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The New Jersey Institute of Technology's
Electronic Theses & Dissertations Project

Title: Development of novel mass spectrometric methods for reaction screening, oligosaccharide detection, and nitrosamine quantitation
Author: Wang, Qi
View Online: njit-etd2022-085
(xviii, 154 pages ~ 6.8 MB pdf)
Department: Department of Chemistry and Environmental Science
Degree: Doctor of Philosophy
Program: Chemistry
Document Type: Dissertation
Advisory Committee: Chen, Hao (Committee chair)
Qiu, Zeyuan (Committee member)
Khalizov, Alexei (Committee member)
Zhang, Yuanwei (Committee member)
Basuray, S. (Committee member)
Date: 2022-05
Keywords: Absolute quantitation
Electrochemistry
Electrosynthesis
Mass spectrometry
Oligosaccharide detection
Availability: Unrestricted
Abstract:

Benefitting from its high detection sensitivity and specificity, mass spectrometry (MS) has become a powerful technique in academia and industry. The aim of this dissertation study is to develop new mass spectrometric methods for organic reaction screening, detection of oligosaccharide/glycan in complex matrices, and nitrosamine absolute quantitation.

First, an electrochemistry/mass spectrometry (EC/MS) platform is built to generate an N-cyclopropylaniline radical cation electrochemically and to monitor its reactivity toward alkenes, which leads to the discovery of a new redox neutral reaction of intermolecular [3 + 2] annulation of N-cyclopropylanilines and alkenes. Net redox neutral electrosynthesis is quite rare in synthetic organic electrochemistry. Taking full advantage of the online EC/MS platform as a screening tool which only uses 50 nmol of substrates, a large scale electrosynthesis for 4-chloro-N-(2-phenylcyclopentyl)aniline in 128 mg is successfully conducted in an electrochemical cell. Such an EC/MS screening of reaction may expedite the discovery of other novel redox neutral electrochemical reactions.

Second, conventional MS-based analytical methods for carbohydrates are time-consuming because of offline sample pretreatment to remove matrix which suppresses MS signal. A fast and sensitive MS-based oligosaccharide characterization strategy is developed, termed desalting paper spray mass spectrometry (DPS-MS), that uses a piece of triangular paper (10 mm x 5 mm, height x base) for both carbohydrate desalting and subsequent ionization for analysis of various oligosaccharide types of analytes in complex nonvolatile buffers (Tris-HC1, PBS, and HEPES), and glycosyltransferases (GT) reaction products. This new analytical method is not only fast (<5 min per sample) and straightforward but is also highly sensitive (LOD of 1.1 nM for β-cyclodextrin). Furthermore, DPS-MS quantitative analysis of acceptor sugars in GT reactions control samples afford a slight deviation (6.5%-11.6%) from theoretical values. This vital result shows excellent potential for onsite, high-throughput characterization of GT activities and carbohydrate diagnostics by DPS-MS.

Third, N-Nitrosamines, possible carcinogenic substrates, are recently found in the sartan family of drugs and led to drug recalls. Their detection and quantification are therefore of significant importance for human health. Although many literature quantitation papers reported, they focused on simple nitrosamines, relying on the use of standards. Nevertheless, quantitation of nitrosamines directly derived from drug molecules with a complicated structure is not explored, due to the grand challenge of lacking standards that are difficult and expensive to synthesize. A novel absolute quantitation approach for N-nitrosamines using coulometric mass spectrometry (CMS) based on Faraday's Law is explored. In this approach, reductive conversion of N-nitrosamines into electrochemically active hydrazines is accomplished using zinc as a reductant under acidic conditions and hydrazines are then easily quantified using CMS, without using standards.


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