Molecules (Mar 2023)

Design of the New <i>Closo</i>-Dodecarborate-Containing Gemcitabine Analogue for the Albumin-Based Theranostics Composition

  • Valeria I. Raskolupova,
  • Meiling Wang,
  • Maya A. Dymova,
  • Gleb O. Petrov,
  • Ivan M. Shchudlo,
  • Sergey Yu. Taskaev,
  • Tatyana V. Abramova,
  • Tatyana S. Godovikova,
  • Vladimir N. Silnikov,
  • Tatyana V. Popova

DOI
https://doi.org/10.3390/molecules28062672
Journal volume & issue
Vol. 28, no. 6
p. 2672

Abstract

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Combination therapy is becoming an increasingly important treatment strategy because multi-drugs can maximize therapeutic effect and overcome potential mechanisms of drug resistance. A new albumin-based theranostic containing gemcitabine closo-dodecaborate analogue has been developed for combining boron neutron capture therapy (BNCT) and chemotheraphy. An exo-heterocyclic amino group of gemcitabine was used to introduce closo-dodecaborate, and a 5′-hydroxy group was used to tether maleimide moiety through an acid-labile phosphamide linker. The N-trifluoroacylated homocysteine thiolactone was used to attach the gemcitabine analogue to human serum albumin (HSA) bearing Cy5 or Cy7 fluorescent dyes. The half-maximal inhibitory concentration (IC50) of the designed theranostic relative to T98G cells was 0.47 mM with the correlation coefficient R = 0.82. BNCT experiments resulted in a decrease in the viability of T98G cells, and the survival fraction was ≈ 0.4.

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