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Comparison of contactless conductivity detection and direct UV detection sensitivity for electrophoretic determination of N-acetylaminosaccharides
Malý, Michal ; Křížek, Tomáš (advisor) ; Kozlík, Petr (referee)
is work deals with development and optimization of a method for separation and detection of N- acetylglucosamine and its dimer and trimer using capillary zone electrophoresis with contactless conductiv- ity detection. Separation and detection of these substances is possible if sodium hydroxide is used as back- ground electrolyte. Usage of another electrolyte such as disodium phosphate leads to unacceptable baseline noise level. Optimal conditions of this method are a background electrolyte concentration of 40 mmol dm−3 and voltage of 15 kV. e method is very sensitive to background electrolyte pH, used background electrolyte also causes rapid degradation of the inner capillary wall which is why this method has proven difficult to cali- brate properly. e developed method was compared to an already existing method which uses UV detection. e existing method has lower limits of detection and quantification and is less sensitive to working condi- tions. Limits of detection and quantification of the developed method are 34 µmol dm−3 and 104 µmol dm−3 respectively. Limits of detection and quantification of the method based on UV detection are 7 µmol dm−3 and 21 µmol dm−3 respectively. Limits of quantification are that of the analyte whose detection was the least sensitive which was the dimer in both...
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Characterization of self-assembling molecules and their application in capillary electrophoresis
Hodek, Ondřej ; Křížek, Tomáš (advisor) ; Čabala, Radomír (referee)
This diploma thesis deals with application of newly synthesized α-cyclodextrins derivatives, 2I -O-cinnamyl-α-cyclodextrin and 3I -O-cinnamyl-α-cyclodextrin, in capillary electrophoresis. Their unique feature lies in formation of cyclodextrin aggregates in an aqueous solution by inclusion of phenyl moiety of one molecule into cavity of another one. The influence of addition of 2I -O-cinnamyl-α-CD and 3I -O-cinnamyl-α-CD to background electrolyte (BGE) and its impact on effective mobilities of eighteen selected analytes were tested. Nine analytes were measured in the form of cations (aniline, antipyrine, L-histidine, D,L-tyrosine, D,L- phenylalanine, N-(1-naphtyl)ethylenediamine, 4-nitroaniline, p-aminoaceto-phenon and tyramine) and nine in the form of anions (N-acetyl-D,L-phenylalanine, N-acetyl-D,L-tryptophan, N-benzoyl-D,L-phenylalanine, N-boc-D,L-tryptophan, N-FMOC-D,L-valine, N-FMOC-alanine, N-FMOC-D,L-leucine, D,L-3-phenyllactic acid and (R)-(-)-mandelic acid). Electrophoretic mobilities of cations were tested in BGE at pH 2.2 and anions at pH 8.0. The measurements were conducted at 25 and 50 řC. At the beginning the buffer containing 2.5 mM TRIS was adjusted with phosphoric acid to pH 2.2. However, it was found, that phosphate anions might enter cyclodextrin cavity and disable potential...
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Determination of selected components in human urine with electrophoresis in short capillary.
Makrlíková, Anna ; Opekar, František (advisor) ; Jelínek, Ivan (referee)
Capillary zone electrophoresis is frequently used in various analyses. In this diploma thesis a hydrodynamic sample introduction method controlled by pressure pulse has been proposed for short-capillary electrophoresis. The base electrolyte flushes sample from the loop of a six-way sampling valve and is carried to the injection end of the capillary. At the time when the sample zone reached the capillary, a short pressure impulse is generated in the electrolyte stream, which provides injection of the sample into the capillary. Then the electrolyte flow is stopped and the separation voltage is turned on. The amount of sample introduced to the capillary is controlled by the duration of the pressure pulse. This new sample introduction method was tested in the determination of ammonia, histidine, creatinine, uric acid and hippuric acid in human urine and for rapid screening of the contents of the inorganic ions in cerebrospinal fluid and blood plasma. The determination was performed in a capillary with an overall length of 10,5 cm and two base electrolytes was tested - 50 mM MES + 5 mM NaOH (pH 5,10) and 1 M acetic acid + 1,5 mM crown ether 18-crown-6 (pH 2,40). Using dual detection techniques contactless conductivity and UV spectrometric detection, anorganic and organic substances in the sample could...
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Determination of Lithium in Mineral Waters Using Electrophoresis in Short Capillary.
Makrlíková, Anna ; Opekar, František (advisor) ; Tůma, Petr (referee)
The aim of this study was determination of lithium ion concentration in mineral waters "Vincentka" and "Bílinská kyselka" using capillary electrophoresis with contactless conductivity detection. A specialized laboratory-made apparatus designed for separations in short capillaries was first tested for separation of model solution of common inorganic cations and then for analysis of mineral water samples. Lithium ion concentration was determined using method of standard addition. The results obtained were compared with those obtained from atomic absorption and emission spectroscopy; standard addition method as well as the method of calibration graph were used in spectroscopic methods. A good agreement was obtained between experimentally determined concentrations of lithium and those declared in the labels on the mineral water bottles. Keywords Capillary electrophoresis, contactless conductivity detection, mineral waters, lithium, atomic absorption spectroscopy, atomic emission spectroscopy
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Capillary electrophoresis with dual optical and contactless conductometric detection.
Kadlecová, Tereza ; Opekar, František (advisor) ; Jelínek, Ivan (referee)
This work deals with dual detection of organic and inorganic analytes after separation by capillary zone electrophoresis. In the first part, two types of hydrodynamic sampling are tested. Standard hydrodynamic sampling most often used in laboratory-made electrophoretic apparatus, based on lifting the vessel with the sample, in which the sampling end of the capillary is immersed, and a new method based on increasing the pressure in the sampling vessel without moving the capillary. This sampling procedure minimizes experimenter activity because it is controlled by software. Experimenter only changes vessel containing the sample solution for one with separation electrolyte. The experimental parameters, the sampling time and pressure, are optimized to achieve maximum separation efficiency and adequate detection sensitivity. In the second part of the work, the developed method is tested for the separation of amino-acids in a biological sample (urine).
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Determination of hyaluronan by electromigration methods
Bártová, Adéla ; Mravcová, Ludmila (referee) ; Řezáčová, Veronika (advisor)
This thesis is focused on description hyaluronic acid, characterization of its behaviour in water solutions, its chemical-physical properties and its using in different industrial sectors. The next part deals with possibilities of its analysis. The following section of the thesis is focused on electromigration techniques with special attention dedicated to capillary electrophoretic methods, especially capillary zone electrophoresis. The aim of this thesis is optimization of the method of determination of hyaluronic acid in water solutions by capillary zone electrophoresis.
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Comparison of gel and capillary electrophoresis of proteins
Krbec, Michal ; Franěk, Tomáš (advisor) ; Kotaška, Karel (referee)
Electrophoresis of serum proteins is one of the methods used in laboratory diagnosis of pathological conditions, but also for research purposes. This is a one-step method, which involves isolation of individual proteins from a mixture (mostly blood proteins) in the electric field in the presence of a suitable buffer and a suitable carrier based on their different mobility, dependent on their surface charge and molecular weight. Originally the carrieer used to be a paper, later cellulose acetate membrane and now it is almost exclusively agarose (purified agar with low endoosmosis) or polyacrylamide (PAA). My task in this work was to analyze a serie of samples by gel electrophoresis and subsequently analyze the same serie by capillary electrophoresis. Results obtained by both methods I worked numerically, compared with each other and statistically evaluated. The output of my work is a comparison of gel and capillary electrophoresis, evaluation of the advantages, disadvantages and especially the differences between these two methods.
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Analysis of pterine derivatives by capillary zone electrophoresis
Krajíček, Jan ; Bosáková, Zuzana (advisor) ; Čabala, Radomír (referee)
Pterins belong to an important group of compounds, acting as inhibitors, sensiziters, enzymes, coenzymes, pigments etc. and together with carotenoids and anthraquinones are responsible for characteristic coloration of bugs. This work was focused on the development of a capillary electrophoretic separation method for the analysis of six pterine derivatives, namely biopterine, neopterine, isoxanthopterine, leukopterine, xanthopterine and erythropterine and on their identification in the real samples. Separation was conducted in an uncoated fused-silica capillary termostated at 30 řC. Separation electrolyte contained boric acid, tris(hydroxymethyl)aminomethane and disodium salt of ethylenediaminetetraacetic acid. The effects of buffer pH, concentration of electrolyte components, separation voltage and wavelength of UV detection on electromigration behavior and detection sensitivity were studied. Under the optimized separation conditions, organic extracts of the three forms of Graphosoma semipunctatum bugs were analyzed.
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