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A novel dual-modality imaging agent targeting folate receptor of tumor for molecular imaging and fluorescence-guided surgery.

AbstractOBJECTIVE:
Folate receptor (FR) is an ideal target for cancer imaging because it is frequently overexpressed in major types of human tumor, whereas its expression in normal organs is highly limited. Combining nuclear and fluorescence-imaging techniques provides a novel approach for cancer imaging and monitoring the surgery. The objective of this study was to report the synthesis and characteristics of a dual-modality imaging agent, Tc-99m Folate-Gly-His-Glu-Gly-Glu-Cys-Gly-Lys(-5-carboxy-X-rhodamine)-NH2 (Folate-ECG-ROX), and verify its feasibility as both molecular imaging agent and intra-operative guidance.
METHODS:
Folate-ECG-ROX was synthesized using Fmoc solid-phase peptide synthesis. Radiolabeling of Folate-ECG-ROX with Tc-99m was done using ligand exchange via tartrate. Binding affinity and in vitro cellular uptake studies were performed. Gamma camera imaging, biodistribution and ex vivo imaging studies were performed using KB and HT-1080 tumor-bearing murine models. Tumor tissue slides were prepared and analyzed with immunohistochemistry staining and confocal microscopy. Surgical removal of tumor nodules in murine models with peritoneal carcinomatosis was performed under the fluorescence-imaging system.
RESULTS:
After radiolabeling procedures with Tc-99m, Tc-99m Folate-ECG-ROX complexes were prepared in high yield (> 97%). The binding affinity value (Kd) of Tc-99m Folate-ECG-ROX for KB cells was estimated to be 6.9 ± 0.9 nM. In gamma camera imaging, tumor to normal muscle uptake ratio of Tc-99m Folate-ECG-ROX increased with time (3.4 ± 0.4, 4.4 ± 0.7, and 6.6 ± 0.8 at 1, 2, and 3 h, respectively). In biodistribution study, %IA/g for KB tumor was 2.50 ± 0.80 and 4.08 ± 1.16 at 1 and 3 h, respectively. Confocal microscopy with immunohistochemistry staining detected strong Tc-99m Folate-ECG-ROX fluorescence within KB tumor tissue which is correlating with the fluorescent activity of anti-FR antibody. Under real-time optical imaging, the removal of visible nodules was successfully performed.
CONCLUSIONS:
In vivo and in vitro studies revealed substantial and specific uptake of Tc-99m Folate-ECG-ROX in FR-positive tumors. Thus, Tc-99m Folate-ECG-ROX could provide both pre-operative molecular imaging and fluorescence image-guidance for tumor.
AuthorsMyoung Hyoun Kim, Seul-Gi Kim, Dae-Weung Kim
JournalAnnals of nuclear medicine (Ann Nucl Med) Vol. 33 Issue 8 Pg. 606-616 (Aug 2019) ISSN: 1864-6433 [Electronic] Japan
PMID31134434 (Publication Type: Journal Article)
Chemical References
  • Folate Receptors, GPI-Anchored
  • Organotechnetium Compounds
  • Folic Acid
Topics
  • Animals
  • Biological Transport
  • Cell Transformation, Neoplastic
  • Feasibility Studies
  • Female
  • Folate Receptors, GPI-Anchored (metabolism)
  • Folic Acid (chemistry, metabolism, pharmacokinetics)
  • Humans
  • Isotope Labeling
  • KB Cells
  • Mice
  • Optical Imaging (methods)
  • Organotechnetium Compounds (chemistry)
  • Peritoneal Neoplasms (diagnostic imaging, surgery)
  • Surgery, Computer-Assisted
  • Tissue Distribution

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