Surface ligand-regulated renal clearance of MRI/SPECT dual-modality nanoprobes for tumor imaging

J Nanobiotechnology. 2024 May 13;22(1):245. doi: 10.1186/s12951-024-02516-2.

Abstract

Background: The general sluggish clearance kinetics of functional inorganic nanoparticles tend to raise potential biosafety concerns for in vivo applications. Renal clearance is a possible elimination pathway for functional inorganic nanoparticles delivered through intravenous injection, but largely depending on the surface physical chemical properties of a given particle apart from its size and shape.

Results: In this study, three small-molecule ligands that bear a diphosphonate (DP) group, but different terminal groups on the other side, i.e., anionic, cationic, and zwitterionic groups, were synthesized and used to modify ultrasmall Fe3O4 nanoparticles for evaluating the surface structure-dependent renal clearance behaviors. Systematic studies suggested that the variation of the surface ligands did not significantly increase the hydrodynamic diameter of ultrasmall Fe3O4 nanoparticles, nor influence their magnetic resonance imaging (MRI) contrast enhancement effects. Among the three particle samples, Fe3O4 nanoparticle coated with zwitterionic ligands, i.e., Fe3O4@DMSA, exhibited optimal renal clearance efficiency and reduced reticuloendothelial uptake. Therefore, this sample was further labeled with 99mTc through the DP moieties to achieve a renal-clearable MRI/single-photon emission computed tomography (SPECT) dual-modality imaging nanoprobe. The resulting nanoprobe showed satisfactory imaging capacities in a 4T1 xenograft tumor mouse model. Furthermore, the biocompatibility of Fe3O4@DMSA was evaluated both in vitro and in vivo through safety assessment experiments.

Conclusions: We believe that the current investigations offer a simple and effective strategy for constructing renal-clearable nanoparticles for precise disease diagnosis.

Keywords: Dual-modality imaging nanoprobe; Fe3O4 nanoparticles; Renal clearance; Zwitterionic ligand.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Contrast Media / chemistry
  • Female
  • Humans
  • Kidney* / diagnostic imaging
  • Kidney* / metabolism
  • Ligands
  • Magnetic Resonance Imaging* / methods
  • Magnetite Nanoparticles / chemistry
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / chemistry
  • Neoplasms / diagnostic imaging
  • Tissue Distribution
  • Tomography, Emission-Computed, Single-Photon* / methods

Substances

  • Ligands
  • Contrast Media
  • Magnetite Nanoparticles