Burianova, Valeriia (2025) The synthesis and development of radionuclide based tracers for the imaging of diseases. PhD thesis, University of Glasgow.
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Abstract
This PhD focused on the development of synthetic methods for the preparation of known and novel PET imaging agents targeting the central nervous system. The first project created a second-generation enantioselective synthesis of [18F]SynVesT-1, a PET imaging agent for the synaptic vesicle protein 2A (SV2A), along with its non-radiofluorinated standard. Additionally, a modification of this route allowed the synthesis of the novel radioligand, [3H]SynVesT-1, for SV2A autoradiography.
The next project focused on the synthesis of novel PET imaging agents for the monocarboxylate transporters-1 and -2. A small library of fluorinated and methoxylated 6 substituted thieno[2,3-d]pyrimidinedione-5-carboxamide analogues was synthesised via an eight-step route. The physicochemical properties of the developed compounds were evaluated using HPLC methodology, with all showing favourable characteristics.
The final project was dedicated to the development of novel fluorescent α-amino acids via derivatisation of tryptophan at C2-position through alkenylation (Horner-Wadsworth-Emmons and Witting) and arylation (Suzuki-Miyaura) reactions. The resulting amino acids showed excellent photophysical properties, solvatochromism and pH sensitivity.
Item Type: | Thesis (PhD) |
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Qualification Level: | Doctoral |
Subjects: | Q Science > QD Chemistry |
Colleges/Schools: | College of Science and Engineering > School of Chemistry |
Funder's Name: | Engineering and Physical Sciences Research Council (EPSRC) |
Supervisor's Name: | Sutherland, Professor Andrew |
Date of Award: | 2025 |
Depositing User: | Theses Team |
Unique ID: | glathesis:2025-85384 |
Copyright: | Copyright of this thesis is held by the author. |
Date Deposited: | 13 Aug 2025 07:50 |
Last Modified: | 13 Aug 2025 07:51 |
Thesis DOI: | 10.5525/gla.thesis.85384 |
URI: | https://theses.gla.ac.uk/id/eprint/85384 |
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