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Journal ArticleDOI

Practical implications of some recent studies in electrospray ionization fundamentals.

TLDR
Fundamental studies of the ESI process are reviewed that are relevant to issues related to analyte chargeability and surface activity, and how accessible parameters such as nonpolar surface area and reversed phase HPLC retention time can be used to predict relative ESI response.
Abstract
In accomplishing successful electrospray ionization analyses, it is imperative to have an understanding of the effects of variables such as analyte structure, instrumental parameters, and solution composition. Here, we review some fundamental studies of the ESI process that are relevant to these issues. We discuss how analyte chargeability and surface activity are related to ESI response, and how accessible parameters such as nonpolar surface area and reversed phase HPLC retention time can be used to predict relative ESI response. Also presented is a description of how derivitizing agents can be used to maximize or enable ESI response by improving the chargeability or hydrophobicity of ESI analytes. Limiting factors in the ESI calibration curve are discussed. At high concentrations, these factors include droplet surface area and excess charge concentration, whereas at low concentrations ion transmission becomes an issue, and chemical interference can also be limiting. Stable and reproducible non-pneumatic ESI operation depends on the ability to balance a number of parameters, including applied voltage and solution surface tension, flow rate, and conductivity. We discuss how changing these parameters can shift the mode of ESI operation from stable to unstable, and how current-voltage curves can be used to characterize the mode of ESI operation. Finally, the characteristics of the ideal ESI solvent, including surface tension and conductivity requirements, are discussed. Analysis in the positive ion mode can be accomplished with acidified methanol/water solutions, but negative ion mode analysis necessitates special constituents that suppress corona discharge and facilitate the production of stable negative ions.

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Journal ArticleDOI

Imaging mass spectrometry

TL;DR: Many of the instrumental developments and methodological approaches responsible for an increasing upsurge in interest in imaging mass spectrometry are reviewed, compare and contrast the information provided by SIMS and MALDI imaging, and discuss future possibilities.
Journal ArticleDOI

Electrospray: From ions in solution to ions in the gas phase, what we know now

TL;DR: The following processes are considered: Creation of charge droplets at the capillary tip; Electrical potentials required and possibility of gas discharges; Evolution of charged droplets, due to solvent evaporation and Coulomb explosions, to very small droplets that are the precursors of the gas phase ions.
Journal ArticleDOI

An overview of matrix effects in liquid chromatography-mass spectrometry.

TL;DR: This review gives a detailed description on when matrix effects (ME) might be expected, and how they can be evaluated, and the main strategies to overcome these phenomena are described in detail.
Journal ArticleDOI

Chemical derivatization and mass spectral libraries in metabolic profiling by GC/MS and LC/MS/MS

TL;DR: The potential of derivatization for metabolic profiling in LC/MS is demonstrated by the enhanced analysis of plant extracts, including the potential to measure volatile acids such as formic acid, difficult to achieve by GC/MS.
Journal ArticleDOI

Mass spectrometry in metabolome analysis

TL;DR: This review is mainly focused on the status of MS in the metabolome field, trying to direct the reader to the main approaches for analysis of metabolites, reviewing basic methodologies in sample preparation, and the most recent MS techniques introduced.
References
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Journal ArticleDOI

Electrospray ionization for mass spectrometry of large biomolecules

TL;DR: Spectra have been obtained for biopolymers including oligonucleotides and proteins, the latter having molecular weights up to 130,000, with as yet no evidence of an upper limit.
Journal ArticleDOI

Analytical properties of the nanoelectrospray ion source.

TL;DR: Improved desolvation in nanoES led to instrument-limited resolution of the signals of a glycoprotein and the ability to signal average extensively allowed the C-terminal sequencing of a 40 kDa protein.
Journal ArticleDOI

Molecular Beams of Macroions

TL;DR: In this article, the authors demonstrate that definite mass/charge states can be formed by electrospraying a dilute polymer solution into an evaporation chamber, negative macroions can be produced and a molecular beam formed by sampling the gaseous mixture of macroions, solvent and nitrogen molecules with a nozzle-skimmer system of the Kantrowitz-Gray type.
Journal ArticleDOI

On the evaporation of small ions from charged droplets

TL;DR: In this paper, a theoretical argument is developed to find in which conditions this ion evaporation can occur; to that end solvation free enthalpies of cluster ions are derived from existing experimental data and the absolute reaction rate theory is applied.
Journal ArticleDOI

The effects of sample preparation methods on the variability of the electrospray ionization response for model drug compounds.

TL;DR: A post-column infusion system was developed in order to analyze suppression of electrospray ionization (ESI) tandem mass spectrometry response in the presence of endogenous plasma interferences and demonstrated that ESI response suppression is compound dependent.
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