Phd Degree / Doktora
Permanent URI for this collectionhttps://hdl.handle.net/11147/2869
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Doctoral Thesis Development of Chitosan Based Biofoams(Izmir Institute of Technology, 2020) Olcay Kurt, Aybike Nil; Polat, Mehmet; Polat, Hürriyet; Polat, Mehmet; Polat, HürriyetChitosan is a preferred bio-foam material used in many research fields such as tissue engineering and drug delivery due to its unique structural features (wide pH stability, nontoxic-biocompatible-biodegradable, anti-inflammatory, antimicrobial). However, chitosan foams are mechanically too weak to maintain the desired shape until newly formed tissue natures. A wound infection and serious tissue necrosis, endanger human's lives. So, a dressing is required to protect loss of fluids and proteins from the wound area and prevents any bacterial invasion replacing the function of skin temporarily. Therefore controlled drug release from a wound dressing is necessary with a biocompatibility and enough mechanical strength. The aim of this study was the synthesis of mechanically durable - dual porosity chitosan bio-foams to provide a controlled drug release. For this purpose, oil droplets formed in a chitosan solution were used as templates to produce micropores that also contain vancomycin (a model antibiotic-hydrophylic) and curcumin (a model anti-inflammatory-hydrophobic) in the walls of the chitosan matrix with large structural voids. An anionic surfactant, sodium dodecyl sulfate (SDS) alone, was used as a crosslinking agent which was a new approach. Then the structures were characterized by SEM, FTIR, mechanical tests and BET analysis. The chitosan foams have dual pore structures. 1) The intrinsic micro pores that the walls of chitosan matrix have with different morphology that depends on the oil phase. 2) The structural voids that the chitosan matrix have, present even in the absence of an oil phase that depends on the experimental conditions. The mechanical strength of the foams were found to be much higher (up to 250 kPa) compare to the foams produced in literature and suggested to be suitable to use for wound dressing applications. The drug release mechanism of foams were found to depend on the conditions used for foam development and the released kinetics were presented with a mathematical model.Doctoral Thesis Natural and Synthetic Silica Incorporated Chitosan Composite Scaffolds for Bone Tissue Engineering Applications(İzmir Institute of Technology, 2016) Tamburacı, Sedef; Tıhmınlıoğlu, Funda; Tıhmınlıoğlu, Funda; Havıtçıoğlu, HasanRecently bone tissue engineering studies have focused on the development of 3D scaffolds that can organize the tissue regeneration in natural way with appropriate porosity and reinforced the structure. Natural polymer-based composites have been focused with more attention than synthetic polymer composites for bone tissue engineering applications because of their biocompatibility and biodegradability. In this work, the goal was to combine the useful biomaterial properties of both chitosan and silica to design biocomposite organic/inorganic biomaterials for bone tissue engineering applications. The composite scaffolds were fabricated by freeze drying method bu using two different silicas; natural silica; Diatomite and synthetic silica, octa (tetramethylammonium) polyhedral oligomeric silsesquioxanes (OctaTMA-POSS). The effects of silica type and loading on the mechanical, morphological, chemical, surface properties, wettability and biocompatibility of composite scaffolds were investigated and characterized by using SEM, AFM, contact angle analysis, swelling study, protein adsorption assay, biodegradation and biomineralization tests. WST-1 cytotoxicity, cell proliferation with rezasurin and alkaline phosphatase activity assays were performed to determine biological activity of the composite scaffolds. In vitro biomineralization on scaffolds was determined by Von Kossa and Alizarin red staining. POSS and diatomite incorporation increased the surface roughness. Chitosansilica composites exhibited 82-90% porosity. Wet chitosan-silica composite scaffolds exhibited higher compression moduli compared to pure chitosan scaffold in 67.3- 81.4kPa and 78.1 to 107.6kPa range respectively. Average pore size range of chitosandiatomite and chitosan-POSS composite scaffolds was obtained as 15-180μm and 220- 300μm, respectively. Results indicated that chitosan-silica composites did not show any cytotoxic effect on 3T3, MG-63 and Saos-2 cell lines. Chitosan-silica composites were found to be favorable for osteoblast proliferation. Diatomite and POSS incorporation showed promising effects with enhancing ALP activity on hFob cells. Therefore, these composite scaffolds could be used for bone tissue engineering applications.
