Optimization and Evaluation of Al18F Labeling Using a NOTA—or RESCA1-Conjugated AE105 Peptide Antagonist of uPAR

Fluorine-18 displays almost ideal decay properties for positron emission tomography (PET) and allows for large scale production. As such, simplified methods to radiolabel peptides with fluorine-18 are highly warranted. Chelation of aluminium fluoride-18 toward specific peptides represents one method to achieve this. With the current methods, chelation of aluminium fluoride-18 can be achieved using NOTA-conjugated peptides. However, the heating to 90–100◦C that is required for this chelation approach may be deleterious to the targeting moiety of the probe. Recently, a new chelator, RESCA1, was developed allowing Al18F chelation at room temperature. Here, we optimize the labeling procedure enabling high chelation efficacy of fluoride-18 at 22◦C, even at full batch labeling. The optimized procedure was tested by Al18F-labeling of RESCA1-AE105—a uPAR targeting peptide. NOTA-AE105 was also labeled with Al18F, and the two peptides were compared head-to-head. [18F]AlF-NOTA-AE105 and [18F]AlF-RESCA1-AE105 could be produced in equal radiochemical yields (RCY), radiochemical purities (RCP) and molar activities. Additionally, the two peptides showed comparable binding affinity to uPAR and uptake in cells expressing the uPAR, when evaluated in vitro. Overall, we found that the performances of [18F]AlF-NOTA-AE105 and [18F]AlF-RESCA1-AE105 were grossly comparable, but importantly RESCA1 can be labeled with aluminium fluoride-18 at 22◦C. Consequently, this study showed that RESCA1 is superior to NOTA with respect to Al18F chelation of temperature sensitive molecules, such as thermolabile peptides and proteins as well as that full batch chelation of RESCA1 with fluoride-18 is possible.

Structure and electrochemical activity of nickel aluminium fluoride nanosheets during urea electro-oxidation in an alkaline solution

An electrocatalyst of potassium nickel aluminium hexafluoride (KNiAlF6) nanosheets for enhanced urea oxidation reaction.

Investigation of the process of fluoride ions adsorption by natural sorbents

A detailed analysis of literature sources on the content of fluorides in the environment, methods of conditioning and defluoridation of water was held. The mechanism of interaction of fluorides with zeolite in the process of adsorption treatment of wastewaters and domestic waters was clarified. It was first established that in the process of adsorption there is the formation of magnesium fluoride compounds due to the binding of cations extracted from the zeolite by the mechanism of ion exchange. The mechanism of chemisorption of fluoride ions by the formation of insoluble CaF2 was also proved. According to the results of experimental research, a technological scheme has been developed, which provides the preliminary treatment of fluoride ions in the form of complexes with aluminium. In order to prevent the permeation of aluminium fluoride into the treated water, a stage of adsorption water purification was proposed. Calculations of the amount of reagent necessary to ensure the required degree of purification of water from fluoride ions were done. The statistical parameters of the process and the significance of the obtained results were calculated. The coefficient of determination of experimental data was 0.87… 0.99, the standard deviation was 0.017… 0.026.

Nb-doped variants of high surface aluminium fluoride: a very strong bi-acidic solid catalyst

Novel aluminium Nb-doped fluoride catalysts were synthesized using an aluminium hydroxide precursor to afford solids where very strong Lewis acid sites coexist with Brønsted acid sites.