Synthesis, Characterization, and Magnetic Properties of Fe(BIP)3, a Novel Paramagnetic Relaxation Agent
<b>Background/Objectives</b>: First row transition metal ions have recently regained attention in coordination chemistry as alternatives to gadolinium-based paramagnetic contrast agents, motivated by emerging safety concerns associated with certain Gd<sup>3+</sup>-based contrast agents. In this study, we report the development of a novel homoleptic diketonate Fe<sup>3+</sup> complex functionalized with biocompatible indole moieties. We investigate its potential as a paramagnetic relaxation agent by evaluating its ability to modulate the T<sub>1</sub> and T<sub>2</sub> relaxation times of water proton. <b>Methods</b>: Iron(III) tris-1,3-(1-methylindol-3-yl)propanedionate [Fe(BIP)<sub>3</sub>] was synthesized via a thermal method from bis(1-methylindol-3-yl)-1,3-propanedione (HBIP) using Fe(ClO<sub>4</sub>)<sub>3</sub>∙6 H<sub>2</sub>O as the metal source. The complex was characterized by UV-Vis, IR and NMR spectroscopy, differential scanning calorimetry-thermogravimetric analysis, and single-crystal X-ray diffraction. Fe(BIP)<sub>3</sub> aggregation behavior in aqueous environment, including size and morphology of aggregates, was investigated using dynamic light scattering and scanning electron microscopy. Incorporation of the aggregates into phospholipid vesicles was evaluated by fluorescence resonance energy transfer and fluorescence correlation spectroscopy. The paramagnetic properties of monomeric Fe(BIP)<sub>3</sub> were probed in solution by nuclear magnetic resonance recurring to the Evans bulk magnetization method. <b>Results</b>: The designed synthetic procedure successfully afforded Fe(BIP)<sub>3</sub>, which was fully characterized by UV-Vis and IR spectroscopy, as well as single-crystal X-ray diffraction. Aqueous solutions of Fe(BIP)<sub>3</sub> spontaneously formed rice-grain-shaped nanoscale aggregates of hydrodynamic radius ≈ 30 nm. Incorporation of these aggregates into phospholipid vesicles enhanced their stability. The longitudinal r<sub>1</sub> and transverse r<sub>2</sub> relaxivities of Fe(BIP)<sub>3</sub> aggregates were assessed to be 1.92 and 52.3 mM<sup>-1</sup>s<sup>-1</sup>, respectively, revealing their potential as paramagnetic relaxation agents. <b>Conclusions</b>: Fe(BIP)<sub>3</sub> aggregates, stabilized through incorporation into phospholipid vesicles, demonstrate promising potential as novel paramagnetic relaxation agents in aqueous environments.
Authors
- Sandro Recchia
- Benedict Josua Elvers
- Matteo Uboldi
- Federico Vavassori
- Veronica Pettinato
- Marco Lamperti
- Mauro Fasano
- Roberto Tallarita
- Luca Nardo
- Giosuè Saibene
- Pietro Anzini
- Carola Schulzke
- Andrea Penoni
- Angelo Maspero
- Veronica Remori
Institutions
- University of Insubria (IT)
- Universität Greifswald (DE)
- Instituto de Óptica "Daza de Valdés" (ES)
Publication Details
- Journal
- Pharmaceuticals
- Published
- 2026-01-27
- DOI
- https://doi.org/10.3390/ph19020221
- Primary Topic
- Lanthanide and Transition Metal Complexes
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Università degli Studi dell'Insubria