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Hyaluronic gels for control release of active substances
Hekrlová, Veronika ; Smilek, Jiří (referee) ; Klučáková, Martina (advisor)
This diploma thesis is focused on the development of materials based on oxidized hyaluronic acid derivative (HA-Ox) crosslinked using bifunctional alkoxyamine POA. Hydrogels have been studied as potential matrices for the controlled release of biological drugs. For this purpose, hydrogels containing bovine serum albumin (BSA) as model of the active substances were prepared. The properties of the hydrogels were affected by the concentration of the derivative (10 mg / ml, 20 mg / ml and 30 mg / ml). In the first part of the work, the viscoelastic properties, swelling and dry matter content of the prepared hydrogels were evaluated. The dry matter of the starting hyaluronan derivative and the weight of the polymer network in the hydrogels were determined gravimetrically and by TGA (in all cases about 80% w/w). The difference in weight of the polymer contained in the hydrogels before and after swelling showed that the non-crosslinked sol leaches out of the hydrogel during swelling (about 10-20% w/w). Due to this phenomenon, hydrogels with a concentration of 10 mg / ml are depleted of hydrogels, while their more concentrated analogues swell even after the sol has washed off. The sizes of elastic moduli needed to calculate the mesh of the polymer network were determined using rheological measurements (amplitude and frequency test). The mesh size of the polymer network itself is calculated using two commonly used theories: Equilibrium SwellingTheory (EST) and Rubber Elasticity Theory (RET). The mesh size of BSA-free gels with a derivative concentration of 10 to 30 mg/ml was determined according to EST to 347 ± 29 nm, 319 ± 15 nm, 295 ± 6 nm and according to RET345 ± 30 nm, 308 ± 14 nm, 268 ± 5 nm. For hydrogels with BSA, the mesh sizes of the polymer network were determined according to EST 373 ± 34 nm, 307 ± 11 nm, 281 ± 7 nm and according to RET 372 ± 32 nm, 297 ± 11 nm, 258 ± 6 nm. The mesh size of the polymer network decreases with higher derivative concentration. In the second part of the work, the release of the model active substance BSA was monitored spectrophotometrically using fluorescent labeling. Using the Korsmeyer-Peppas model, it was found that diffusion release is the primary mechanism.
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Hyaluronic gels for control release of active substances
Hekrlová, Veronika ; Smilek, Jiří (referee) ; Klučáková, Martina (advisor)
This diploma thesis is focused on the development of materials based on oxidized hyaluronic acid derivative (HA-Ox) crosslinked using bifunctional alkoxyamine POA. Hydrogels have been studied as potential matrices for the controlled release of biological drugs. For this purpose, hydrogels containing bovine serum albumin (BSA) as model of the active substances were prepared. The properties of the hydrogels were affected by the concentration of the derivative (10 mg / ml, 20 mg / ml and 30 mg / ml). In the first part of the work, the viscoelastic properties, swelling and dry matter content of the prepared hydrogels were evaluated. The dry matter of the starting hyaluronan derivative and the weight of the polymer network in the hydrogels were determined gravimetrically and by TGA (in all cases about 80% w/w). The difference in weight of the polymer contained in the hydrogels before and after swelling showed that the non-crosslinked sol leaches out of the hydrogel during swelling (about 10-20% w/w). Due to this phenomenon, hydrogels with a concentration of 10 mg / ml are depleted of hydrogels, while their more concentrated analogues swell even after the sol has washed off. The sizes of elastic moduli needed to calculate the mesh of the polymer network were determined using rheological measurements (amplitude and frequency test). The mesh size of the polymer network itself is calculated using two commonly used theories: Equilibrium SwellingTheory (EST) and Rubber Elasticity Theory (RET). The mesh size of BSA-free gels with a derivative concentration of 10 to 30 mg/ml was determined according to EST to 347 ± 29 nm, 319 ± 15 nm, 295 ± 6 nm and according to RET345 ± 30 nm, 308 ± 14 nm, 268 ± 5 nm. For hydrogels with BSA, the mesh sizes of the polymer network were determined according to EST 373 ± 34 nm, 307 ± 11 nm, 281 ± 7 nm and according to RET 372 ± 32 nm, 297 ± 11 nm, 258 ± 6 nm. The mesh size of the polymer network decreases with higher derivative concentration. In the second part of the work, the release of the model active substance BSA was monitored spectrophotometrically using fluorescent labeling. Using the Korsmeyer-Peppas model, it was found that diffusion release is the primary mechanism.
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