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Utilization of tissue cultures for toxicology of the environment.
Polanská, Daniela ; Cajthaml, Tomáš (advisor) ; Klusoň, Petr (referee)
5 Abstract Five substances from the group of so-called personal care products, known for their low degradability and regular environmental detection, were tested for toxicity using two fish tissue lines (RTgill-W1 a RTG-2) isolated from rainbow trout (Oncorhynchus miykiss). The tested substances were hexadecylpyridinium chloride (HDP), chlorhexidine (CHX), octenidine (OCT), thymol (THM) and triclosan (TCS). A cell viability assay was performed with each of these compounds using Alamar Blue ™ (AB), 5-carboxyfluorescein diacetate acetoxymethyl ester (CFDA-AM) and neutral red (NR) protocols. The results were used to construct dose-response curves along with an EC50 value for each of these substances. The EC50 values ranged from 0,51 (HDP) to 33,75 µg.ml-1 (THM) for RTgill-W1 and from 0,31 (HDP) to 33,37 µg.ml-1 (THM) for RTG-2. The theoretical LC50 estimation was calculated according to Tanneberger et al. (2013). For all substances, cytochrome P450 1A activity was monitored using 7-ethoxyresorufin-o-deethylase (EROD), four out of five tested chemicals were statistically positive for EROD, the highest EROD response was observed for the most toxic compound - HDP. Only TCS did not show statistically significant cytochrome P450 1A activity. In addition, oxidative stress was measured with the fluorescent dye...
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Relaxivity of magnetic iron oxide nanoparticles containing diamagnetic cations
Kubíčková, Lenka ; Kohout, Jaroslav (advisor) ; Chlan, Vojtěch (referee)
Magnetic nanoparticles have received extensive attention in the biomedical research, e.g. as prospective contrast agents for T2-weighted magnetic resonance imaging. The ability of a contrast agent to enhance the relaxation rate of 1 H in its vicinity is quantified by relaxivity. The main aim of this thesis is to evaluate the transversal re- laxivity of ε-Fe2−x Alx O3 nanoparticles coated with amorphous silica or citrate - its dependence on external magnetic field, temperature and thickness of silica coating - by means of nuclear magnetic resonance. The aluminium content x = 0.23(1) was determined from XRF, the material was further characterised by XRPD, Möss- bauer spectroscopy, DLS, TEM and magnetic measurements. The size of magnetic cores was ∼ 21 nm, the thickness of silica coating ∼ 6,10,17 and 21 nm. Magne- tization of the ε-Fe2−x Alx O3 nanoparticles increased by ∼ 30 % when compared to ε-Fe2O3. The saturating dependence of relaxivity on external magnetic field and on the linear decrease with increase of thickness of silica coating contravene the theo- retical model of motional averaging regime (MAR); nevertheless, the temperature dependence acquired in 0.47 T and 11.75 T may be explained by MAR. In compari- son to ε-Fe2O3 nanoparticles, the relaxivity of examined samples was higher for par-...
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Cell viability changes after interaction with TiO2 nanoparticules and anthracycline cytostatics
Kondělková, Regina ; Štenglová Netíková, Irena (advisor) ; Merta, Ladislav (referee)
The goal of this thesis is to conduct a literary research about cell viability changes after interaction with TiO2 nanoparticules and anthracycline cytostatics. Anthracycline cytotoxic agents are one of the most commonly used groups of antineoplastic drugs, particulary doxorubicin. A serious side effect of anthracyclines in para drug administration (extravasation) is necrosis of the surrounding tissue. Effective treatment for this side effect is not available as of yet. One possible way could be to use sorption and degradation characteristics of nanoparticles of TiO2, which are non-toxic to the human body. Anthracyclines are characterized by rapid adsorption to the surface of nanoparticles of TiO2 and subsequent degradation to non-toxic products. Therefore further I deal with the use of nanoparticles of TiO2, their unique chemical properties and the way they affect cell viability, especially keratinocyte cell lines in vitro. It has been shown that there is no reduction in cell viability when culturing keratinocytes together with TiO2 nanoparticles and thus it opens the door for further studies on the use of nanoparticles of TiO2 for the treatment of necrotizing anthracycline extravasation.
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Cell Viability Measurement
Pelc, Pavel ; Janoušek, Oto (referee) ; Čmiel, Vratislav (advisor)
This work discusses the viability of cells. It describes the principle of fluorescence, fluorescent methods, fluorescent microskopy and the method of dyeing of the cells with a special kit that contains calcein AM and ethidium homodimer dyes. Further it describes the program for analysis and evaluation of viability on two different cellular cultures.
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Viability evaluation on cultivated mezenchymal cells
Jehličková, Jana ; Odstrčilík, Jan (referee) ; Čmiel, Vratislav (advisor)
This thesis deals with the possibilities of cell viability determination and its evalution. The thesis in theory describes cell cultivation, different methods of staining cells and display options. In the practical part is mentioned the preparation of the observed experiment and there are shown the examples of cell images created by confocal microscopy. Additionaly there are created the data analysis algorithm in Matlab. For setting suitable analysis parameters is formed user interface.
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Cell Viability Measurement
Prokopyeva, Elena ; Sekora, Jiří (referee) ; Čmiel, Vratislav (advisor)
This master's thesis deals with the ways of cell viability determination and its measuring. The first part of this thesis has a brief introduction into the theory of cell viability, also the methods of cell viability measurement and different types of fluorescent probes are described. The thesis further includes a brief description of the image processing methods, as well as the fluorescent microscope and applied filters are described. In the practical part the system implemented at a graphical programming environment LabVIEW used for the cell viability evaluation is described, functions of applied units are explained. The program is checked on model data.
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