Author/Authors :
Janrungroatsakul، نويسنده , , Wanwisa and Vilaivan، نويسنده , , Tirayut and Vilaivan، نويسنده , , Chotima and Watchasit، نويسنده , , Sarayut and Suksai، نويسنده , , Chomchai and Ngeontae، نويسنده , , Wittaya and Aeungmaitrepirom، نويسنده , , Wanlapa and Tuntulani، نويسنده , , Thawatchai، نويسنده ,
Abstract :
Four calix[4]arene derivatives containing various donor atoms and different topology (L1−L4) have been synthesized and used as neutral ionophores to fabricate silver ion selective electrodes (Ag-ISEs) which were characterized in terms of their potentiometric selectivities and complex formation constants. The ionophore L2 having two nitrogen and two sulfur donors showed stronger interactions with Ag+ and the highest selectivity coefficient towards Ag+. The best membrane electrode was prepared from L2 and used to fabricate silver ion selective microelectrodes (Ag-ISμEs) which could detect silver ions in 1000 μL samples with detection limit around 1 μM using sodium ion microelectrodes as a pseudo reference electrode. Such potentiometric measurement was then applied to detect DNA hybridization on a gold substrate, employing immobilized lipoic acid-modified pyrrolidinyl PNA (Lip-acpcPNA) as a probe. The hybridization between the neutral Lip-acpcPNA probe and DNA target led to a negatively charged surface that could bind positively charged silver nanoparticles (AgNPs+) via electrostatic interactions. The hybridization signal was observed by dissolution of the electrostatically adsorbed AgNPs+ with hydrogen peroxide. Excellent discrimination of complementary from single mismatched and non-complementary DNA targets was achieved under non-stringent conditions. The detection limit of DNA was 0.2 μM in 1000 μL samples.
Keywords :
peptide nucleic acid , Silver ion selective electrode , DNA hybridization , Silver nanoparticles