A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines

Novel fluorine-18 labelled luminescent rhenium tricarbonyl complexes were synthesised to test their utility as agents for position emission tomography (PET) and optical hybrid imaging. These experiments lead to the discovery of a rhenium complexation-dissociation method, which produced never-before-...

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Main Author: Klenner, Mitchell Ashley
Format: Thesis
Published: Curtin University 2019
Online Access:http://hdl.handle.net/20.500.11937/77107
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author Klenner, Mitchell Ashley
author_facet Klenner, Mitchell Ashley
author_sort Klenner, Mitchell Ashley
building Curtin Institutional Repository
collection Online Access
description Novel fluorine-18 labelled luminescent rhenium tricarbonyl complexes were synthesised to test their utility as agents for position emission tomography (PET) and optical hybrid imaging. These experiments lead to the discovery of a rhenium complexation-dissociation method, which produced never-before-seen radiotracers in substantial radiochemical yields that were unable to be radiosynthesised by traditional means. This method was further applied to the successful production of the Alzheimer’s disease PET imaging nuclear medicine, [18F]CABS13, and new analogues thereof.
first_indexed 2025-11-14T11:09:29Z
format Thesis
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T11:09:29Z
publishDate 2019
publisher Curtin University
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spelling curtin-20.500.11937-771072019-12-05T05:28:26Z A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines Klenner, Mitchell Ashley Novel fluorine-18 labelled luminescent rhenium tricarbonyl complexes were synthesised to test their utility as agents for position emission tomography (PET) and optical hybrid imaging. These experiments lead to the discovery of a rhenium complexation-dissociation method, which produced never-before-seen radiotracers in substantial radiochemical yields that were unable to be radiosynthesised by traditional means. This method was further applied to the successful production of the Alzheimer’s disease PET imaging nuclear medicine, [18F]CABS13, and new analogues thereof. 2019 Thesis http://hdl.handle.net/20.500.11937/77107 Curtin University fulltext
spellingShingle Klenner, Mitchell Ashley
A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines
title A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines
title_full A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines
title_fullStr A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines
title_full_unstemmed A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines
title_short A Novel Radiofluorination Method for the Design of Rhenium(I) PET-Optical Hybrid Nuclear Medicines
title_sort novel radiofluorination method for the design of rhenium(i) pet-optical hybrid nuclear medicines
url http://hdl.handle.net/20.500.11937/77107