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Characterization of coloid particles by excited-state proton transfer with advanced fluorescence techniques
Kotouček, Jan ; Mravec, Filip (referee) ; Pekař, Miloslav (advisor)
The deprotonation characteristics of fluorescent probes -naphthol and 8-hydroxypyrene-1,3,6-trisulphonic acid (HPTS) were studied in this diploma thesis, using steady-state and time-resolved fluorescence spectroscopy. Two cationic surfactants, Septonex and cetyltrimethylammonium bromide (CTAB), were studied. These surfactants were measured in the complex with hyaluronan (1.75 MDa, 1 MDa and 300 kDa). Steady-state fluorescence was used for determination of critical aggregation concentration of each surfactant and pKa*. Time-resolved fluorescence decays were used to calculate the average lifetimes and the deprotonation constants of naphthol and HPTS. The measurement with hyaluronan were compared with the polystyrenesulfonate (PSS) – surfactant system. The effect of hydration shell of hyaluronan on hyaluronan – surfactant complex formation results from the comparison of above mentioned systems. Large differences were found in the deprotonation characteristic between surfactants and even between individual molecular weights of hyaluronan. The measurement shows that the hydration shell is located near to the dissociated carboxyl groups of hyaluronan chain, where the interaction with the positively charged surfactants occurs. Furthermore, the aggregation number of Septonex was determined by quenching of pyrene using cetylpyridinium chloride (CPC) as a quencher. The aggregation number for 20 mM Septonex solution was determined as a value of 104 molecules. CPC was used for confirmation of the localization of -naphthol in the micelles of CTAB and polymer – CTAB, respectively.
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Study of the hydration shell of vesicular systems based on ionic amphiphilic pairs
Rašticová, Barbora ; Szabová, Jana (referee) ; Mravec, Filip (advisor)
This bachelor thesis deals with the study of hydration shell of positively charged vesicular systems. The aim of the work was to monitor the hydration shell and to find out the amount of water molecules in the environment at different conditions of the membrane. Furthermore, a comparison of two selected fluorescent probes were studied. Positively charged vesicular systems composed of two types of surfactants were used, namely negatively charged SDS and positively charged CTAB. The two-chain positively charged surfactant was also added, resulting a positively charged vesicular systems. Three different concentrations of cholesterol were selected for the study and added to the system, namely 20, 40 and 60 mol. %. The study was performed by measuring the fluorescent emission as a function of temperature. The temperature range was from 10 to 80 °C. As a fluorescent probe Laurdan and Prodan were selected. For evaluation the method of generalized polarization was used. Due to its structure, Laurdan is mainly found in the membrane environment, so the method of two-wavelength generalized polarization, which includes fluorescence contributions only from the membrane, was sufficient for its evaluation. Compared to Laurdan, Prodan has a shorter hydrocarbon chain, so its distribution is not only in the membrane but also in the aqueous environment. Therefore, the method of three-wavelength generalized polarization, which also includes the contribution of fluorescence from the aqueous environment was used. The results showed that the behaviour of both probes is very similar. In all systems, the values of generalized polarization decreased with increasing temperature. Thus, at low temperatures, the membrane is in a solid ordered phase. With increasing temperature, it transforms into a liquid disordered phase. Thus, with increasing temperature, the number of water molecules increases. As the cholesterol concentration increased, the phase transition interval increased. The results also showed that the values of Prodan’s three wavelength generalized polarization are always higher than the values of Laurdan’s two wavelength generalized polarization.
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Study of the hydration shell of vesicular systems based on ionic amphiphilic pairs
Rašticová, Barbora ; Szabová, Jana (referee) ; Mravec, Filip (advisor)
This bachelor thesis deals with the study of hydration shell of positively charged vesicular systems. The aim of the work was to monitor the hydration shell and to find out the amount of water molecules in the environment at different conditions of the membrane. Furthermore, a comparison of two selected fluorescent probes were studied. Positively charged vesicular systems composed of two types of surfactants were used, namely negatively charged SDS and positively charged CTAB. The two-chain positively charged surfactant was also added, resulting a positively charged vesicular systems. Three different concentrations of cholesterol were selected for the study and added to the system, namely 20, 40 and 60 mol. %. The study was performed by measuring the fluorescent emission as a function of temperature. The temperature range was from 10 to 80 °C. As a fluorescent probe Laurdan and Prodan were selected. For evaluation the method of generalized polarization was used. Due to its structure, Laurdan is mainly found in the membrane environment, so the method of two-wavelength generalized polarization, which includes fluorescence contributions only from the membrane, was sufficient for its evaluation. Compared to Laurdan, Prodan has a shorter hydrocarbon chain, so its distribution is not only in the membrane but also in the aqueous environment. Therefore, the method of three-wavelength generalized polarization, which also includes the contribution of fluorescence from the aqueous environment was used. The results showed that the behaviour of both probes is very similar. In all systems, the values of generalized polarization decreased with increasing temperature. Thus, at low temperatures, the membrane is in a solid ordered phase. With increasing temperature, it transforms into a liquid disordered phase. Thus, with increasing temperature, the number of water molecules increases. As the cholesterol concentration increased, the phase transition interval increased. The results also showed that the values of Prodan’s three wavelength generalized polarization are always higher than the values of Laurdan’s two wavelength generalized polarization.
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Characterization of coloid particles by excited-state proton transfer with advanced fluorescence techniques
Kotouček, Jan ; Mravec, Filip (referee) ; Pekař, Miloslav (advisor)
The deprotonation characteristics of fluorescent probes -naphthol and 8-hydroxypyrene-1,3,6-trisulphonic acid (HPTS) were studied in this diploma thesis, using steady-state and time-resolved fluorescence spectroscopy. Two cationic surfactants, Septonex and cetyltrimethylammonium bromide (CTAB), were studied. These surfactants were measured in the complex with hyaluronan (1.75 MDa, 1 MDa and 300 kDa). Steady-state fluorescence was used for determination of critical aggregation concentration of each surfactant and pKa*. Time-resolved fluorescence decays were used to calculate the average lifetimes and the deprotonation constants of naphthol and HPTS. The measurement with hyaluronan were compared with the polystyrenesulfonate (PSS) – surfactant system. The effect of hydration shell of hyaluronan on hyaluronan – surfactant complex formation results from the comparison of above mentioned systems. Large differences were found in the deprotonation characteristic between surfactants and even between individual molecular weights of hyaluronan. The measurement shows that the hydration shell is located near to the dissociated carboxyl groups of hyaluronan chain, where the interaction with the positively charged surfactants occurs. Furthermore, the aggregation number of Septonex was determined by quenching of pyrene using cetylpyridinium chloride (CPC) as a quencher. The aggregation number for 20 mM Septonex solution was determined as a value of 104 molecules. CPC was used for confirmation of the localization of -naphthol in the micelles of CTAB and polymer – CTAB, respectively.
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