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, Muhsin
    The 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 Hydroxyopatite and Polymer Composite Biomaterials
    (Izmir Institute of Technology, 2002) Gültekin, Naz; Tıhmınlıoğlu, Funda
    In the thesis, the preparation and characterization of polylactide-Hydroxyapatite(HA) composite films for biomaterial applications have been studied. The effects of number of parameters such as polymer type, HA loading, surface modification and its concentration on the mechanical, thermal microstructural and hydrolytic degradation properties of the composites were investigated. Four different types of polymers, Poly (L-lactide)(PLA1), 96/4 L-lactide,D-Lactide Copolymer (PDLA1), Poly (L-Lactide)(PLA2), and 67/23 Poly (L-Lactide-co-D,L-Lactide)(PDLA2), have been used. In this study, PolyLactide-HA composite films have been prepared by solvent-casting technique. The HA powder was synthesized by precipitation technique. Interfacial interactions between HA and polylactide polymer were modified to improve filler compatibility and mechanical properties of the composites by surface treatment of the HA with two different silane coupling agents; 3-aminopropyltriethoxysilane (AMPTES) and 3-mercaptopropyltrimethoxysilane (MPTMS) at three different concentration. Silane treatment indicated better dispersion of HA particles in the polymer matrix and improvements in the mechanical properties of the composites compared to the untreated HA loaded polylactide composites. Tensile test results showed that the maximum improvement in the mechanical properties of the composites was obtained for the PLA composites containing 1 wt % aminofunctional silane treated HA and 0.5 wt % mercaptopropyltrimethoxy silane treated HA for PDLA composites. Scanning electron microscopy studies also revealed better dispersion of silane treated HA particles in the polymer matrix. Thermal degradation kinetics of the composites was investigated and it was found that addition of HA into polymer matrix decreased the thermal degradation temperature and also slowed down the degradation rate. In this study, the hydrolytic degradation of poly (L-Lactide)(PLA), poly (L-Lactide-co-D-Lactide) (PDLA) and their hydroxyapatite (HA) loaded composites (10-50-w/w %) were investigated in simulated body fluid (SBF) at 37 0C and at pH 7.4 by in vitro static testing. Using different techniques, namely weighting to quantify water absorption monitored the hydrolytic degradation and weight loss, scanning electron microscopy (SEM) to observe morphological changes occurred at the surface of the films over time. At the end of the 150 days, only 12.5 wt % and 9.5 wt % of weight PLA1 and PLA2 were lost respectively. Degradation of the copolymers was faster than PLA1 and PLA2 and weight loss data of PDLA1 and PDLA2 were found to be nearly same with 17.5 wt % and 17 wt %, respectively. The changes of pH on all polymer were stable at 7.4, because of simulated body fluid indicates buffer solution properties. Degradation rate of PLA and PDLA composites containing 10 wt % HA decreased, and also water absorption of these samples increased. Weight loss decreased approximately from 12 wt % to 5 wt % and water absorption increased from 10 wt % to 13 wt % for PLA composites containing 10 wt % HA. The change of microstructural properties of obtained composites has been determined in simulated body fluid as a function of time. It was found that the surface of polymer composite films was coated with the calcium phosphate layer. This coating was increased with HA loading and ageing time.