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Control the molecular weight of hyaluronic acid (HA) by adjusting the specific growth rate of culture Streptococcus equi subsp. zooepidemicus
Osičková, Jana ; Pepeliaev,, Stanislav (referee) ; Franke,, Lukáš (advisor)
This master thesis focuses on the effect of cultivation parameters on hyaluronic acid synthesis during its biotechnological production. The cultivation parameters were temperature of the cultivation, aeration, agitation, carbon source and addition of phosphatidylcholine. Changes in molecular weight and yield of hyaluronic acid, growth of biomass and medium viscosity were observed. From the obtained data we learned, that the specific growth rate greatly impacts final characteristics of hyaluronic acid. Under suboptimal temperatures a high molecular weight polymer was synthesised along with comparable yields from the control cultivation. High temperatures (40 °C) caused a dip in molecular weight. The next cultivation parameters were aeration and agitation. The highest molecular weights were obtained in cultivations with high agitation rates and intensive aeration, specifically 1 vvm/800 rpm and 2 vvm/800 rpm. Agitation had a bigger influence on molecular weight than aeration. When the carbon source was changed from sucrose to glucose, the lowest molecular weight and yield were obtained. Addition of phosphatidylcholine with concentration 160 mg/l had a positive effect on the cultivation, where the molecular weight grew and biomass growth was higher.
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Direct Synthesis of High-Molecular Polymers of Lactic Acid
Mikulík, David ; Kupka, Vojtěch (referee) ; Petrůj, Jaroslav (advisor)
This master thesis deals with the direct synthesis of polymers from lactic acid. The theoretical part focuses on both natural and synthetic ways of production the lactic acid monomer, their advantages and properties. Furthermore, the theoretical part focuses on the synthesis of poly(lactic acid) (PLA) from lactide, and direct polycondensation from lactic acid discussing about influences of catalysts, co-catalysts as well as chain extenders. The experimental part focuses on the synthesis of PLA polymers and co-polymers wherein investigates suitable catalysts, reaction medium for azeotropic dehydration and co-catalyst influence on products. Thermal and analytical analysis of PLA polymers are mentioned at the end of the experimental part.
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Study of hyaluronan-albumin systems using light scattering methods and calorimetry
Sereda, Alena ; Hermannová, Martina (referee) ; Chytil, Martin (advisor)
This thesis, which is a continuation of the previous Bachelor thesis, is dedicated to the study of polyelectrolyte complexes between hyaluronan (HA) and bovine serum albumin (BSA). Interactions between HA and BSA and a formation of complexes were studied by SEC-MALLS method, where a molar mass, a root mean square (rms) radius, a hydronamic radius and an intrinsic viscosity of particles of the system were defined. Furthermore the interactions were studied by calorimetric measurement ITC, where thermodynamic character of complex formation was determined. Additionally, dynamic and electrophoretic light scattering methods (DLS and ELS) were applied, where hydrodynamic radius and a value of the zeta potential were defined. Also the effect of higher temperature on the character and complex formation was examined by SEC-MALLS and ITC measurements. The interactions were confirmed at any of the used media, but with different efficiency. It was also proved that complexes become smaller in their radii and viscosity with growing BSA concentration. Furthermore it was proved, that the high ionic strength hinders surface charges of HA and BSA molecules and minimizes their mutual interactions. At the higher ionic strength the radii of the complexes, their intrinsic viscosity and zeta potential are increased. The higher temperature has only minimal effect on the formation of the complexes.
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Thermal degradation of hyaluronan
Šimáčková, Marcela ; David, Jan (referee) ; Chytil, Martin (advisor)
This diploma thesis investigated thermal stability and the degradation of hyaluronan (HA) in HA with a molecular mass of 90–130 kDa and in HA with a molecular mass of 1 500–1 750 kDa. The following methods were used for the research: rheology, SEC-MALLS, TGA and DSC. Low-molecular HA was subject to time dependency of degradation investigation, where it was dried at a temperature of 90 °C for a period of 30 minutes and 60 minutes prior to the preparation of the solutions itself. High-molecular HA was investigated not only from the point of view of time but from the point of view of temperature dependency of degradation as well. In the case of investigating the time dependency of degradation, high-molecular HA was dried at a temperature of 75 °C at a time range from 15 minutes to 120 minutes prior to the preparation of the solutions. During the preparation of the solutions for discovering the temperature dependency of degradation, the high-molecular HA was then dried for a period of 30 minutes at a temperature range from 60 °C to 90 °C. For low-molecular HA, thermal stability was proven. Therefore, there is no decrease in the molecular mass and the solutions did not demonstrate a significant decrease of viscosity. For high-molecular HA, thermal stability was not proven. Degradation due to the temperature of drying as well as the time of drying occurred, which was demonstrated by a significant decrease in molecular mass and viscosity of the solutions. While in the case of using a drying temperature of 60 °C, a decrease in the molecular mass occurred by approximately 5 %, the molecular mass decreased by approximately 20 % at a drying temperature of 90 °C compared to undried HA. Due to this reason, high-molecular HA was also further investigated by means of the TGA method, where the decrease of humidity of HA samples in relation to the drying temperature was observed. The DSC method was also used. The objective of the DSC method was to find out temperatures, at which evaporation of humidity contained in an HA sample in relation to its form (undried HA, dried HA and lyophilized HA) occurs. This method further finds out the heat necessary to evaporate humidity from an HA sample. To conclude this research, the results obtained for high-molecular HA were compared with the results of other drying processes – lyophilized proved to be a very gentle drying method because a decrease in the molecular mass for lyophilized HA compared with undried HA almost did not occur.
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Investigation of intercalation of alkaline metals in electrochromic devices
Kortyš, Petr ; Špičák, Petr (referee) ; Svoboda, Vít (advisor)
This work deals with investigation of intercalation of alkaline metals in electrochromic devices by the help of the quartz crystal microbalance method. The general aim is to investigate the influence of molar mass and resistance on properties of vanadium pentoxide and tungsten trioxide electrochromic films. The main measuring method used for investigating of interacalation of sodium and lithium ions into these films is the cyclic voltammetry. Drawn graphs reveals that sodium and lithium ions shows different qualities during intercalation, particularly in participation of solvent, therefore, in the influence of molar mass and in structural changes in the films.
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CHARACTERIZATION OF METALLOCENE-MADE POLYPROPYLENE WITH NARROW DISTRIBUTION OF MOLECULAR WEIGHT
Fojtlová, Lucie ; Poláček, Petr (referee) ; Bálková, Radka (advisor)
Metallocene based polypropylene (mPP) with very narrow distribution of molecular weight was peroxide-degraded to materials of four different molecular weights including the original mPP labeled MET1–MET3 and MET0, respectively. Double bonds formed after peroxide-degradation was proved on material surfaces by FTIR-ATR (attenuated total reflection of Fourier-transformed infrared spectroscopy). The decreasing molecular weight led to gradual decrease of the tensile strength, tensile modulus as well as the strain and to the decrease of the temperature of thermal decomposition. Confocal laser scanning microscopy (CLSM) of chemically etched surfaces of MET0–MET3 revealed supramolecular structure of commonly occurred structure (radical spherulites) but also supramolecular structure of form (sheaf-like structure). The latter was proved by XRD together with the fact that the content of form decreases with decreasing molecular weight. The mentioned structure differences were not visible on DSC curves because the amount of structure was small and melting temperature, temperature of crystallization and the degree of crystallinity remained the same for all four types of mPP. The structure of the original materials was also characterized after isothermal crystallization performed on differential scanning calorimetry (DSC) and under polarizing optical microscope (POM). The first was performed at 120–126 °C and the latter at 130 °C (Tic). The materials obtained on DSC always contained the structure and its amount increased with increasing Tic whereas higher content of form was always in MET0 with respect to MET3. The structure was proved by XRD and also by DSC heating run followed immediately after the isothermal process. The latter revealed two endotherms belonging to melting of and forms. The presence of form was on the surfaces proved by CLSM. The formation of structure was in-situ observed on POM and the amount of it decreased with decreasing molecular weight. The spherulite growth rate increased with decreasing molecular weight whereas the rate of crystalline portion expressed as half-time of crystallization decreased with decreasing molecular weight.
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The influence of molecular weight of polypropylene on isothermal crystallization of nanocomposites
Krajčik, Ladislav ; Poláček, Petr (referee) ; Bálková, Radka (advisor)
This work deals with the study of the influence of metallocene type polypropylene (mPP) molecular weight on isothermal crystallization of its nanocomposites filled with hydrophobic and hydrophilic nanosilica (1 and 2 vol.%). Real amount of nanosilica was determined by thermogravimetry. Isothermal crystallization was performed on differential scanning calorimeter (DSC) at 119–125 °C and observed in-situ under optical polarizing microscope (POM) at 128 °C using hot stage. The increase of mPP crystallinity degree in time was determined on DSC and spherulite type and growth rate was determined using POM. Supramolecular surface structure of the original and isothermally crystallited nanocomposites was observed directly or after chemical etching (mixture of mineral acids with KMnO4) on confocal laser scanning microscope. The crystal structure of mPP was in all tested materials verified by X-ray diffraction.
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Physical ageing of polypropylene
Weiss, Jiří ; Kučera, Jaroslav (referee) ; Tocháček, Jiří (advisor)
Physical aging of commercially produced polypropylene homopolymers Mosten was studied. The work is focused on monitoring the changes in physical properties of polymer in the time period 90 days from the date of preparation of the test specimen. The aging of polymers was realized at storage temperatures of 23 and 80 °C. The changes in crystallinity, yield strength, modulus, elongation and impact strength using DSC method, tensile tests and impact tests according to Charpy were monitored. Molecular weight distribution was determined by means of GPC at each polymer. Relationships between the changes in physical properties and polymer molecular weight were sought.
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SEC-MALLS study on hyaluronan-albumin interactions
Sereda, Alena ; Kalina, Michal (referee) ; Chytil, Martin (advisor)
This work is focused on interactions of hyaluronan (HA) and bovine serum albumin (BSA). These interactions were studied by SEC-MALLS method, where molar mass, root mean square (rms) radii, hydronamic radius and intrinsic viscosity of particles of the system were defined. Additionally, interactions were examined by measurement of DLS and zeta potential, where hydrodynamic radius and a value of the zeta potential were defined. The interactions were confirmed at any of the used media, but with different efficiency. Furthermore it was found out, that the high ionic strength minimizes the range of the interactions, magnifies the radii of the complexes, their intrinsic viscosity and zeta potential. It was proved that complexes become smaller in their radii and viscosity with growing BSA concentraton.
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The Study of Biopolymers Stability Using Light Scattering Techniques
Kratochvíl, Zdeněk ; Sedláček, Petr (referee) ; Kalina, Michal (advisor)
The stability of chosen biopolymers (or simple carbohydrates and amino acids) was in-vestigated using light scattering methods. Samples were prepared by dissolving the sub-stance in deionised water or in diluted acetic acid. Firstly, the effect of increasing concen-tration on zeta potential was observed and the optimal concentration for the next measure-ments was determined. Afterwards, the stability and the molecular weight of used sub-stances were studied during long-time storage in different time intervals. It was found out that chitosan, CMC, hyaluronate and sodium alginate were subjected to degradation whereas increase of the molecular weight and the zeta potential was observed in case of BSA. In the end, the samples were exposed to several different external effects, namely the influence of different temperatures, UV radiation and increasing ionic strength. The results showed that rather higher temperature has a significant impact on biopolymers stability. However, used biopolymers were hardly affected by UV radiation except BSA whose molecular weight increased considerably. Decrease of the zeta potential absolute values and the molecular size usually occurred with increasing ionic strength. The change of molecular weight was not detected.
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