Phd Degree / Doktora
Permanent URI for this collectionhttps://hdl.handle.net/11147/2869
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Doctoral Thesis Development of Conducting Polymer-Based Fluorescence On/Off Biosensor for Biomolecule Analysis(01. Izmir Institute of Technology, 2022) Arslantaş, Duygu; Arslan Yıldız, AhuSensitive and selective detection of biomolecules and cells is essential for early diagnosis of diseases, prognosis monitoring, and effective therapy. This thesis aimed to develop a novel fluorescence ‘‘turn-on/off’’ biosensor for biomolecules and cells detection. In this study, cationic polythiophene derivative poly(1,4-dimethyl-1-(3-((4- methylthiophen-3-yl)oxy)propyl)piperazin-1-ium bromide) (PT–Pip) was used as an efficient fluorescence transduction element to discriminate proteins, mammalian cells, and amino acids for the first time. Initially, pH–dependent spectroscopic characterization of the PT–Pip was performed to monitor the conformational and optical changes. The pH sensitivity of the PT–Pip was demonstrated for the first time. Afterwards, the fluorescence ‘‘turn–off’’ phenomena were investigated in detail using citrate–capped gold nanoparticles as an efficient fluorescence quencher. Further, the interaction of target analytes such as proteins, mammalian cells, and amino acids with pre–quenched non–covalent PT–Pip–AuNP complexes was examined. Disruption of the binding equilibrium between PT–Pip and AuNP by analytes resulted in the selective displacement of PT–Pip, which generated signal output as a fluorescence ‘‘turn–on’’ mode. Consequently, for the sensitive detection of biomolecules and cells, chemical tongue sensor arrays were developed utilizing differential sensing approaches. PCA was used for the statistical evaluation of the multi–dimentional fluorescence response patterns. As a result, unique fingerprints were rapidly obtained by the direct sensing of proteins, ratiometric sensing of mammalian cells, and indirect sensing of amino acids. The combination of a differential sensing strategy with an appropriate multivariate statistical technique enabled the selective and sensitive detection and identification of proteins, mammalian cells, and amino acids.Doctoral Thesis Development and Use of Contactless Magnetic Manipulation Methodologies for the Formation of 3d Cardiac Models(01. Izmir Institute of Technology, 2022) Önbaş, Rabia; Arslan Yıldız, AhuIn this thesis, two contactless magnetic manipulation methodologies were introduced, which are magnetic levitation (MagLev) and biopatterning techniques. The optimization steps of both techniques were completed with NIH/3T3 mouse fibroblast cells. Later, 3D cardiac models were developed using H9c2 rat cardiomyocytes. For the MagLev technique, tunable 3D spheroids were obtained with changing initial cell seeding number, gadobutrol concentrations, and culturing time. For the biopatterning approach, a new bio-ink formulation, which comprises alginate, magnetic nanoparticles, and cells, was developed. Further, biopatterned cellular structures were fabricated in different shapes such as discs, rings, and rectangles under an external magnetic field. Later, characterization was done successfully via immunostaining of collagen I, F-actin, and DAPI. Moreover, cardiac-specific markers; cardiac troponin T and MYH6 were analyzed for both 3D cardiac spheroids and patterned 3D cardiac structures. Finally, doxorubicin was applied to evaluate the drug responses. IC50 values were calculated as 14.7 μM and 8.1 μM for 3D cardiac spheroids and 3D cellular structures respectively, while standard 2D cell culture was 3.5 μM which indicated 3D cardiac models were more resistant to drug exposure. In the last part of thesis, patterned 3D cardiac structures were fabricated using co-cultured hiPSC-derived cardiomyocytes and cardiac fibroblast cells via biopatterning methodology. Characterization was carried out successfully by immunostaining of α-actinin, collagen I, Cx-43, Troponin T, and DAPI. Taken together, to fabricate 3D cell culture models, MagLev and biopatterning-based contactless manipulation methodologies may be good alternatives to conventional 2D cell culture methods for tissue engineering applications, especially for drug screening.