Master Degree / Yüksek Lisans Tezleri
Permanent URI for this collectionhttps://hdl.handle.net/11147/3008
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Master Thesis The Effect of Surface Modification of Biomaterials on the Cellular Interactions(Izmir Institute of Technology, 2008) Özgür, Melek; Çiftçioğlu, MuhsinThe preparation and characterization of chitosan-hydroxyapatite composite scaffolds and protein adsorption chracteristics of these scaffolds have been investigated in this study. The effects of different chitosan/hydroxyapatite contents of the low density composites on the protein adsorption behaviour were experimentally examined.Bradford method at 595 nm and 280 nm UV protein absorption methods were used for the determination of adsorbed amount of bovine serum albumin (BSA) and human serum protein (HSP). In this study low molecular weight chitosan and hydroxyapatite have been used for the preparation of the scaffold composites by freeze drying and SEM was used for microstructural analysis. The thermal behaviour of the composites was investigated by DSC and TGA. Composite scaffolds were prepared by using different amounts of chitosan and hydroxyapatite (HA) and six different scaffolds were prepared and coded as C100H0, C80H20, C70H30, C50H50, C30H70, and C20H80. The porous low density scaffolds had 93.5-96.3% porosity with a slight increase in density with increasing HA content. The interconnected pore network was formed from 50-250 .m relatively uniform size pores with thin pore walls. The HA particles were fully embedded in the polymer matrix in the pore walls. The TGA curves have shown that the freeze dried phase seperation induced biopolymer sturucture degrates at lower temperatures faster than the original raw polymer. The adsorptions of BSA and HSP onto composites have been studied as a function of time, protein concentration and pH. Adsorption experiments were also conducted with commercial HA powder. The adsorption kinetics experiments have indicated that protein adsorption was almost completely achieved in the first 2-3 hours with relatively high uptake values of up to 45-60 mg/g and 40-60 mg/g for 595 nm Bradford and 280 nm methods. The adsorption behaviour did not fit to the commonly known Langmuir and Freundlich isotherms. This was attributed to the swelling/degradation tendency of the freeze-dried chitosan containing scaffolds. The HSP uptake of 30 and 50 wt% HA containing composites were in the 50-60 mg/g range which was higher than other composites and the raw unprocessed chitosan.Master Thesis Preparation and Characterization of Chitosan/Calcium Phosphate Based Composite Biomaterials(Izmir Institute of Technology, 2004) Yıldırım, Oktay; Çiftçioğlu, MuhsinIn this study the preparation and characterization of three-dimensional chitosan-calcium phosphate composite structures and porous hydroxyapatite bodies for biomaterial applications have been studied. The effects of chitosan calcium phosphate amount on density, porosity, microstructure, chemical composition and mechanical properties on the composites and effects of porosifier contents, hydroxyapatite content of the slurry and sintering temperature on density, porosity and microstructure of the porous ceramic samples were investigated. SEM was used for microstructural analysis, XRD and FTIR were used for chemical analysis, Archimedes method was used for investigating physical properties and compression test for investigating mechanical properties. In this study low molecular weight chitosan, -tricalciumphosphate, hydroxyapatite and hydroxyapatite whisker have been used. For composites freeze drying technique and for the porous bodies dry pressing, polymer sponge method and dough method have been used.The densities of the composites prepared by using chitosan as the matrix and hydroxyapatite, hydroxyapatite whisker, and B-tricalciumphosphate as reinforcement increased and the porosities decreased with the increase in the ceramic content. The modulus of elasticity and the yield stress generally increased with the increasing ceramic content except for the chitosan/-tricalciumphosphate composites. The densities and porosities of the composite structures varied in the range of 0.059-0.29 g/cm3 and 96-88% respectively. The elastic moduli of the composites varied in a range of 4.45-10.09 MPa and yield stress varied in a range of 0.14-0.34 Mpa due to the change in the ceramic weight%. Changing the ceramic weight% also had influence on the microstructure. Generally with increasing ceramic content the pore sizes decreased.The pore sizes varied in a range between 100-250, 100-400 and 100-200 for chitosan/hydroxapatite, Chitosan/-TCP/Hydroxyapatite and chitosan/HA whisker composites respectively. FTIR and XRD analysis showed that the composite structures contained original constituents, no new chemical compounds were formed the production process had not affected crystallinity of ceramic phases. The densities of the porous ceramic bodies decreased and the porosities increased with the increasing porosifier content at the porous ceramics prepared by dough method and dry pressing method. The porosity and density values of porous hydroxyapatite samples changed in range of 34-72% and 2.03 to 0.87 g/cm3. Pore sizes of polymeric sponge samples were found to be around 300-400 and dry pressing and dough method samples were found to be 10u.