electrical and electronic equipment (WEEE) has increased in recent decades due to the continuous advancement of technology in the modern world. These residues have various metals that are found in concentrations that make their recovery profitable. A group of metals of interest are the rare earths such as europium and yttrium, as well as semiconductors such as indium. Yttrium was recovered from cathode ray tubes that were manually dismantled. The resulted powder was leached with HNO₃, and then the solution was submitted to solvent extraction with di-(2-ethylhexyl) phosphoric acid (DEHPA) using n-heptane as a diluent. For re-extraction, HNO₃ was used again, and yttrium was precipitated by adding four times the stoichiometric amount of oxalic acid, reaching 68% yttrium purity. Indium was recovered from the liquid crystal display (LCD) screens for which the pulverized material was leached with H₂SO₄. Then, the indium sulfate was subjected to solvent extraction using DEHPA as an extractant, and diesel as a diluent. The re-extraction was carried out again with H₂SO₄, and the obtained acid solution was evaporated until the indium precipitated, reaching a recovery of 95%. The investigations that were carried out show that it is feasible to recover these metals in the form of oxides or phosphates with high commercial value. Full article