National Repository of Grey Literature 23 records found  1 - 10nextend  jump to record: Search took 0.01 seconds. 
Study of redox and adsorption features of bile acids on hanging mercury drop electrode
Yershova, Polina ; Schwarzová, Karolina (advisor) ; Gajdár, Július (referee)
Bile acids are the end products of cholesterol metabolism and are important biological surfactants. The curved shape of their chains allows the cyclization of molecules, and the formation of a supramolecular structure. The goal of this thesis was to study the electrochemical and adsorption behavior of selected bile acids: lithocholic, deoxycholic and cholic acids. The measurements were carried out in the medium Brittonův-Robinson buffer:methanol in the ratio 9:1 using cyclic voltammetry and AC voltammetry methods and measuring the dependence of the differential capacitance Cd on the applied potential E. A hanging mercury drop electrode was used as a working electrode. The measurements showed that bile acids are adsorbed on the surface of the electrode and organizing themselves in self assembled monolayers (SAM). In our case we have observed formation of 2D condensed layers as specific form of SAM. Transfer techniques were used to demonstrate bile acid adsorption. A study of the behavior of lithocholic acid as a function of different pH values showed that only at pH 10.0 to 12.0 2D 2D condensation occurs, i. e. that at pH values in the range of 2.0 to 9.0 it is another type of adsorption. On AC voltammograms, there are a maximum of two areas in which peaks occur: the first is around -0.2 V and the...
Voltammetric Determination of Genotoxic Nitrobiphenyls
Horáková, Eva ; Vyskočil, Vlastimil (advisor) ; Navrátil, Tomáš (referee)
The presented diploma thesis is devoted to study of determination of 4-nitrobiphenyl (4-NBP) in model river water by DC voltammetry (DCV) and differential pulse voltammetry (DPV) at m-AgSAE (diploma thesis relates to bachelor thesis, in it DCV and DPV methods for determination of 4-NBP in deionized water were developed). Limit of determination (LOD) is 2·10-7 mol·l-1 by DCV and 4·10-7 mol·l-1 by DPV. The adsorptive stripping DPV (AdSDPV) technique was tested to archive lower LOD the AdSDPV, optimal conditions were not found. Electrochemical behavior of 2-nitrobiphenyl (2-NBP) at m-AgSAE was studied. Optimal conditions for its determination by both techniques DCV and DPV were found in methanol-0,01 mol·l-1 LiOH (1:9) and in this medium peak current dependence in 1·10-7 mol·l-1 to 1·10-4 mol·l-1 2-NBP (LOD ≈ 2·10-7 mol·l-1 by DCV and 1·10-7 mol·l-1 by DPV) concentration range was measured. Developed methods were successfully tested for determination of 2-NBP in drinking and river water samples. For both mediums obtained LODs were 2·10-7 mol·l-1 by DCV and 1·10-7 mol·l-1 by DPV. AdSDPV technique was unsuccessfully tested to achieve lower LOD. Optimal conditions for simultaneous determination of 4-NBP and 2-NBP by DPV technique at m-AgSAE were found: methanol-0,25 mol·l-1 acetate buffer (pH = 6,0) 3:7....
Study of electrochemical behaviour of tauroursodeoxycholic acid at mercury-based electrodes
Pišnová, Kateřina ; Schwarzová, Karolina (advisor) ; Navrátil, Tomáš (referee)
This thesis deals with electrochemical behaviour of tauroursodeoxycholic acid (TUDCA) at silver solid amalgam electrode modified by mercury meniscus (m-AgSAE), polished silver solid amalgam electrode (p-AgSAE) and hanging mercury dropping electrode (HMDE). This thesis is a part of a bigger scientific research that deals with synthesis and characterization of supramolecular systems based on natural steroid compounds and its conjugates. TUDCA offers one reduction peak at m-AgSAE in the environment of Britton - Robinson buffer in range of pH 6.0 - 13.0. The potential of this peak is around −1200 mV. Using cyclic voltammetry was determined that the process on the electrode surface is quasireversible, the reduction is controlled by diffusion and the anodic process is controlled by adsorption. Concentration dependence measured at HMDE by direct current voltammetry in 0.04 mol∙l-1 borat buffer (pH 9.1) is linear in two concentration intervals - 1∙10-3 - 2∙10-4 mol∙l-1 and 1∙10-4 - 8∙10-6 mol∙l-1 of TUDCA. There was no linear dependence between the increase of concentration of TUDCA and the height of the peak obtained on amalgam electrodes by methods DC, DP, cyclic and "square-wave" voltammetry. On HMDE was in several short concentration intervals measured by a CV method a linear dependence of cathodic and...
The use of mercury-based electrode materials for the study of electrochemical reduction of selected bile acids
Hulová, Dagmar ; Schwarzová, Karolina (advisor) ; Navrátil, Tomáš (referee)
The electrochemic's behaviour of the bile acids (cholic, glycocholic, deoxycholic, ursodeoxycholic and lithocholic acid) was studied on the meniscus-modified silver solid amalgam electrode (m-AgSAE) by differential pulse voltammery. Bile acids provide in the solution of the Britton - Robinson buffer and methanol (9:1) in the pH range 3.0 to 12.0 a cathodal signal in the high negative potentials: cholic acid, deoxycholic acid, ursodeoxycholic acid and lithocholic acid about −1400 mV and glycocholic acid, which alone is the conjugate with glycine, about −1500 mV. Cholic acid, glycocholic acid, deoxycholic acid and ursodeoxycholic acid provide the highest peaks to pH 5.0, approximately in their pKa values. Lithocholic acid provides peaks from pH 7.0. It was demonstrated by the cyclic voltammetry that the electrochemical behavior is influenced by the adsorption of the bile acids to the electrode; presumed reaction at the working electrode - a reduction of a proton of a carboxylic group, is controlled by the diffusion and the process is quasireversible. Utilization of the electrochemical reduction of bile acids for the voltammetric determination does not seem very suitable. It has been proven that the presence of the methanol deteriorates the measuring results for glycocholic acid. In the presence of...
Electrochemical reduction of dehydrocholic and chenodeoxycholic acid at stationary mercury and amalgam electrodes
Patáková, Adéla ; Schwarzová, Karolina (advisor) ; Vyskočil, Vlastimil (referee)
This thesis deals with the study of electrochemical behaviour of dehydrocholic and chenodeoxycholic acid at stationary mercury-based electrodes - hanging mercury dropping electrode and silver solid amalgam electrode modified by a mercury meniscus. This is the first study of electrochemical behaviour of dehydrocholic acid which offers tree peaks with potentials around -1270 mV, -1450 mV and -1800 mV. The last one with the potential -1800 mV is probably the main peak given by reduction of carboxylic group of side chain of steroid skeleton. By cyclic voltammetry was determined that the process is quasireversible and is strongly influenced by adsorption of DHCA on the electrode surface and also by the pH which determines dissociation degree of carboxylic group. In the environment of BR buffer (pH 7.0) - methanol (9:1) was measured concentration dependence by DC, DP and "square-wave" voltammetry. By neither one of these methods have been reached satisfying limits of detection and wide linear dynamic ranges. However, the repeatable signals in wide range of pH can be used for electrochemical characterization of DHCA. CDCA offers in environment 0,04 mol·l-1 borat buffer (pH 9.1) - methanol (9:1) one signal with potential around -1350 mV. Position of this peak on the potential axe and also its height are...
Study of redox and adsorption features of bile acids on hanging mercury drop electrode
Yershova, Polina ; Schwarzová, Karolina (advisor) ; Gajdár, Július (referee)
Bile acids are the end products of cholesterol metabolism and are important biological surfactants. The curved shape of their chains allows the cyclization of molecules, and the formation of a supramolecular structure. The goal of this thesis was to study the electrochemical and adsorption behavior of selected bile acids: lithocholic, deoxycholic and cholic acids. The measurements were carried out in the medium Brittonův-Robinson buffer:methanol in the ratio 9:1 using cyclic voltammetry and AC voltammetry methods and measuring the dependence of the differential capacitance Cd on the applied potential E. A hanging mercury drop electrode was used as a working electrode. The measurements showed that bile acids are adsorbed on the surface of the electrode and organizing themselves in self assembled monolayers (SAM). In our case we have observed formation of 2D condensed layers as specific form of SAM. Transfer techniques were used to demonstrate bile acid adsorption. A study of the behavior of lithocholic acid as a function of different pH values showed that only at pH 10.0 to 12.0 2D 2D condensation occurs, i. e. that at pH values in the range of 2.0 to 9.0 it is another type of adsorption. On AC voltammograms, there are a maximum of two areas in which peaks occur: the first is around -0.2 V and the...
Analysis of Products of Nontemplate Enzymatic Synthesis of DNA Oligonucleotides using Voltammetric Methods
Hermanová, Monika ; Havranová-Vidláková, Pavlína ; Ondráčková, Anna ; Fojta, Miroslav
Nontemplate DNA synthesis is a feature specific for a special type of DNA polymerase, terminal deoxynucleotidyl transferase (TdT). This enzyme is able. to randomly add nucleotides to a sintde-stranded DNA primer, provided the 3'OH end of the primer is accessible, Here we show that voltammetric analysis based on hanging mercury drop electrode (EPODE) and pyrolytic graphite electrode (PGE) enables to study this nontemplate DNA synthesis.
Electrochemical reduction of dehydrocholic and chenodeoxycholic acid at stationary mercury and amalgam electrodes
Patáková, Adéla ; Schwarzová, Karolina (advisor) ; Vyskočil, Vlastimil (referee)
This thesis deals with the study of electrochemical behaviour of dehydrocholic and chenodeoxycholic acid at stationary mercury-based electrodes - hanging mercury dropping electrode and silver solid amalgam electrode modified by a mercury meniscus. This is the first study of electrochemical behaviour of dehydrocholic acid which offers tree peaks with potentials around -1270 mV, -1450 mV and -1800 mV. The last one with the potential -1800 mV is probably the main peak given by reduction of carboxylic group of side chain of steroid skeleton. By cyclic voltammetry was determined that the process is quasireversible and is strongly influenced by adsorption of DHCA on the electrode surface and also by the pH which determines dissociation degree of carboxylic group. In the environment of BR buffer (pH 7.0) - methanol (9:1) was measured concentration dependence by DC, DP and "square-wave" voltammetry. By neither one of these methods have been reached satisfying limits of detection and wide linear dynamic ranges. However, the repeatable signals in wide range of pH can be used for electrochemical characterization of DHCA. CDCA offers in environment 0,04 mol·l-1 borat buffer (pH 9.1) - methanol (9:1) one signal with potential around -1350 mV. Position of this peak on the potential axe and also its height are...
Study of electrochemical behaviour of tauroursodeoxycholic acid at mercury-based electrodes
Pišnová, Kateřina ; Schwarzová, Karolina (advisor) ; Navrátil, Tomáš (referee)
This thesis deals with electrochemical behaviour of tauroursodeoxycholic acid (TUDCA) at silver solid amalgam electrode modified by mercury meniscus (m-AgSAE), polished silver solid amalgam electrode (p-AgSAE) and hanging mercury dropping electrode (HMDE). This thesis is a part of a bigger scientific research that deals with synthesis and characterization of supramolecular systems based on natural steroid compounds and its conjugates. TUDCA offers one reduction peak at m-AgSAE in the environment of Britton - Robinson buffer in range of pH 6.0 - 13.0. The potential of this peak is around −1200 mV. Using cyclic voltammetry was determined that the process on the electrode surface is quasireversible, the reduction is controlled by diffusion and the anodic process is controlled by adsorption. Concentration dependence measured at HMDE by direct current voltammetry in 0.04 mol∙l-1 borat buffer (pH 9.1) is linear in two concentration intervals - 1∙10-3 - 2∙10-4 mol∙l-1 and 1∙10-4 - 8∙10-6 mol∙l-1 of TUDCA. There was no linear dependence between the increase of concentration of TUDCA and the height of the peak obtained on amalgam electrodes by methods DC, DP, cyclic and "square-wave" voltammetry. On HMDE was in several short concentration intervals measured by a CV method a linear dependence of cathodic and...

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