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Modification of hyaluronan by cholic acid and the using of these derivatives for carrier applications
Kvaková, Klaudia ; Márová, Ivana (referee) ; Velebný, Vladimír (advisor)
Amphiphilic biopolymers were synthesised using esterification of hyaluronic acid (HA) and cholic acid as hydrophobic segment. First, step of synthesis involves the activation of cholic acid carboxylic moiety by reaction with benzoylchloride and triethylamine (TEA) using as solvent tetrahydrofuran (THF). The formed mixed aliphatic/aromatic anhydride (intermediate) reacted at room temperature with hyaluronic acid catalysed by 4-(dimethylamino)pyridine (DMAP) and triethylamine and using as solvent water/THF. Hydrophobized product was identified as sodium cholyl hyaluronate (HA-CA) was obtained as product of the reaction. Structure of derivative was characterised by Nuclear magnetic resonance (NMR) and Fourier Transform - Infrared Spectroscopy (FT-IR). Size exclusion chromatography (SEC-MALLS) was used to determine molecular weight of derivative to evaluate any possible degradation of hyaluronan during modification. Rheological properties of these substances were also examined and confirmed non-degradation. The hydrophobized hyaluronic acid properties were evaluated for application as drug delivery system. Therefore, two non-polar compounds were encapsulated (coenzyme Q10 and curcumin). The size of formed polymeric micelles was characterised by dynamic light scattering (DLS).
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Hyaluronan-Micelle Aggregates and their Potential for Nanomedicine Applications
Pilgrová, Tereza ; Burgert, Ladislav (referee) ; Reháková, Milena (referee) ; Pekař, Miloslav (advisor)
This thesis deals with the study of preparation and characterization of hyaluronan-micelle aggregates. The theoretical part deals with drug delivery systems, characterization of used materials and methods especially fluorescence spectroscopy, dynamic light scattering and turbidimetry. Methods of determination of measured data are summarized in the experimental section. The result section is divided into two subsections dedicated to different preparation methods of hyaluronan-surfactant complexes. Induced aggregates of hyaluronan with Septonex are characterized in terms of their origin and stability, and the results are compared with previously studied surfactants CTAB. In the second part are discussed so-called decorated micelles, their formation, properties and stability.
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Stability of controlled drug release systems based on plasticized starch
Zhukouskaya, Hanna ; Štěpánek, Miroslav (advisor) ; Hrubý, Martin (referee)
The thesis is focused on the research of stability of controlled drug release systems based on a blend of plasticized starch/polycaprolactone (TPS/PCL) that served as a carrier. Antibiotic vancomycin was used as a model drug, and its release from TPS/PCL pellets into aqueous environment was followed by UV-spectroscopy and the obtained time dependences were treated by a simple kinetic model. Moreover, the simultaneous release of starch particles to the surrounding liquid phase was studied by static and dynamic light scattering as well as transmission electron microscopy (TEM) in order to obtain information on the stability of biodegradable matrix and on the structure of the products of the pellet decomposition on a nanoscale level. Key words: vancomycin, starch, drug delivery system, polycaprolactone (PCL), particle release, dynamic light scattering (DLS), static light scattering (SLS)
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Amphiphilic Dendritic Compounds as Drug Delivery Systems.
Edr, Antonín
To enable an easy detection of supramolecular objects assembled from 1 or 2, I am currently working on preparation of their unsymmetrical analogues 3 and 4 bearing a fluorescent tag. Final liposomes or micelles will be prepared from mixtures of fluorescent and nonfluorescent analogues.\n
Fulltext: content.csg -  PDF
Plný tet: SKMBT_C22019053108333 - PDF
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Hyaluronan-Micelle Aggregates and their Potential for Nanomedicine Applications
Pilgrová, Tereza ; Burgert, Ladislav (referee) ; Reháková, Milena (referee) ; Pekař, Miloslav (advisor)
This thesis deals with the study of preparation and characterization of hyaluronan-micelle aggregates. The theoretical part deals with drug delivery systems, characterization of used materials and methods especially fluorescence spectroscopy, dynamic light scattering and turbidimetry. Methods of determination of measured data are summarized in the experimental section. The result section is divided into two subsections dedicated to different preparation methods of hyaluronan-surfactant complexes. Induced aggregates of hyaluronan with Septonex are characterized in terms of their origin and stability, and the results are compared with previously studied surfactants CTAB. In the second part are discussed so-called decorated micelles, their formation, properties and stability.
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Modification of hyaluronan by cholic acid and the using of these derivatives for carrier applications
Kvaková, Klaudia ; Márová, Ivana (referee) ; Velebný, Vladimír (advisor)
Amphiphilic biopolymers were synthesised using esterification of hyaluronic acid (HA) and cholic acid as hydrophobic segment. First, step of synthesis involves the activation of cholic acid carboxylic moiety by reaction with benzoylchloride and triethylamine (TEA) using as solvent tetrahydrofuran (THF). The formed mixed aliphatic/aromatic anhydride (intermediate) reacted at room temperature with hyaluronic acid catalysed by 4-(dimethylamino)pyridine (DMAP) and triethylamine and using as solvent water/THF. Hydrophobized product was identified as sodium cholyl hyaluronate (HA-CA) was obtained as product of the reaction. Structure of derivative was characterised by Nuclear magnetic resonance (NMR) and Fourier Transform - Infrared Spectroscopy (FT-IR). Size exclusion chromatography (SEC-MALLS) was used to determine molecular weight of derivative to evaluate any possible degradation of hyaluronan during modification. Rheological properties of these substances were also examined and confirmed non-degradation. The hydrophobized hyaluronic acid properties were evaluated for application as drug delivery system. Therefore, two non-polar compounds were encapsulated (coenzyme Q10 and curcumin). The size of formed polymeric micelles was characterised by dynamic light scattering (DLS).
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