Pharmaceuticals (Nov 2019)

New <sup>55</sup>Co-labeled Albumin-Binding Folate Derivatives as Potential PET Agents for Folate Receptor Imaging

  • Lauren L. Radford,
  • Solana Fernandez,
  • Rebecca Beacham,
  • Retta El Sayed,
  • Renata Farkas,
  • Martina Benešová,
  • Cristina Müller,
  • Suzanne E. Lapi

DOI
https://doi.org/10.3390/ph12040166
Journal volume & issue
Vol. 12, no. 4
p. 166

Abstract

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Overexpression of folate receptors (FRs) on different tumor types (e.g., ovarian, lung) make FRs attractive in vivo targets for directed diagnostic/therapeutic agents. Currently, no diagnostic agent suitable for positron emission tomography (PET) has been adopted for clinical FR imaging. In this work, two 55Co-labeled albumin-binding folate derivatives-[55Co]Co-cm10 and [55Co]Co-rf42-with characteristics suitable for PET imaging have been developed and evaluated. High radiochemical yields (≥95%) and in vitro stabilities (≥93%) were achieved for both compounds, and cell assays demonstrated FR-mediated uptake. Both 55Co-labeled folate conjugates demonstrated high tumor uptake of 17% injected activity per gram of tissue (IA/g) at 4 h in biodistribution studies performed in KB tumor-bearing mice. Renal uptake was similar to other albumin-binding folate derivatives, and liver uptake was lower than that of previously reported [64Cu]Cu-rf42. Small animal PET/CT images confirmed the biodistribution results and showed the clear delineation of FR-expressing tumors.

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