Master Degree / Yüksek Lisans Tezleri
Permanent URI for this collectionhttps://hdl.handle.net/11147/3008
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Master Thesis Synthesis and Characterization of Polycaprolactone-Polyvalerolactone Copolymer and Its Use in Melt Electrowriting Applications(01. Izmir Institute of Technology, 2024) Dinçkal, Sanem; Yıldız, Ümit Hakan; Yıldız, Ümit Hakan; 04.01. Department of Chemistry; 04. Faculty of Science; 01. Izmir Institute of TechnologyThis thesis focuses on the synthesis and characterization of Poly(ε-caprolactone) (PCL) and its block copolymers, Poly(ε-caprolactone)-b-Poly(4-hydroxyvalerate) (PCL-b-P4HV) and Poly(ε-caprolactone)-b-Poly(δ-valerolactone) (PCL-b-PVL). These polymers were synthesized through ring-opening polymerization of various lactones (ε-caprolactone, γ-valerolactone, and δ-valerolactone) using biocatalysts such as citric acid, glycolic acid, salicylic acid, boric acid and acetic acid. Detailed analytical and thermoanalytical characterizations were performed. Differential Scanning Calorimetry (DSC) showed that most homopolymers and copolymers exhibited crystallization (Tc) and melting temperatures (Tm) varying between 5-25°C and 50-65°C respectively, confirming successful polymerization. DSC thermograms of block copolymers revealed that solvent choice for precipitation affected crystallinity and thermal properties, with a small second melting point observed due to different crystalline forms. Fourier Transform Infrared Spectroscopy-Attenuated Total Reflectance (FTIR-ATR) confirmed the homopolymerization of Poly(ε-caprolactone) using citric, glycolic, and salicylic acids. Mass spectrometry further revealed characteristic peaks corresponding to expected molecular weights and compositions of the copolymers. The presence of these peaks corroborated the formation of block copolymers with distinct blocks of PCL, P4HV, and PVL confirmed the molecular integrity of the synthesized block copolymers. This thesis provides a comprehensive analysis of the synthesis and characterization of block copolymers, offering insights into their structural properties and potential applications. The findings contribute to the understanding of the polymerization process and the properties of the resulting materials, which are significant for industrial and biomedical applications. The resultant copolymers were utilized in Melt Electrowriting process to provide tissue scaffold. Despite their brittleness, all copolymers were electrowritten without issues, indicating their potential interest in tissue engineering applications.Master Thesis Surface Modification of Chitosan Films/Meshes for Biomaterial Applications(Izmir Institute of Technology, 2019) Işıklı, Berçin; Tıhmınlıoğlu, Funda; Tıhmınlıoğlu, Funda; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyModification of surface of biomaterials is a great interest for many years due to first contact of surface of materials with the biological fluids. This thesis aims to investigate surface modification effect on the chemical, surface wettability, protein adsorption as well biodegradability properties of dense chitosan (Ch) and asymmetric chitosan films (ACh). The surfaces of chitosan dense and asymmetric films were modified by ion implantation technique using carbon and carbon-nitrogen hybrid ions at a fluence of 1x1015 ions/cm2 and ion energy of 20kV. Chemical compositions of the film surfaces were analyzed by Fourier transform infrared spectroscopy (FTIR-ATR). Surface hydrophobicity measurements were conducted by static contact angle measurements. Protein adsorption on unmodified and modified surfaces on films was investigated as a function of time at various pH conditions. After ion implantation on chitosan films, both C and C-Nitrogen ion implantation, the surfaces become rougher and hydrophobic having moderate wettability (����� values in the range of 72-85°) and in good agreement with FTIR-ATR data findings. It was found pH dependence of the amount of protein adsorbed on the dense chitosan films as a function of time for both un-implanted and implanted films. BSA and fibrinogen were more adsorbed on the chitosan films at pH 5. The amount of BSA and fibrinogen protein adsorption was 0.97 and 1.33 gprotein/gfilm, respectively for 60 min incubation period. Protein adsorption enhanced for C and C+N2 ion implanted samples for BSA and fibrinogen, respectively due to the hydrophobic protein surface interaction effect. In vitro degradation results showed that ACh films degrade much faster (mass loss 57 %) than Ch films (40 %) due to the porous structure at the end of 3 weeks. However, the ion implanted Ch samples degraded much slower having mass loss of 30% and 17.7% for C+N2 and C implanted samples, respectively at the end of 3 weeks compared to un-implanted Ch films as 40 %. The results are in good agreement with water sorption and surface hydrophobicity of the implanted films. This study demonstrated that surface modification, as well as structure, changes the protein sorption, wettability and biodegradation properties of the chitosan films.