Abstract
Rapid optimization of gradient liquid chromatographic (LC) separations often utilizes analyte retention modelling to predict retention times as function of eluent composition. However, due to the dwell volume and technical imperfections, the actual gradient may deviate from the set gradient in a fashion unique to the employed instrument. This makes accurate retention modelling for gradient LC challenging, in particular when very fast separations are pursued. Although gradient deformation has been addressed in method-transfer situations, it is rarely taken into account when reporting analyte retention parameters obtained from gradient LC data, hampering the comparison of data from various sources. In this study, a response-function-based algorithm was developed to determine analyte retention parameters corrected for geometry-induced deformations by specific LC instruments. Out of a number of mathematical distributions investigated as response-functions, the so-called “stable function” was found to describe the formed gradient most accurately. The four parameters describing the model resemble the statistical moments of the distribution and are related to chromatographic parameters, such as dwell volume and flow rate. The instrument-specific response function can then be used to predict the actual shape of any other gradient programmed on that instrument. To incorporate the predicted gradient in the retention modelling of the analytes, the model was extended to facilitate an unlimited number of linear gradient steps to solve the equations numerically. The significance and impact of distinct gradient deformation for fast gradients was demonstrated using three different LC instruments. As a proof of principle, the algorithm and retention parameters obtained on a specific instrument were used to predict the retention times on different instruments. The relative error in the predicted retention times went down from an average of 9.8% and 12.2% on the two other instruments when using only a dwell-volume correction to 2.1% and 6.5%, respectively, when using the proposed algorithm. The corrected retention parameters are less dependent on geometry-induced instrument effects.
Original language | English |
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Article number | 461714 |
Pages (from-to) | 1-9 |
Number of pages | 9 |
Journal | Journal of Chromatography A |
Volume | 1635 |
Early online date | 13 Nov 2020 |
DOIs | |
Publication status | Published - 4 Jan 2021 |
Funding
TB, LN, SM, PS, GS and BP acknowledge the UNMATCHED project, which is supported by BASF, DSM and Nouryon, and receives funding from the Dutch Research Council (NWO) in the framework of the Innovation Fund for Chemistry and from the Ministry of Economic Affairs in the framework of the “PPS-toeslagregeling”. BP acknowledges the Agilent UR grant #4354. MU acknowledge the TooCOLD project, which is part of the TTW Open Technology Programma with project number 15506 which is (partly) financed by the Dutch Research Council (NWO).
Funders | Funder number |
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Agilent UR | 4354, 15506 |
BASF | |
Ministerie van Economische Zaken | |
Nederlandse Organisatie voor Wetenschappelijk Onderzoek | |
China Academy of Space Technology | |
DSM Research |
Keywords
- gradient deformation
- multi-step gradients
- optimization
- response functions
- retention modelling