Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.633561
Title: Synthetic routes to 18F-labelled gemcitabine and related 2’-fluoronucleosides
Author: Meyer, Jan-Philip
ISNI:       0000 0004 5346 655X
Awarding Body: Cardiff University
Current Institution: Cardiff University
Date of Award: 2015
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Abstract:
Gemcitabine (2’,2’-difluoro-2’-deoxycytidine, dFdC) is an established chemotherapeutic agent used in the treatment of various carcinomas such as lung, breast, bladder and especially pancreatic cancer. However, its general application and bioavailability is compromised due to both poor cell uptake and rapid metabolism by gut and liver cytidine deaminase (CDA). A 18F-gemcitabine positron emission tomography (PET) probe could enable biodistribution studies and the imaging of gemcitabine pharmacodynamics in vivo. However, the potential and clinical relevance of a 18F-gemcitabine PET probe would have to be evaluated using appropriate PET tumour models. In order to approach the synthetic target molecule 18F-dFdC, proof-of-principle studies on more straightforward synthetic targets including 18F-FAU and 18FFAC (see figure below) were carried out first. An appropriate precursor was synthesised for 2’-stereoselective late-stage radiofluorination based on previously developed conditions. First, the 2’-[18F]fluorinated arabino nucleoside 18F-FAU, which was considered as a rapidly accessible 2’-fluorinated uracil-based dFdC analogue was successfully synthesised in our radiochemical laboratory. Subsequently, this procedure was used as a template method to obtain the cytidine analogue 18F-FAC via a novel synthetic route in moderate radiochemical yield (4.3-5.5%, decay-corrected), high specific activity (1700 mCi/μmol) and purity (98%) after a synthesis time of 168 min.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.633561  DOI: Not available
Keywords: Q Science (General)
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