University of Louisville - Chemistry
Biochemistry and Genetics Course Representative
Sara worked at University of Louisville School of Medicine as a Biochemistry and Genetics Course Representative
Tutor
Sara worked at University of Louisville School of Medicine as a Tutor
Graduate Teaching Assistant
Give pre-lab lecture to prepare students for upcoming lab, assist students while performing lab if necessary, grade quizzes and lab reports weekly, grade final at end of semester
Biochemistry Course Representative
Sara worked at University of Louisville as a Biochemistry Course Representative
Senior Instructor
Oversee undergraduate and graduate teaching assistants for organic labs (Chem 343 and Chem 344)
Resident Assistant
Sara worked at University of Louisville Housing as a Resident Assistant
Doctor of Medicine - MD
Biochemistry and Genetics Course Representative
Tutor
Master of Science (M.S.)
Chemistry
Doctor of Philosophy (PhD)
Chemistry
Dissertation: Magnetic Field-Induced Intramolecular Cyclization as a Trigger for Nanoparticle-Based Delivery Systems
Graduate Teaching Assistant
Give pre-lab lecture to prepare students for upcoming lab, assist students while performing lab if necessary, grade quizzes and lab reports weekly, grade final at end of semester
Biochemistry Course Representative
Senior Instructor
Oversee undergraduate and graduate teaching assistants for organic labs (Chem 343 and Chem 344)
Analytical Methods
Synthesis and application of isotopically labeled N-methoxy-N-(2-aminooxyethyl)-propionate (MAP), a chemoselective carbonyl derivatization reagent, is reported. To exploit the ready measurement of fragments serving as reporter ions in the m/z 32–34 range, MAP is designed to undergo electron ionization (EI)-induced fragmentation to expel labeled ethyl carbenium ions for relative quantifications in multiplexed analyses. A study of the EI-MS fragmentation behavior of a panel of MAP–carbonyl adducts revealed that the N-methoxy amide motif of MAP is highly predisposed to undergo carbonyl alpha cleavage to produce corresponding labeled carbenium ions in the targeted m/z range. Use of the N-methoxy amide functionality decreased undesired (e.g., uninformative) mass spectral fragmentations as well as provided good resistance to cleavage by amines or base relative to ester functionality. These properties should facilitate the use of MAP in multiplexed GC-MS analyses of complex mixtures containing aldehyde and ketone analytes. A representative multiplexed experiment using MAP isotopologues illustrates this approach for quantification of a carbonyl analyte in pooled sample mixtures.