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Preparation and characterization of hydrogels based on cationic biopolymer
Tesařová, Barbora ; Mravec, Filip (referee) ; Smilek, Jiří (advisor)
Presented thesis deals with the preparation and characterization of hydrogels based on positively-charged biopolymer and negatively-charged tenside. As an appropriate representative of positively-charged polymer was chosen chitosan, because of his biocompatibility and biodegrability, and N,N,N-trimethylchitosan, which was synthetised from chitosan in this diploma thesis. The final product of synthesis was characterised by SEC-MALS, elemental analysis, infrared spectroscopy and nuclear magnetic rezonation. Interactions between these polymers and representatives of negatively-charged tensides, which are sodium dodecylsuphate and sodium tetradecylsulphate, were investigated. The main method used in this thesis was rheology, through it were investigated prepared hydrogels based on chitosan and tensides and also prepared microgels based on N,N,N-trimethylchitosan and tensides. The interactions between polymers and tensides have been proved.
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Bio-inspired uracil building blocks as terminal functional groups for electronic materials
Krusberský, Vojtěch ; Ivanová, Lucia (referee) ; Richtár, Jan (advisor)
This bachelor thesis focuses on synthesis, purification and characterization of bio-inspired electron-accepting motifs based on N,N’-dialkylated barbituric acid derivatives for potential applications in the field of N-type organic semiconductors. The theoretical part deals with organic semiconductors and principles of their conductivity. Further covered topics are uracil, barbituric acid and its derivatives, synthetic approaches to target molecules and their analogues are also included. Within the experimental part two types of alkyl substituents were chosen – a flexible butyl and a bulky and rigid adamantylethyl. Both were incorporated into the structure via appropriate dialkylurea, which underwent condensation in the next phase. The final step of the synthetic route was the Knoevenagel condensation with a -conjugated trimer.
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Synthesis of soluble nature-inspired N, N-alkylated riboflavin derivatives, study of the effect of alkyl groups
Ivanová, Lucia ; Maier,, Lukáš (referee) ; Krajčovič, Jozef (advisor)
By flavin's unique structure, nature predestined riboflavin and its derivatives to the participation in redox processes within the bodies of all the living organisms. These biomolecules draw attention with intriguing optical properties and photosensitising abilities. Nature-inspired flavin derivatives share these qualities, and there is also a possibility of fine-tuning for the particular application from the chemical point of view. The thesis deals with two main aims. The first aim handles the synthesis of the trimer heteroaromatic precursor and 1,2-diketone. These key intermediates are essential for the future synthesis of the central aromatic core of the novel NH-free non-fused flavin derivative. The thesis introduces and verifies three approaches, including oxidation of diarylalkynes, nucleophilic addition of a corresponding organolithium compound to a Weinreb amide and benzoin condensation. The second aim covers the properties customization of NH-free fused systems by implementation of linear and bulky alkyl side-chains on the nitrogen atoms N1 and N3 of the alloxazine dilactam. N,N-alkylation introduced an increase in solubility in common organic solvents dichloromethane and chloroform. For the derivatives with 2-(adamantan-1-yl)ethyl substituents, high thermal stability was observed via TGA.
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Interaction of trimethylchitosan with Niaproof surfactant
Zbořilová, Hana ; Krouská, Jitka (referee) ; Mravec, Filip (advisor)
This thesis is focused on the study of interaction of the polycation N,N,N-trimethylchitosan (TMC) with the anionic surfactant Niaproof® 4 in water and physiological saline solution. Due to the commercial unavailability of N,N,N-trimethylchitosan, the polymer was first synthesized from chitosan, followed by NMR and FTIR characterization. Before the study of the system polycation–anionic surfactant itself, the behavior of the anionic surfactant Niaproof® 4 in aqueous solution and physiological saline solution was explored. The micellization of the surfactant Niaproof® 4 and the aggregation of TMC–Niaproof® 4 system were observed by fluorescence spectroscopy using the fluorescence probe pyrene. Values of critical micelle and critical aggregation concentration were determined on the basis of measurements. It was confirmed that presence of the sodium chloride supports the micellization by increasing the ionic strength of the solution, which leads to decrease of CMC in physiological saline solution. The interaction of TMC–Niaproof® 4 occurs at lower concentration then CMC in both aqueous and physiological environments. Phase separation occurs at higher concentrations of the surfactant leading to stabilization of the system.
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Study of membrane properties of liposomal systems using fluorescence spectroscopy
Zbořilová, Hana ; Pekař, Miloslav (referee) ; Mravec, Filip (advisor)
The presented diploma thesis is focused on the preparation, characterization and study of membrane properties of liposomal systems which were composed of the neutral phosphatidylcholine (DPPC), cholesterol, negatively charged phosphatidylglycerol (DPPG), polyethylenglycol bounded to phosphatidylethanolamine (PEG5000–PE) and polycation N,N,N-trimethylchitosan (TMC). The influence of individual components and their concentrations on the average particle size, zeta potential and changes in the outer and inner part of the bilayer was investigated. In this matter, methods of dynamic and electrophoretic light scattering and fluorescence spectroscopy with the application of laurdan and DPH probes were used. Based on the above-mentioned parameters, concentrations of components that most suitably influence properties of liposomes in terms of the intended application were selected for the definite complex. It was managed to prepare a liposomal complex stealth liposome–N,N,N-trimethylchitosan, which, due to the optimized composition, could have suitable attributes as a drug delivery system for inhalation administration of biologically active substances.
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Creation of instructional DVD rescue and first aid in the aquatic environment for students of high pedagogical schools
MIČAN, Richard
The bachelor thesis called ?Creation of instructional DVD of rescue and first aid in water environment for university students? deals with crisis situations, which can easily occur in water environment. These crises threaten the life-threatened often and, without first aid, endanger the consequences. People get close to the aquatic environment at work, during transport, recreation, or regeneration throughout the year. The main goal is to create an educational DVD about the rescue from the aquatic environment through literature and practical experience. The theoretical part of the thesis describes the basic skills, which are then transferred to the audiovisual form in the practical part. The benefit and efficiency of the instructional DVD has been tested on respondents. The instructional video is intended for university students. However, it can also be used by teachers, wider and professional public.
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Bio-inspired uracil building blocks as terminal functional groups for electronic materials
Krusberský, Vojtěch ; Ivanová, Lucia (referee) ; Richtár, Jan (advisor)
This bachelor thesis focuses on synthesis, purification and characterization of bio-inspired electron-accepting motifs based on N,N’-dialkylated barbituric acid derivatives for potential applications in the field of N-type organic semiconductors. The theoretical part deals with organic semiconductors and principles of their conductivity. Further covered topics are uracil, barbituric acid and its derivatives, synthetic approaches to target molecules and their analogues are also included. Within the experimental part two types of alkyl substituents were chosen – a flexible butyl and a bulky and rigid adamantylethyl. Both were incorporated into the structure via appropriate dialkylurea, which underwent condensation in the next phase. The final step of the synthetic route was the Knoevenagel condensation with a -conjugated trimer.
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Study of membrane properties of liposomal systems using fluorescence spectroscopy
Zbořilová, Hana ; Pekař, Miloslav (referee) ; Mravec, Filip (advisor)
The presented diploma thesis is focused on the preparation, characterization and study of membrane properties of liposomal systems which were composed of the neutral phosphatidylcholine (DPPC), cholesterol, negatively charged phosphatidylglycerol (DPPG), polyethylenglycol bounded to phosphatidylethanolamine (PEG5000–PE) and polycation N,N,N-trimethylchitosan (TMC). The influence of individual components and their concentrations on the average particle size, zeta potential and changes in the outer and inner part of the bilayer was investigated. In this matter, methods of dynamic and electrophoretic light scattering and fluorescence spectroscopy with the application of laurdan and DPH probes were used. Based on the above-mentioned parameters, concentrations of components that most suitably influence properties of liposomes in terms of the intended application were selected for the definite complex. It was managed to prepare a liposomal complex stealth liposome–N,N,N-trimethylchitosan, which, due to the optimized composition, could have suitable attributes as a drug delivery system for inhalation administration of biologically active substances.
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Synthesis of soluble nature-inspired N, N-alkylated riboflavin derivatives, study of the effect of alkyl groups
Ivanová, Lucia ; Maier,, Lukáš (referee) ; Krajčovič, Jozef (advisor)
By flavin's unique structure, nature predestined riboflavin and its derivatives to the participation in redox processes within the bodies of all the living organisms. These biomolecules draw attention with intriguing optical properties and photosensitising abilities. Nature-inspired flavin derivatives share these qualities, and there is also a possibility of fine-tuning for the particular application from the chemical point of view. The thesis deals with two main aims. The first aim handles the synthesis of the trimer heteroaromatic precursor and 1,2-diketone. These key intermediates are essential for the future synthesis of the central aromatic core of the novel NH-free non-fused flavin derivative. The thesis introduces and verifies three approaches, including oxidation of diarylalkynes, nucleophilic addition of a corresponding organolithium compound to a Weinreb amide and benzoin condensation. The second aim covers the properties customization of NH-free fused systems by implementation of linear and bulky alkyl side-chains on the nitrogen atoms N1 and N3 of the alloxazine dilactam. N,N-alkylation introduced an increase in solubility in common organic solvents dichloromethane and chloroform. For the derivatives with 2-(adamantan-1-yl)ethyl substituents, high thermal stability was observed via TGA.
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Interaction of trimethylchitosan with Niaproof surfactant
Zbořilová, Hana ; Krouská, Jitka (referee) ; Mravec, Filip (advisor)
This thesis is focused on the study of interaction of the polycation N,N,N-trimethylchitosan (TMC) with the anionic surfactant Niaproof® 4 in water and physiological saline solution. Due to the commercial unavailability of N,N,N-trimethylchitosan, the polymer was first synthesized from chitosan, followed by NMR and FTIR characterization. Before the study of the system polycation–anionic surfactant itself, the behavior of the anionic surfactant Niaproof® 4 in aqueous solution and physiological saline solution was explored. The micellization of the surfactant Niaproof® 4 and the aggregation of TMC–Niaproof® 4 system were observed by fluorescence spectroscopy using the fluorescence probe pyrene. Values of critical micelle and critical aggregation concentration were determined on the basis of measurements. It was confirmed that presence of the sodium chloride supports the micellization by increasing the ionic strength of the solution, which leads to decrease of CMC in physiological saline solution. The interaction of TMC–Niaproof® 4 occurs at lower concentration then CMC in both aqueous and physiological environments. Phase separation occurs at higher concentrations of the surfactant leading to stabilization of the system.
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