Characterization of paraben substituted cyclotriphosphazenes, and a DNA interaction study with a real-time electrochemical profiling based biosensor

Ciftci G. Y., Senkuytu E., Incir S. E., Ecik E. T., Zorlu Y., Olcer Z., ...More

Microchimica Acta, vol.184, no.7, pp.2307-2315, 2017 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 184 Issue: 7
  • Publication Date: 2017
  • Doi Number: 10.1007/s00604-017-2162-y
  • Journal Name: Microchimica Acta
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.2307-2315
  • Keywords: Microfluidics, Anticancer agent, Cyclotriphosphazene, Biosensor, DNA-drug interaction, Gold nanoparticles, Genotoxicity, GOLD NANOPARTICLE, QUANTUM DOTS, DAMAGE, CYCLOPHOSPHAZENES, AMPLIFICATION, PHOSPHAZENES, SERUM
  • Ataturk University Affiliated: No


This paper describes an amperometric method for studying DNA-drug candidate interactions. It uses an automatted electrochemical biosensor (MiSensA (R)) based on real-time electrochemical profiling and gold nanoparticles. A biochip was prepared from a 10 x 20 mm silicon dioxide wafer. The biochip surface is modified with a self-assembled monolayer and integrated into the microfluidic system. All the steps of the DNA-drug interaction assay have been performed during fluid flow. Biotinylated surface DNA has been captured on a NeutrAvidin -modified biochip surface. Hybridization of the complementary target sequence and biotinylated detection probe to the surface DNA strand was studied with and without the addition of newly synthesised drug candidates. NeutrAvidin and enzyme modified gold nanoparticles were then injected to bind to the biochip surface. The real-time reading of the amperometric response during the substrate injection results in the biosensor signal. The DNA interaction analysis was exemplarily applied to test the activity of paraben-substituted cyclotriphosphazenes as potential anticancer agents. Two of the synthesised compounds were identified that are capable of inducing DNA damage by 27 and 34%, respectively.