Issue 20, 2015

Using differential mobility spectrometry to measure ion solvation: an examination of the roles of solvents and ionic structures in separating quinoline-based drugs

Abstract

Understanding the mechanisms and energetics of ion solvation is critical in many scientific areas. Here, we present a methodlogy for studying ion solvation using differential mobility spectrometry (DMS) coupled to mass spectrometry. While in the DMS cell, ions experience electric fields established by a high frequency asymmetric waveform in the presence of a desired pressure of water vapor. By observing how a specific ion's behavior changes between the high- and low-field parts of the waveform, we gain knowledge about the aqueous microsolvation of that ion. In this study, we applied DMS to investigate the aqueous microsolvation of protonated quinoline-based drug candidates. Owing to their low binding energies with water, the clustering propensity of 8-substituted quinolinium ions was less than that of the 6- or 7-substituted analogues. We attribute these differences to the steric hinderance presented by subtituents in the 8-position. In addition, these experimental DMS results were complemented by extensive computational studies that determined cluster structures and relative thermodynamic stabilities.

Graphical abstract: Using differential mobility spectrometry to measure ion solvation: an examination of the roles of solvents and ionic structures in separating quinoline-based drugs

Supplementary files

Article information

Article type
Paper
Submitted
28 apr 2015
Accepted
03 iyl 2015
First published
03 iyl 2015

Analyst, 2015,140, 6897-6903

Author version available

Using differential mobility spectrometry to measure ion solvation: an examination of the roles of solvents and ionic structures in separating quinoline-based drugs

C. Liu, J. C. Y. Le Blanc, J. Shields, J. S. Janiszewski, C. Ieritano, G. F. Ye, G. F. Hawes, W. S. Hopkins and J. L. Campbell, Analyst, 2015, 140, 6897 DOI: 10.1039/C5AN00842E

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