Preparation and first biological evaluation of novel Re-188/Tc-99m peptide conjugates with substance-P

Appl Radiat Isot. 2014 Sep:92:25-31. doi: 10.1016/j.apradiso.2014.06.003. Epub 2014 Jun 12.

Abstract

Introduction: New (188)Re and (99m)Tc peptide conjugates with substance- P (SP) were prepared and biologically evaluated. The radiopharmaceuticals have been labelled with the [M≡N](2+) (M=(99m)Tc, (188)Re) core using a combination of π-donor tridentate and π-acceptor monodentate ancillary ligands.

Methods: The new radiopharmaceuticals have been prepared through a two-step reaction by simultaneous addition of the tridentate and monodentate ligands to a vial containing a preformed [M≡N](2+) core. The tridentate ligand was formed by linking two cysteine residues to the terminal arginine of the undecapeptide SP, whereas the monodentate ligand was a tertiary phosphine. The preparation of the corresponding Re-188 derivative required developing a more complex chemical procedure to obtain the [Re≡N](2+) core in satisfactory yields. Characterization of the resulting products was obtained by chromatographic methods. Biological evaluation was performed for both Tc-99m and Re-188 derivatives by in-vitro studies on isolated cells expressing NK1-receptors. In-vivo imaging in mice was carried out using a small-animal YAP(S)PET tomograph.

Conclusion: New Tc-99m and Re-188 peptide radiopharmaceuticals with SP have been prepared in high-yield and with high-specific activity. Both Tc-99m and Re-188 peptide radioconjugates exhibit high affinity for NK1 receptors, thus giving further evidence to the empirical rule that structurally related Tc-99m and Re-188 radiopharmaceuticals exhibit identical biological properties.

Keywords: Metal nitrido radiopharmaceuticals; Peptide radiopharmaceuticals; Rhenium-188; Substance-P; Technetium-99m.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Drug Stability
  • Isotope Labeling / methods
  • Metabolic Clearance Rate
  • Mice
  • Neoplasms, Experimental / diagnostic imaging
  • Neoplasms, Experimental / metabolism*
  • Organ Specificity
  • Radioisotopes / chemistry
  • Radioisotopes / pharmacokinetics*
  • Radiopharmaceuticals / chemical synthesis
  • Radiopharmaceuticals / pharmacokinetics
  • Rats
  • Rhenium / chemistry*
  • Rhenium / pharmacokinetics*
  • Substance P / chemistry
  • Substance P / pharmacokinetics*
  • Technetium / chemistry*
  • Technetium / pharmacokinetics*
  • Tissue Distribution
  • Tomography, Emission-Computed, Single-Photon / methods

Substances

  • Radioisotopes
  • Radiopharmaceuticals
  • Substance P
  • Rhenium
  • Technetium