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Portable liquid chromatograph and analyses of hazardous substances
Šesták, Jozef ; Gogaľová, Zuzana ; Kahle, Vladislav ; Lunerová, K.
Progress in technology of microchips, batteries and LEDs in the last two decades enable development of portable instruments which can satisfy the requirements of modern liquid chromatography (LC). Application of portable LC is advantageous if simple and rapid sample treatment procedure followed by a short HPLC run can be executed in the point of sampling. Our research group have developed a concept of portable HPLC based on simple hydraulic scheme and a unique optical detector for simultaneous detection of absorbance and fluorescence of compounds eluted off microcolumn. Considering in-field analysis of hazardous substances, this instrument can be advantageous for analysis of compounds which are difficult to detect and quantify by other contemporary portable instruments utilizing different working principles due to incompatibility with their physico-chemical properties (e. g. microbial toxins).
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Quantum dot luminescent probe for Caspase 3/7 imaging inside cells
Procházková, Markéta ; Klepárník, Karel
Two step synthesis of luminescent probe based on ligand-exchange in the first step and the specific reaction of amino group in the second step was optimized. The luminescence properties of the final product were checked by time course of\nactive recombinant caspase protein reaction under the model conditions in fluorimeter. The novel luminescent probe enables long-time imaging of active caspases in living cells or tissues.
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Epitachophoretic preconcentration of proteins
Hrušková, Helena ; Voráčová, Ivona ; Foret, František
In this work, we present a developed method for preconcentration of standards of proteins cytochrome c, myoglobin, and hemoglobin. Firstly, the electrolyte system was selected and optimized to provide low analysis time, narrow shape of the protein zone, and eliminate overheating at the center of the device. In the next step, the developed method was tested on the preconcentration of proteins: cytochrome c, myoglobin, and hemoglobin. After several adjustments myoglobin and hemoglobin were also uccessfully preconcentrated. After evaluation of pilot results, this technique provides up to fiftyfold preconcentration and recovery of over 70 % for each protein. The next plan is to preconcentrate proteins from complex biological matrices such as urine or blood plasma.
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