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


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-04-07

AUTHORS

Gönül Yenilmez Çiftçi, Elif Şenkuytu, Saadet Elif İncir, Esra Tanrıverdi Eçik, Yunus Zorlu, Zehra Ölçer, Yildiz Uludağ

ABSTRACT

This paper describes an amperometric method for studying DNA-drug candidate interactions. It uses an automatted electrochemical biosensor (MiSens®) 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.Graphical abstractDNA-drug interactions can be investigated by an automated biosensor device that relies on Real-time Electrochemical Profiling (REP™). More... »

PAGES

2307-2315

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00604-017-2162-y

DOI

http://dx.doi.org/10.1007/s00604-017-2162-y

DIMENSIONS

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