4.7 Article

Multi-modal applicability of a reversed-phase/weak-anion exchange material in reversed-phase, anion-exchange, ion-exclusion, hydrophilic interaction and hydrophobic interaction chromatography modes

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 400, 期 8, 页码 2517-2530

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-011-4755-3

关键词

Mixed-mode stationary phase; Reversed-phase/weak anion-exchange material; Hydrophilic interaction chromatography (HILIC); Hydrophobic interaction chromatography (HIC); Ion-exclusion chromatography

资金

  1. Christian-Doppler Research Society
  2. piCHEM (Graz, Austria)
  3. Merck KGaA (Darmstadt, Germany)
  4. Sandoz (Kundl, Austria)
  5. Fresenius Kabi Austria (Graz, Austria)
  6. AstraZeneca (Molndal, Sweden)

向作者/读者索取更多资源

We recently introduced a mixed-mode reversed-phase/weak anion-exchange type separation material based on silica particles which consisted of a hydrophobic alkyl strand with polar embedded groups (thioether and amide functionalities) and a terminal weak anion-exchange-type quinuclidine moiety. This stationary phase was designed to separate molecules by lipophilicity and charge differences and was mainly devised for peptide separations with hydroorganic reversed-phase type elution conditions. Herein, we demonstrate the extraordinary flexibility of this RP/WAX phase, in particular for peptide separations, by illustrating its applicability in various chromatographic modes. The column packed with this material can, depending on the solute character and employed elution conditions, exploit attractive or repulsive electrostatic interactions, and/or hydrophobic or hydrophilic interactions as retention and selectivity increments. As a consequence, the column can be operated in a reversed-phase mode (neutral compounds), anion-exchange mode (acidic compounds), ion-exclusion chromatography mode (cationic solutes), hydrophilic interaction chromatography mode (polar compounds), and hydrophobic interaction chromatography mode (e.g., hydrophobic peptides). Mixed-modes of these chromatographic retention principles may be materialized as well. This allows an exceptionally flexible adjustment of retention and selectivity by tuning experimental conditions. The distinct separation mechanisms will be outlined by selected examples of peptide separations in the different modes.

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