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Noise Analysis of Ion Transfer Kinetics at the Micro Liquid/Liquid Interface
Josypčuk, Oksana ; Holub, Karel ; Mareček, Vladimír
Fluctuation analysis was utilized to determine the TEA ion transfer kinetics across the water/1,2-dichloroethane interface. The average value ks = 0.34 cm s-1 is comparable with the previously reported value ks = 0.2 cm s-1, derived from electrochemical impedance spectroscopy experiments. The experimental approach utilizing a thick wall glass microcapillary to fix the interface exhibits a very small stray capacitance value, proving this system to be suitable for determining the kinetics of the fast ion transfer across a liquid/ liquid interface. Application of a method employing a small perturbation signal prevents polarization of the inner capillary surface by current flowing through the cell. The induced polarization of the capillary can affect ion concentration at the interface due to electroosmosis and thus make the kinetics data evaluation difficult or erroneous.
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(Strept)avidin-biotin interactions at amalgam electrodes covered by thiol monolayer
Josypčuk, Bohdan ; Mareček, Vladimír ; Yosypchuk, O.
Carboxylic group of 11-mercaptoundecanoic acid (MUA) can be used to creat a peptide bond with species containing amino group, e.g., peptides, and proteins. By the help of EDC-NHS technology, streptavidin or avidin was covalently bonded with MUA-monolayer at a silver solid amalgam electrode. Such prepared electrode was used for detecting biotin and biotinylated albumin in the supporting electrolyte (0.15 M NaCl, 0.05 M TRIS, pH 7.0). Electrochemical impendance spectroscopy was performed for the biosensor response monitored by impedance spectroscopy. Binding of biotin or biotinylated albumin with (strept)avidin a change in the resistance of the sensor in the concentration range of 0.5-20 μg mL-1. Electrochemical regeneration of the amalgam electrode permits simply to renew its surface and to create the new biosensor.
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Transport of divalent cations across the gel supported phospholipid membranes
Navrátil, Tomáš ; Šestáková, Ivana ; Mareček, Vladimír
This contribution deals with elucidation of principles of transporting processes of heavy metals (mainly lead, cadmium) across the biological membranes. The real membranes were for purposes of described experiments, replaced by model membranes, which were composed of phospholipid bilayers. Two different phorpholipids (1,2-dipalmitoyl-sn-glycero-3-phosphocholine and the mixture of phospholipids obtained from soybeans (under commercial name Asolectin)) were used as the building elements for the formation of these membranes on the surface of the constructed gel electrode. The registered transporting processes have been characterized using voltammetry, and electrochemical impendance spectrometry (EIS). The impact of some parameters on these systems and processes was investigated.
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Polycrystalline gold electrode modified by thiols
Šustrová, Barbora ; Mareček, Vladimír ; Štulík, K.
The article reports on our continued investigation of modification of the gold electrode surface by thiolated compounds aimed at construction of an ion-selective sensor. Our previous work was focused on utilization of calix[4]arene molecules as a cavity sized ligand molecule. In this paper, calixarene and linear undecanethiol molecules were used as modifiers. We compared two ways of deposition thiol molecules, namely the spontaneous self-assembly process and the electrochemical deposition, in which the potential was applied on the electrode immersed into an adsorption solution. The concentration, time and potential conditions were optimized from the point of view of the SAM homogeneity. The modifying layers of calixarene and undecanthiol molecules were visualized by atomic force microscopy.
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