Promising Performance of 4HMS, a New Zirconium-89 Octadendate Chelator

摘要

Over the last decade, the interest in zirconium-89 (~(89)Zr) as a positron-emitting radionuclide increased considerably because of its standardized production and its physical half-life (78.41 h), which matches the biological half-life of antibodies and its successful use in preclinical and clinical applications. So far, desferrioxamine (DFO), a commercially available chelator, has been mainly used as a bifunctional chelating system. However, there are some concerns regarding the in vivo stability of the [~(89)Zr]Zr-DFO complex. In this study, we report the synthesis of an acyclic N -hydroxy-N -methyl succinamide-based chelator (4HMS) with 8 coordination sites and our first investigations into the use of this new chelator for ~(89)Zr complexation. In vitro and in vivo comparative studies with [~(89)Zr]Zr-4HMS and [~(89)Zr]Zr-DFO are presented. The 4HMS chelator was synthesized in four steps starting with an excellent overall yield. Both chelators were quantitatively labeled with ~(89)Zr within 5–10 min at pH 7 and room temperature; the molar activity of [~(89)Zr]Zr-4HMS exceeded (>3 times) that of [~(89)Zr]Zr-DFO. [~(89)Zr]Zr-4HMS remained stable against transmetalation and transchelation and cleared from most tissues within 24 h. The kidney, liver, bone, and spleen uptakes were significantly low for this ~(89)Zr-complex. Positron emission tomography images were in accordance with the results of the biodistribution in healthy mice. Based on DFT calculations, a rationale is provided for the high stability of ~(89)Zr-4HMS. This makes 4HMS a promising chelator for future development of ~(89)Zr-radiopharmaceuticals.