The aim of master thesis was to study structural and transport properties of PVA films modified with method of semi-IPN with suitable polyectrolytes and plasticizers. The first important step was optimalization of PVA films preparation, when time of heating was set at 90 °C for 1 hour. Drying was set at 50 °C for 24 hours. Molecular weight of PVA was chosen 85–124 kDa in concentration 10 wt.%. For preparation of PVA-based semi-IPN thin films polyelectrolytes (polyglutamic acid, DEAE-dextran hydrochloride) and plasticizer (glycerol) were selected. Basic characterization of prepared materials was performed with FTIR, TGA, SEM and specific surface analysis. The difference between modified PVA films was in the chargé of individual functional groups carried by used polyelectrolytes. Surfaces of all the PVA films were smooth without visible defects. Transport properties were characterized with the method of horizontal diffusion cell with methylen blue used as a probe. Diffusion coefficients of methylen blue through PVA films were determined. It was found, that the fastest pass was throw PVA film without additives. The slowest diffusion was observed through PVA/DEAE-dextran film, because of the same charge of the film with a probe. PVA/PGA reacted with methylen blue to form a complex. Plasticizer effect on the diffusion was only minor; it caused a slight decrease of diffusion coefficient. These films were easier to handle.

This diploma thesis deals with hyaluronan modified by palmitoyl and its gelation. Gels were created from palmitoyl hyaluronan with molecular weight 216 kDa and degree of substitution 11 % in concentrations 15 and 20 g dm-3 in water and concentrations 10, 15, 20 g dm-3 in NaCl and TSB. Also gel from palmitoyl hyaluronan with molecular weight 35 kDa and degree of substitution 10 % in concentrations 20, 30 g dm-3 in NaCl was created. Gels were investigated concerning medical applications. Gels were rigid and had very good properties, which was confirmed by rheology. The physical properties (pH, water content) of gels and stability were investigated. On the grounds of the MTT test, three methods of cell incorporation were suggested. Gels are nontoxic, biocompatible, and biodegradable with nontoxic degradation products and that is why they are excellent aspirants for use in biomedicine.

This diploma thesis investigates the suitability of relaxation tests as a part of complex characterization of hydrogel materials using classical rheology methods. With respect to the current research, creep and three interval thixotropy tests were taken into account. For them, general optimization was done aiming to find an ideal parameter settings. The optimization was performed using physically crosslinked agarose (AG) hydrogel and the tuned tests were also applied to two more samples: hyaluronan (HyA) and polyvinyl alcohol (PVAl) gel. These materials were selected due to their mutually different crosslinking principle. The experiments showed, the AG gel proved to have the best ability to recover after deformation of all studied samples. On the other hand, the HyA gel relaxed the worst. Although the final results of both tests were comparable, the regeneration process itself was different. Hence, the complex relaxation characteristics cannot be described using one of the performed tests alone and both the creep and three interval thixotropy tests have great importance in the scope of complex relaxation behaviour. The obtained results may lead to more precise description of deformation and relaxation, which are frequent phenomena occurring during treatment and application of hydrogel materials.

Tuberous sclerosis complex (TSC) is a multisystem tumor-forming disorder caused by biallelic inactivation of TSC1 or TSC2. The primary cause of mortality arises from mesenchymal manifestations in the lung and kidney: pulmonary lymphangioleiomyomatosis (LAM) and renal angiomyolipomas (RAMLs). Despite a well-described monogenic etiology, there remains an incomplete understanding of disease pathogenesis. Consequentially, tractable models which fully recapitulate disease characteristics are lacking. Here, I develop and study novel tissue-engineered models of TSC lung and kidney disease. In my first chapter, I demonstrate that lung-mimetic hydrogel culture of pluripotent stem cell-derived diseased cells more faithfully recapitulates human LAM biology compared to conventional culture on two-dimensional plastic. Leveraging this culture system, I conducted a three-dimensional drug screen using a custom 800-compound library, tracking cytotoxicity and invasion modulation phenotypes at the single cell level. I identified histone deacetylase (HDAC) inhibitors as a group of anti-invasive agents that are also selectively cytotoxic towards TSC2-/- cells. HDAC inhibitor therapeutic effects remained consistent in vivo upon xenotransplantation of LAM cellular models into zebrafish. In my second chapter, I develop a genetically-engineered human renal organoid model which recapitulates pleiotropic features of RAMLs in vitro and upon orthotopic xenotransplantation. I find that loss of TSC1/2 affects multiple developmental processes in the renal epithelial, stromal, and glial compartments. First, loss of TSC1/2 leads to an expanded stroma by favouring stromal cell fate acquisition and alters terminal stromal cell identity. Second, epithelial cells in the TSC1/2-/- organoids exhibit a rapamycin-insensitive epithelial-to-mesenchymal transition. Third, a melanocytic population forms exclusively in TSC1/2-/- organoids, branching from MITF+ Schwann cell precursors of a bona fide neural crest-to-Schwann cell differentiation trajectory. Through these two thesis chapters, I realize the power of tissue-engineered models for the study of TSC. This work offers novel insights into the pathogenesis of RAMLs and identifies a new class of therapeutics suitable for trialing in patients with pulmonary LAM.

For passive (classical) materials, stress and strain are used to extract the material behavior from the sample behavior in a tensile test. In analogy, the actuation behavior of active (smart) materials can be normalized. In the present research, we show the normalization using the example of hydrogels that react with a volume change (swelling and deswelling) when exposed to stimulus-changes like temperature, chemical concentrations, pH or light intensity changes. The normalized behavior can then be implemented with the Temperature-Expansion-Model which is based on the analogy of active behavior with thermal expansion. This allows the simulation of arbitrary active structures and the extraction of the sensitivity measure to a stimulus.

This thesis studies the properties and behaviour of phase-separated hydrogels prepared by interaction of hyaluronan with oppositely charged surfactants. Three representatives of surfactants, namely cetyltrimethylammonium bromide, chloride and p-toluensulfonate (CTAB, CTAC, CTAT), were selected for comparison. Using the method of rheology, the fact that the system of Hya-CTAT forms the most rigid hydrogels has been proved. Higher molecular weight of hyaluronan has also direct influence on the volume and stiffness of the newly formed hydrogels. Preparation methods were compared as well. Mixing the stock solutions of entry components appeard to be the most suitable. Small-angle X-ray scattering was used for determination of shape and size of surfactant's micelles, concluding that it has no effect on the volume of formed gels. The results of this study indicate that given gels are to a certain extent competitive and incorporation of hyaluronan into their structure is desirable with respect to its biological activity. This offers a potential usage of these substances in the field of medical applications.

This diploma thesis is focused on the determintaion of viscoelastic properties of agarose hydrogels containing different polyelectrolytes by microrheological and macrorheological techniques. From microrheological techniques the dynamic light scattering was used. Firstly, the influence of different polyelectrolyte volume was studied. Then the effect of variously charged polyelectrolyte and ionic strenght on microrheological properties of agarose hydrogels were determined. Classic rheology was used to compare the results obtained using the DLS microrheology method. Finally, the results from macro- and microrheology were correlated with each other.

This master's thesis is focused on study of transport processes in hydrogels based on humic acids. For this purpose is used methods unsteady diffusion in cuvettes, which was studied the transport of organic dyes, specifically methylene blue and rhodamine 6G, in agarose hydrogel without the addition and with the addition of individual standards humic acids (Leonardite, Elliott Soil, Suwannee River II and Pahokee Peat). This method is based on spectrophotometric monitoring of concentration changes of dyes depending on space of the cuvette and on time. The aim of this thesis was to investigate the effects of interactions between diffusing dye and the particular type of gel to the resultant effective diffusion coefficient of dye. The experiments indicate that the presence of humic acid in the hydrogel greatly affects the transport of selected dyes.

This diploma thesis was focused on study of barrier and transport properties of selected polyelectrolytes in hydrogel matrices by using diffusion techniques. The study of these properties was performed in horizontal diffusion cells where is observed the change in diffusion probe concentration over time. Diffusion experiments were performed on an agarose hydrogel with the addition of alginate, hyaluronic acid, polystyrene sulfonate, humic acids and as a model probe rhodamine 6G was used. Important parts of this thesis are also the methods which characterize the substances and hydrogel matrices such as rheology and potentiometric titration. The main aim of this diploma thesis was to investigate the effect of interactions between passing model dye (rhodamine 6G) and the appropriate gel (agarose + polyelectrolyte) on the fundamental diffusion parameters (effective diffusion coefficient, lag time, etc.).

The main goal of this work is design and synthesis of novel composite hydrogel-based core-shell microparticles and their application for fabrication of coatings, which provide the “inverse-switching” behaviour to the surface, namely, to become more hydrophobic in water environment. Since contact angle of heterogeneous surfaces is dependent on the nature and ratio of surface components, an increase of amount of more hydrophobic component on the surface will cause the reducing of surface wettability. It was suggested that core-shell particles having water-swellable hydrogel core and hydrophobic, but permeable for water shell when deposited on the hydrophilic substrate should increase the total amount of hydrophobic component on the surface when the cores of particles will swell in water. During the work different approaches to obtain freely dispersed and surface-immobilized core-shell particles with required structure were developed. Obtained particles were applied for preparation of coatings with ability to display “inverse-switching” behaviour. It was demonstrated that properly designed and properly prepared core-shell particles could be successfully used for creation of smart adaptive coatings having the ability to alter the surface properties upon changing of the environment.