AI Article Synopsis

  • Multinuclear tungsten complexes are being explored as potential new contrast agents for improving CT imaging diagnostics due to their high tungsten content and low osmolality.
  • A ligand strategy involving amino acids and EDTA derivatives was used to synthesize stable tungsten complexes, which were thoroughly characterized using various scientific techniques.
  • While some complexes showed good stability and lower osmolality, they lacked sufficient water solubility for use in medical imaging, but adjustments to the ligand structure could enhance their solubility.

Article Abstract

Multinuclear tungsten complexes are intriguing candidates for new contrast media that can provide substantial improvements in CT imaging diagnostics. Herein, we present a ligand strategy, based on amino acids, and mono- and disubstituted EDTA derivatives, that enables the development of stable complexes with high tungsten content and reasonably low osmolality. Accordingly, a series of neutral and monoanionic di-μ-sulfido W(V) dimers have been synthesized a convenient procedure utilizing microwave heating in combination with ion-pair HPLC reaction monitoring. The compounds were characterized in detail by various techniques, including ESI-HRMS, NMR spectroscopy, HPLC, elemental analysis, and X-ray crystallography. The aqueous stability of the complexes under physiologically relevant conditions, and during heat sterilization was also examined as an initial assessment of their potential applicability as radiocontrast agents. Monoanionic complexes featuring monosubstituted EDTA derivatives have demonstrated high stability, while producing a lower number of ions in solution (resulting in lower osmolality) in comparison to their bis-anionic EDTA counterparts. Nevertheless, they exhibited insufficient water solubility for application as intravascular contrast agents. However, our study showed that aqueous solubility of this type of complexes can be tuned by small modifications in the ligand structure.

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Source
http://dx.doi.org/10.1039/d2dt01470jDOI Listing

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