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Ruthenium-based nanoparticles and testing of their anticancer activity
Žáková, Eliška ; Fohlerová, Zdenka (referee) ; Heger,, Zbyněk (advisor)
Neoplastic diseases hold the second place of the most common causes of death worldwide. Available treatments include various combinations of surgery, chemotherapy, radiation, hormone therapy, immune therapy and targeted therapy. The emphasis is currently laid on nanomedicine, where new nanosized complexes are developed and applied for the targeted treatment and chemotherapy. The aim is to significantly improve the anticancer effect and decrease the damage to organism. In this thesis, ruthenium nanoparticles with a size of 12–14 nm were synthesized and their surface modified with polyvinylpyrrolidone. Furthermore these were subsequently modified with polyoxyethylene(40)stearate for binding of doxorubicin. These nanoparticles were tested on breast carcinoma cells (MDA-MB-231), ovarian carcinoma cells (A2780) and neuroblastoma cells (UKF-NB-4). Apoptosis and necrosis testing showed 60—64 % increase in apoptosis when comparing ruthenium nanoparticles modified with doxorubicin to nonmodified ruthenium nanoparticles. The modification increased level of oxidative stress in tumorous cells and slightly a genotoxicity to non-tumorous cells, nevertheless the hemocompatibility was significantly improved. Testing has proven with IC50 0.98 g/ml, 3.91 g/ml and 1.95 g/ml higher sensitivity to these cells and confirmed expected anticancer activity. Compared to one of the most common chemotherapeutic agents cisplatin the modified ruthenium nanoparticles are significantly more toxic to cell lines A2780 (IC50=21 µg/ml), MDA-MB-231 (IC50=9 µg/ml) and UKF-NB-4 (IC50=4 µg/ml).
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The study of metallocene anticancer therapeutics-cells interaction
Bilavčíková, Kristýna ; Mravcová, Ludmila (referee) ; Vašinová Galiová, Michaela (advisor)
There were almost 600 thousand patients in Czech Republic until 2017 and the number keeps rising. Chemotherapeutics used today have lots of undesirable side effects, so scientists around the world are trying hard to find more specific and less cytotoxic drugs. In this bachelor’s thesis, potential drugs based on metallocene with a central atom of Ru, Hf or Zr were studied, always in three different drugs for each element. The permeability and distribution of these drugs into lung cancer cell lines were investigated. These drugs were detected by analysis of solutions and laser ablation with an ICP mass spectrometer. Based on the experiment, the greatest potential was found for the ruthenium-based drug 133, which had the highest permeability and was able to get into the cells in the highest volume.
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UV-photochemical generation of volatile species of tellurium and other transition metals
Jeníková, Eva
This dissertation thesis is focused on UV-photochemical generation of volatile species of tellurium, ruthenium, rhenium and iridium coupled to methods of atomic spectrometry. In the first part, attention was paid to the optimization of parameters of UV-photochemical generation of volatile tellurium species and its application for speciation analysis of Te(IV) and Te(VI) in water samples. UV-photochemical generation was carried out in a UV-photoreactor, which consisted of a low-pressure mercury lamp wrapped with a polytetrafluoroethylene reaction coil that served as a reactor. Atomic absorption spectrometry with a continuum source of radiation and high resolution and atomization in a miniature diffusion flame were used to optimize the conditions of generation, which included the composition of the reaction medium, irradiation time and the addition of transition metals as modifiers. In order to achieve a higher sensitivity of determination, the generator was coupled to a triple quadrupole inductively coupled plasma mass spectrometer. Since efficient UV-photochemical generation of volatile species was achieved only from Te(IV), with no response from Te(VI), the feasibility of this technique for simple "non-chromatographic" speciation analysis was tested and a method for determination of Te(IV) and...
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UV-photochemical generation of volatile species of tellurium and other transition metals
Jeníková, Eva ; Hraníček, Jakub (advisor) ; Šíma, Jan (referee) ; Kanický, Viktor (referee)
This dissertation thesis is focused on UV-photochemical generation of volatile species of tellurium, ruthenium, rhenium and iridium coupled to methods of atomic spectrometry. In the first part, attention was paid to the optimization of parameters of UV-photochemical generation of volatile tellurium species and its application for speciation analysis of Te(IV) and Te(VI) in water samples. UV-photochemical generation was carried out in a UV-photoreactor, which consisted of a low-pressure mercury lamp wrapped with a polytetrafluoroethylene reaction coil that served as a reactor. Atomic absorption spectrometry with a continuum source of radiation and high resolution and atomization in a miniature diffusion flame were used to optimize the conditions of generation, which included the composition of the reaction medium, irradiation time and the addition of transition metals as modifiers. In order to achieve a higher sensitivity of determination, the generator was coupled to a triple quadrupole inductively coupled plasma mass spectrometer. Since efficient UV-photochemical generation of volatile species was achieved only from Te(IV), with no response from Te(VI), the feasibility of this technique for simple "non-chromatographic" speciation analysis was tested and a method for determination of Te(IV) and...
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The study of metallocene anticancer therapeutics-cells interaction
Bilavčíková, Kristýna ; Mravcová, Ludmila (referee) ; Vašinová Galiová, Michaela (advisor)
There were almost 600 thousand patients in Czech Republic until 2017 and the number keeps rising. Chemotherapeutics used today have lots of undesirable side effects, so scientists around the world are trying hard to find more specific and less cytotoxic drugs. In this bachelor’s thesis, potential drugs based on metallocene with a central atom of Ru, Hf or Zr were studied, always in three different drugs for each element. The permeability and distribution of these drugs into lung cancer cell lines were investigated. These drugs were detected by analysis of solutions and laser ablation with an ICP mass spectrometer. Based on the experiment, the greatest potential was found for the ruthenium-based drug 133, which had the highest permeability and was able to get into the cells in the highest volume.
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Reactivity of a ferrocene distibane
Antala, Jakub ; Štěpnička, Petr (advisor) ; Gyepes, Róbert (referee)
5 Title: Reactivity of ferrocene distibane Author: Jakub Antala Department: Department of Inorganic Chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Consultant: RNDr. Jiří Schulz, Ph.D. Abstract: The aim of this bachelor thesis is preparation of 1,1'-bis(diphenylstibino)ferrocene (L), an antimony analogue of the widely studied ligand 1,1'-bis(diphenylphosphino)ferrocene and study into its coordination properties. Two ruthenium(II) (1, 3) and two rhodium(III) complexes (2, 4) were prepaired, in which the ligand L coordinates as bridging or chelating ligand. Two ruthenium(II) and one rhodium(III) precursors with π-coordinated arene ligands were used for the preparation of complexes. When preparing chelate complexes, sodium hexafluorophosphate was also necessary. All complexes were characterised by NMR spectroscopy, mass spectrometry, elemental analysis and crystal structure was determined by X-ray structural analysis. The structures of the stibine complexes were compared with their analogs resulting from 1,1'-bis(diphenylphosphino)ferrocene. Key words: ferrocene, stibines, complexes, ruthenium, rhodium, structure elucidation
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Preparation and properties of building blocks of specialty polymers
Šichová, Kristýna
This Diploma Thesis presents results obtained by solution of two partial projects: a) Preparation of monomers from renewable sources using metathesis and tandem hydrogenation catalyzed with ruthenium compounds - project solved during my Erasmus stay at the Université de Rennes 1 in France; b) Preparation and properties of ,-bis(tpy)quarterthiophene oligomers carrying ionic side groups as oligomonomers for polyelectrolyte conjugated dynamers - project solved at the Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University in Prague. Project a): Self-metathesis of 1,2-epoxyhex-5-ene (but-3-enyloxirane) and its cross-metathesis with methyl acrylate and acrylonitrile catalyzed with ruthenium compounds as well as tandem design of these metatheses and consecutive hydrogenation of their products by gaseous hydrogen have been optimized. The following influences have been studied and tuned: (i) type of the catalyst (Grubbs, Hoveyda, Zhan) and its concentration and method of dosing, (ii) concentration of reactants and additives, (iii) type of solvent, and (iv) reaction temperature. Reactions were monitored by the GC, GC and MS methods and the products were characterized by the NMR method. Methyl 6,7-epoxyheptanoate (methyl 5-oxiranylpentanoate) obtained by the tandem...
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Light platinum group metal complexes with a ferrocene N-phosphinoamide
Navrátil, Michal
Title: Light platinum group metal complexes with a ferrocene N-phosphinoamide Author: Bc. Michal Navrátil Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Abstract: The aim of this diploma thesis is the preparation of coordination compounds containing ferrocene phosphinoamide FcCONHPPh2 (1, Fc = ferrocenyl), whose preparation was discussed in author's bachelor thesis. Twelve new complexes are described in this thesis, including their characterisation by NMR and infrared spectroscopy, elemental analysis and mass spectrometry. In all cases the crystal structure was determined. Two palladium(II), one rhodium(III) and one ruthenium(II) precursors were used for the preparation of the complexes with each providing three new compounds. A reaction of the precursors with phosphinoamide 1 yielded complexes, in which the phosphinoamide was P-coordinated. This compound was a precursor for the other two complexes. The first one was obtained by a reaction with silver(I) perchlorate producing a cationic P,O-chelate. The other was obtained by a reaction with potassium tert-butoxide resulting in neutral P,O- chelate. All twelve complexes were prepared with optimised yields. Keywords: ferrocene, amides, phosphines, palladium, rhodium, ruthenium, structure elucidation.
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Light platinum group metal complexes with a ferrocene N-phosphinoamide
Navrátil, Michal
Title: Light platinum group metal complexes with a ferrocene N-phosphinoamide Author: Bc. Michal Navrátil Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Abstract: The aim of this diploma thesis is the preparation of coordination compounds containing ferrocene phosphinoamide FcCONHPPh2 (1, Fc = ferrocenyl), whose preparation was discussed in author's bachelor thesis. Twelve new complexes are described in this thesis, including their characterisation by NMR and infrared spectroscopy, elemental analysis and mass spectrometry. In all cases the crystal structure was determined. Two palladium(II), one rhodium(III) and one ruthenium(II) precursors were used for the preparation of the complexes with each providing three new compounds. A reaction of the precursors with phosphinoamide 1 yielded complexes, in which the phosphinoamide was P-coordinated. This compound was a precursor for the other two complexes. The first one was obtained by a reaction with silver(I) perchlorate producing a cationic P,O-chelate. The other was obtained by a reaction with potassium tert-butoxide resulting in neutral P,O- chelate. All twelve complexes were prepared with optimised yields. Keywords: ferrocene, amides, phosphines, palladium, rhodium, ruthenium, structure elucidation.
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Light platinum group metal complexes with a ferrocene N-phosphinoamide
Navrátil, Michal ; Štěpnička, Petr (advisor) ; Gyepes, Róbert (referee)
Title: Light platinum group metal complexes with a ferrocene N-phosphinoamide Author: Bc. Michal Navrátil Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Abstract: The aim of this diploma thesis is the preparation of coordination compounds containing ferrocene phosphinoamide FcCONHPPh2 (1, Fc = ferrocenyl), whose preparation was discussed in author's bachelor thesis. Twelve new complexes are described in this thesis, including their characterisation by NMR and infrared spectroscopy, elemental analysis and mass spectrometry. In all cases the crystal structure was determined. Two palladium(II), one rhodium(III) and one ruthenium(II) precursors were used for the preparation of the complexes with each providing three new compounds. A reaction of the precursors with phosphinoamide 1 yielded complexes, in which the phosphinoamide was P-coordinated. This compound was a precursor for the other two complexes. The first one was obtained by a reaction with silver(I) perchlorate producing a cationic P,O-chelate. The other was obtained by a reaction with potassium tert-butoxide resulting in neutral P,O- chelate. All twelve complexes were prepared with optimised yields. Keywords: ferrocene, amides, phosphines, palladium, rhodium, ruthenium, structure elucidation.
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