Literature DB >> 16275290

Rational method development strategies on a fluorinated liquid chromatography stationary phase: mobile phase ion concentration and temperature effects on the separation of ephedrine alkaloids.

David S Bell1, Hugh M Cramer, A Daniel Jones.   

Abstract

Fluorinated, silica-based stationary phases are becoming increasingly popular alternatives to traditional alkyl phases owing to their differential selectivity and retention for a variety of analyte classes. In this report, the ion-exchange mechanisms characteristic of a fluorinated phase are exploited to rapidly develop separation conditions for ephedrine alkaloids and synephrine using a mobile phase compatible with mass spectrometry. A linear relationship of basic analyte retention with the reciprocal of ammonium acetate concentration is first established. This linear relationship can then be used to optimize retention and selectivity in just two experiments. The relationship of retention with temperature is also explored. Greater retention with increasing temperature is demonstrated on the fluorinated phase at high percentages of organic modifier, which is in contrast to behavior observed in typical reversed-phase separations. The unexpected observation is explicated based on the reduction in solvent solvating power with increasing temperature. As solvation power of the mobile phase decreases, decreased solvation of both mobile phase and ionized surface groups of the stationary phase leads to stronger interactions between analyte and stationary phase. Both mobile phase ion concentration and temperature are shown to be powerful tools for the manipulation of analyte retention and selectivity.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16275290     DOI: 10.1016/j.chroma.2005.08.004

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  5 in total

1.  Simultaneous quantification of intracellular natural and antiretroviral nucleosides and nucleotides by liquid chromatography-tandem mass spectrometry.

Authors:  Emilie Fromentin; Christina Gavegnano; Aleksandr Obikhod; Raymond F Schinazi
Journal:  Anal Chem       Date:  2010-03-01       Impact factor: 6.986

2.  Streamlined pentafluorophenylpropyl column liquid chromatography-tandem quadrupole mass spectrometry and global (13)C-labeled internal standards improve performance for quantitative metabolomics in bacteria.

Authors:  Song Yang; Martin Sadilek; Mary E Lidstrom
Journal:  J Chromatogr A       Date:  2010-09-29       Impact factor: 4.759

3.  One-pot discriminant LC/MS quantitative analysis of ephedrine and pseudoephedrine using Finger Masher and their distribution in the aerial stems of Ephedra plants.

Authors:  Hiroyuki Fuchino; Osamu Iida; Noriaki Kawano; Nobuo Kawahara; Kayo Yoshimatsu
Journal:  J Nat Med       Date:  2021-02-18       Impact factor: 2.343

Review 4.  Alkaloids of the Genus Datura: Review of a Rich Resource for Natural Product Discovery.

Authors:  Maris A Cinelli; A Daniel Jones
Journal:  Molecules       Date:  2021-04-30       Impact factor: 4.411

5.  Origin of the selectivity differences of aromatic alcohols and amines of different n-alkyl chain length separated with perfluorinated C8 and bidentated C8 modified silica hydride stationary phases.

Authors:  Chadin Kulsing; Yada Nolvachai; Maria T Matyska; Joseph J Pesek; Joshua Topete; Reinhard I Boysen; Milton T W Hearn
Journal:  Anal Chim Acta X       Date:  2018-12-28
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.