Fluorescein-Tagged 1Methyl-o-carborane A Promising Agent for Boron Neutron Capture Therapy

Introduction

Key Findings from the Study

  • Novel Synthesis Approach: Researchers conjugated fluorescein with 1-methyl-o-carborane through a Williamson ether synthesis reaction.
  • Improved Boron Delivery: The new conjugate offers higher boron content compared to existing clinical agents BSH and BPA.
  • Biological Evaluation:
    • In squamous cell carcinoma (SCC-VII), the conjugate showed moderate cytotoxicity (IC50 ≈ 1 mM), making it less toxic than traditional agents.
    • In pancreatic cancer cells (MIA PaCa-2), flow cytometry and fluorescent imaging confirmed efficient uptake and uniform intracellular distribution.
  • Potential Theranostic Use: Fluorescein labeling enabled real-time tracking under fluorescence microscopy, highlighting diagnostic and therapeutic potential.

Broader Context in BNCT Research

Related Resources

Conclusion and Future Directions

The fluorescein-tagged 1-methyl-o-carborane conjugate represents a promising theranostic candidate for BNCT. Its high boron content, moderate cytotoxicity, and efficient uptake in cancer cells warrant further clinical evaluation. Upcoming BNCT trials will determine its potential role as a next-generation delivery agent for targeted cancer therapy.

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