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Determination of double bond position in wax esters by dimethyl disulfide derivatization and mass spectrometry
Háková, Martina ; Schwarzová, Karolina (advisor) ; Coufal, Pavel (referee)
Wax esters are substantial constituents of natural waxes, which can be found in many living organisms. Properties of lipids, including wax esters, may be significantly influenced by the position of double bond. In this diploma thesis the location of double bonds was determined by dimethyl disulfide (DMDS) derivatization followed by detection using tandem mass spectrometry with atmospheric pressure chemical ionization (APCI) and electrospray ionization (ESI). We managed to measure the APCI and ESI MS/MS spectra of 8 different wax esters with different position of double bond. Diagnostic ions determining double bond position were identified. This method could be used in HPLC/MS analysis of wax esters, which cannot be analyzed by GC/MS. It was shown that the DMDS derivatization reaction and mass detection with APCI ionization is also suitable for locating double bonds in alkenes.
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The utitilization of boron-doped diamond thin film electrode for the voltammetric and amperometric determination of amino derivatives of biphenyl
Maixnerová, Lucie ; Schwarzová, Karolina (advisor) ; Zima, Jiří (referee)
The aim to this work was to develop methods for the determination of 2 aminobiphenyl (2-AB), 3 aminobiphenyl (3-AB), and 4-aminobiphenyl (4-AB) in model mixtures. Concretely, the direct determination of the mixture of studied analytes has been tested using spectrophotometry and differential pulse voltammetry (DPV). Furthermore, separation and detection of 2-AB, 3-AB, and 4-AB have been performed using high performance liquid chromatography with electrochemical detection (HPLC-ED) with boron-doped diamond film thin electrode (BDDFE) in ,,wall-jet" configuration and using high performance liquid chromatography with UV detection (HPLC-UVD). It was found out that the spectrophotometric determination of 2-AB, 3-AB, and 4-AB is impossible in their mixture because of nearby values of local absorption maxima wavelengths of all three analytes studied. Upon the determination of 2-AB, 3-AB, and 4-AB in their mixture using DPV in BR buffer pH 2.0, the difference in peak potentials of 2-AB and 3-AB is too low for their determination in mixture. Upon the determination of mixture containing 2-AB and 4-AB in BR buffer pH 12.0, the limits of determination (LDs) were obtained in the concentration order of 10-6 mol.l-1 for 2-AB and 10-7 mol.l-1 for 4-AB. LDs for the mixture containing 3-AB and 4-AB were obtained in the...
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Determination of selected terpenoids by HPLC with electrochemical detection
Mužíková, Jana ; Dejmková, Hana (advisor) ; Schwarzová, Karolina (referee)
This thesis deals with the determination of carvacrol, thymol, and eugenol by HPLC with electrochemical detection. Carbon paste electrode and boron doped diamond film electrode were used as the working electrodes. For the comparison, UV spectrophotometric detection at 275 nm was used besides the electrochemical detection. The separation was performed on LiChroCART 125-4, RP-18e (5 µm) column. Optimum separation conditions were found: mobile phase consisting of acetonitrile and acetate buffer in ratio 50:50, the optimum buffer pH was pH 5. The optimum potential of working electrode during electrochemical detection was +0,8 V and +1,2 V for carbon paste electrode and boron doped diamond film electrode, respectively. For both electrodes, repeatability of the measurement was examined; the surface of both electrodes had to be renewed between the measurements. Under the obtained optimum conditions, calibration dependences were measured. The studied substances were determined in real samples, in Thymus vulgaris L. and Achillea millefolium L. and in thyme-containing tea and syrup.
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Voltammetric detection of stigmasterol at boron-doped diamond electrode in mixed media
Benešová, Lenka ; Schwarzová, Karolina (advisor) ; Nesměrák, Karel (referee)
V o l t a m m e t r i c d e t e c t i o n o f s t i g m a s t e r o l a t b o r o n d o p e d d i a m o n d e l e c t r o d e i n m i x e d m e d i a L e n k a B e n e š o v á Univerzita Karlova v Praze Přírodovědecká fakulta Praha 2015 Abstract The aims of the study thesis was to suggest suitable solvent for oxidation of stigmasterol on boron doped diamond electrode. Cyclic voltammetry in mixed media of water and organic solvents was used for this purpose. First of all, the effect of organic solvent on potential window of boron doped diamond electrode was studied. Solvents used were methanole, isopropanole, N-dimethylformamide and acetonitrile; the water components was phosphate buffer (0,075 mol.l-1, pH 3,0). It was deduced from the results, that suitable solvent for detection of stigmasterol on was the acetonitrile, which provided sufficiently large potential window in anodic area. Keywords: boron doped diamond electrode, cyclic voltammetry, organic solvent, oxidation, stigmasterol
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Electrochemical determination of 6-thioguanine at boron doped diamond film electrod
Humpolíková, Jiřina ; Fischer, Jan (advisor) ; Schwarzová, Karolina (referee)
This master's thesis is focused on the determination of 6-thioguanine (6-T) by DC voltammetry (DCV), differential pulse voltammetry (DPV) and flow injection analysis with electrochemical detection (FIA-ED) on a boron doped diamond electrode (BDDFE). The optimum conditions for determination of 6-T were found and under these conditions, concentration dependences were measured and the limits of quantification (LOQ) were calculated for each method. Medium of 60% methanol and phosphate buffer (PB) pH 2,0 was chosen as optimum for DCV and DPV determination of 6-T at BDDFE. For both DCV and DPV, the linear concentration dependences were obtained in concentration ranges of 6-T from 2 µmol·l-1 to 10 µmol·l-1 with LOQ 0,9 µmol·l-1 for DCV and 1,5 µmol·l-1 for DPV. Lower LOQ was achieved in PB pH 2,0, where LOQ was 0,6 µmol·l-1 for both DCV and DPV, but the problem was lower repeatability. In PB pH 2 6-T was determined by DCV in drinking and river water with LOQ 1,3 µmol·l-1 in both drinking and river water. The possibility of solid phase extraction was investigated as a method for preliminary separation of 6-T from urine. For FIA under optimized conditions (polarization potential 1300 mV, flow rate 5 ml·min1 and sample volume 50 µl) the linear concentrations dependences were obtained in concentration ranges...
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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...
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Determination of carvacrol using HPLC with electrochemical detection
Mužíková, Jana ; Dejmková, Hana (advisor) ; Schwarzová, Karolina (referee)
This thesis deals with determination of a mixture of carvacrol with thymol and eugenol by HPLC with electrochemical detection. Carbon paste electrode was used as the working electrode. The separation was performed on Kromasil-C18, 250x4,6 mm column. For the comparison, UV spectrophotometric detection at 275 nm was used besides electrochemical detection. Optimal separation conditions were found: mobile phase consisting of acetonitrile and phosphate buffer in ratio 60:40, the optimal buffer pH was pH 4. As the optimum potential of working electrode during electrochemical detection, potential +1.1 V was found. Under the obtained optimal conditions, calibration dependences were measured. Limit of quantification for carvacrol was found to be 9,6·10-7 mol dm-3 using UV spectrophotometric detection and 4,0·10-8 mol dm-3 using electrochemical detection.
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Development and application of electrochemical flow-through detector with renewable working material
Mika, Jan ; Dejmková, Hana (advisor) ; Schwarzová, Karolina (referee) ; Metelka, Radovan (referee)
The aim of this thesis was development and initial testing of new porous electrochemical detector for flow-through arrangements, especially for flow injection analysis (FIA) and liquid chromatography. One of the most advantageous properties of the detector is simple renewal of working material and thus its suitability for determination of strongly passivating substances. Glassy carbon microbeads and copper microparticles were tested as a working material within this study. Initially, basic electrochemical properties of the glassy carbon-based detector were examined by FIA using hydroquinone and potassium ferrocyanide as model substances. For both model substances high degree of conversion was achieved (around 100 %), and thus it was concluded that glassy carbon-based detector can be considered as coulometric. Hereafter, practical application of the carbon-based detector are presented on five electrochemically active substances closely related to the human medicine and pharmacy - thymol, tyrosine, sulfamethizole and vanillylmandelic acid (VMA) simultaneously determinined with homovanillic acid (HVA). Complexity of instrumental arrangement of flow-through methods had been increasing consecutively up to the HPLC determination with gradient programme. It was proved that the carbon-based detector is...
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Porous Boron-Doped Diamond Electrodes: Characterisation and Application for Electroanalysis
Baluchová, Simona ; Schwarzová, Karolina (advisor) ; Navrátil, Tomáš (referee) ; Šelešovská, Renáta (referee)
This dissertation thesis presents newly developed electrode materials based on porous boron- doped diamond (BDDporous) and their potential applications in electroanalysis. Particularly, these novel BDDporous electrodes (twelve in total) were thoroughly electrochemically characterised and compared, and the ones with the most promising properties were selected to develop reliable voltammetric methods for detecting the neurotransmitter dopamine. Initially, the impact of selected fabrication parameters on the final properties and electrochemical behaviour of novel BDDporous electrodes was clarified; the following factors were specifically studied: (1) deposition template used, (2) boron-doping level, (3) growth time of the individual layers (i.e., porosity), (4) number of deposited layers (i.e., thickness), and (5) content of non-diamond (sp2 ) carbon impurities. Alterations in deposition conditions naturally resulted in BDDporous electrodes with diverse (i) structural and morphological features, which were investigated by scanning electron microscopy and Raman spectroscopy, and (ii) physical and electrochemical characteristics, examined by cyclic voltammetry. Besides, to assess the suitability of selected BDDporous electrodes for dopamine detection, other parameters, such as susceptibility to...
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