Evidence map›Paper›PMID 42159681›Full record

ArticleAnalytical and bioanalytical chemistry2026

Enantioseparation of proton pump inhibitors using multimodal chiral cation exchangers.

Magdaléna Labíková, Adam Pospíšil, Ondřej Znamínko, Wolfgang Lindner, Elisa Bianconi, Gina Cavaliere, Roccaldo Sardella, Andrea Carotti, Michal Kohout

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Article in Analytical and bioanalytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Magdaléna LabíkováDepartment of Organic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28, Prague, Czech Republic.
Adam PospíšilDepartment of Organic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28, Prague, Czech Republic.
Ondřej ZnamínkoDepartment of Organic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28, Prague, Czech Republic.
Wolfgang LindnerInstitute of Analytical Chemistry, University of Vienna, Währingerstrasse 38, 1090, Vienna, Austria.
Elisa BianconiDepartment of Pharmaceutical Sciences, University of Perugia, Via Palazzeschi N. 9, 06126, Perugia, Italy.
Gina CavaliereDepartment of Pharmaceutical Sciences, University of Perugia, Via Palazzeschi N. 9, 06126, Perugia, Italy.
Roccaldo SardellaDepartment of Pharmaceutical Sciences, University of Perugia, Via Palazzeschi N. 9, 06126, Perugia, Italy.
Andrea CarottiDepartment of Pharmaceutical Sciences, University of Perugia, Via Palazzeschi N. 9, 06126, Perugia, Italy. andrea.carotti@unipg.it.
Michal KohoutDepartment of Organic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28, Prague, Czech Republic. michal.kohout@vscht.cz.

Funding

NextGenerationEU Grant ECS00000041 - VITALITY - CUP J97G220001700
6 · The paper itself

Abstract

The growing demand for enantioselective pharmaceutical analysis has prompted the development of novel chiral stationary phases (CSPs) tailored for high-performance liquid chromatography (HPLC). More recently, particular attention has been paid to multimodal (mixed-mode) stationary phases, which combine several interaction principles and broaden the applicability of the CSP. In this study, multimodal CSPs based on N-(3,5-dinitrobenzoyl)-tyrosine derivatives, featuring both donor-acceptor and ion-exchange/ion-pairing functionalities, were applied for the enantioseparation of omeprazole, pantoprazole, and lansoprazole, widely used proton pump inhibitors. Two in-house-developed CSPs were evaluated under multiple chromatographic modes, using polar-organic (PO), polar-organic-water (POW), and normal-phase (NP) mobile-phase conditions. PO and POW modes were selected as optimal due to their MS compatibility and sustainable solvent composition. The effect of mobile-phase composition, including MeCN/MeOH ratio and acidic/basic additives, on retention and enantioselectivity was systematically studied. The optimized method enabled the direct analysis of omeprazole enantiomers in a commercial tablet formulation using LC-MS. In parallel, molecular dynamics (MD) simulations were employed to investigate the mechanistic basis of chiral recognition at the molecular level. Key interaction energies and conformational behaviors were analyzed, supporting the experimentally observed enantioselectivity trends and providing insight into the spatial arrangement of the chiral selector-analyte associates. These findings highlight the potential of tyrosine-based multimodal CSPs for robust enantioselective analysis of PPI-type drugs under UV and MS-compatible conditions.

Indexed as

Chiral cation exchangersEnantiorecognitionEnantioseparationMolecular dynamicsPump inhibitors

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.