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Updated: Aug 24, 2025

Online Size-exclusion and Ion-exchange Chromatography on a SAXS Beamline
Published on: January 5, 2017
Sense and nonsense of shifting gradients in on-line comprehensive reversed-phase LC × reversed-phase LC
Soraya Chapel1, Florent Rouvière1, Sabine Heinisch1
1Université de Lyon, Institut des Sciences Analytiques, UMR 5280, CNRS, ENS Lyon, 5 rue de la Doua, 69100 Villeurbanne, France.
Abstract:
In on-line comprehensive two-dimensional liquid chromatography (LC × LC), the combination of similar chromatographic modes such as reversed-phase liquid chromatography × reversed-phase liquid chromatography (RPLC × RPLC) usually leads to the partial occupation of the available separation space. A possible solution to circumvent this issue may be to dynamically adjust the gradient elution in the second dimension (2D) throughout the LC × LC analysis. This allows the gradient elution to be tailored to the elution conditions of each fraction instead of using a conventional full gradient program in which the same gradient profile is repeated for each 2D-fraction. In this study, an online RPLC × RPLC method is optimized with shifting gradients in 2D. The logic behind implementing such programs in on-line LC × LC is explained. The optimized method consists of a combination of segmented and shifted gradient modes. It is shown that the retention space coverage can be increased by 50 % compared to a conventional full gradient program, leading to a significant increase in peak capacity (about 35 %). However, such an increase comes at the expense of larger peak widths in 2D and thus lower peak intensities. It is shown here that the use of shifting gradients raises another serious issue related to the repeatability of retention times between two successive 2D-separations.
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