In vivo Solid Phase Microextraction for Brain Tissue Analysis

dc.contributor.authorCudjoe, Erasmus
dc.date.accessioned2014-03-31T13:37:33Z
dc.date.available2014-03-31T13:37:33Z
dc.date.issued2014-03-31
dc.date.submitted2014
dc.description.abstractNew solid phase microextraction (SPME) method was developed for brain tissue bioanalysis on a liquid chromatography mass spectrometry platform. To achieve set objectives, in vivo SPME desorption process was optimized for high throughput analysis through the development of a desorption device. Subsequently, new SPME coatings were developed for the extraction of polar neurotransmitters from biological matrices. In a targeted analysis, in vivo SPME was used to monitor of changes in the concentrations of endogenous compounds (multiple neurotransmitters) and exogenous drugs (carbamazepine and cimetidine) in the striatum of the rat brain extracellular fluid. For the first time, SPME was used for quantitative analysis of neurotransmitters and also study spacial distribution of other drugs in different regions of the brain extracellular fluid. A new approach was developed for improved metabolites coverage in a global non-targeted metabolomics studies. The proposed in vivo method showed how complementary results can be obtained through the combination of microdialysis and SPME for simultaneous sampling of the brain extracellular fluid. Finally, in a clinical application, SPME was used to monitor changes in the concentration of multiple neurotransmitters during deep brain stimulation of the pre-frontal cortex of the brain.en
dc.identifier.urihttp://hdl.handle.net/10012/8302
dc.language.isoenen
dc.pendingfalse
dc.publisherUniversity of Waterlooen
dc.subjectIn vivo solid phase microextraction for brain tissue bioanalysis with liquid chromatography mass spectrometryen
dc.subjectin vivo monitoring of endogenous and exogenous compounds in brainen
dc.subjectnew sample preparation tool for analysis of neurotransmittersen
dc.subject.programChemistryen
dc.titleIn vivo Solid Phase Microextraction for Brain Tissue Analysisen
dc.typeDoctoral Thesisen
uws-etd.degreeDoctor of Philosophyen
uws-etd.degree.departmentChemistryen
uws.peerReviewStatusUnrevieweden
uws.scholarLevelGraduateen
uws.typeOfResourceTexten

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