Sense and nonsense of shifting gradients in on-line comprehensive reversed-phase LC × reversed-phase LC.

J Chromatogr B Analyt Technol Biomed Life Sci

Université de Lyon, Institut des Sciences Analytiques, UMR 5280, CNRS, ENS Lyon, 5 rue de la Doua, 69100 Villeurbanne, France.

Published: December 2022

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 (D) 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 D-fraction. In this study, an online RPLC × RPLC method is optimized with shifting gradients in D. 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 D 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 D-separations.

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Source
http://dx.doi.org/10.1016/j.jchromb.2022.123512DOI Listing

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