Date of Submission

5-2024

Document Type

Thesis

Degree Name

Master of Science in Chemistry

Department

Chemistry and Chemical Engineering

Advisor

Robert Powers, Ph.D.

Keywords

Methamphetamine, Amphetamine, Methylation by Phenylethanolamine n-Methyltransferase (PNMT), Human Cytosol Mix

MeSH

Methamphetamine, Amphetamine, Methylation, Methyltransferases, Cytosol

LCSH

Methamphetamine, Amphetamine abuse, Methylation, Methyltransferases, Cytosol

Abstract

In current forensic analysis, the presence of methamphetamine in a sample is routinely presumed to reflect methamphetamine abuse. This is due to the expectation that individuals either abusing, or receiving amphetamine for therapeutic purposes (e.g. as treatment for ADHD) will not generate any significant levels of methamphetamine as a product of metabolism. We have hypothesized however, that because amphetamine can serve as a substrate for methylation by phenylethanolamine n-methyltransferase (PNMT), (which will be in equilibrium with the reverse demethylation reaction) some individuals chronically taking amphetamine for therapeutic purposes may generate low levels of methamphetamine that would show up on a drug test. We expect that the equilibrium between amphetamine and methamphetamine is determined by both the steady-state concentration of amphetamine and product inhibition of PNMT by methamphetamine. A method for the evaluation of methylation of amphetamine in human cytosol mix has already been developed. This study aims to continue previous work through adapting previous methodology for a pure PNMT assay, and developing a methodology for sample analysis with the Schimadzu GCMS-QP2010 SE Single Quadrupole GC-MS.

Included in

Chemistry Commons

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