Design of the New Closo -Dodecarborate-Containing Gemcitabine Analogue for the Albumin-Based Theranostics Composition.
Valeria I RaskolupovaMeiling WangMayya Alexandrovna DymovaGleb O PetrovIvan M ShchudloSergey Yu TaskaevTatyana V AbramovaTatyana S GodovikovaVladimir N SilnikovTatyana V PopovaPublished in: Molecules (Basel, Switzerland) (2023)
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 (IC 50 ) 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.
Keyphrases
- combination therapy
- induced apoptosis
- cell cycle arrest
- locally advanced
- human serum albumin
- squamous cell carcinoma
- blood pressure
- radiation therapy
- endoplasmic reticulum stress
- fluorescence imaging
- cell death
- quantum dots
- high intensity
- mesenchymal stem cells
- bone marrow
- cell proliferation
- magnetic resonance
- body composition
- replacement therapy
- living cells
- climate change
- single molecule