Evidence map›Paper›PMID 42796543›Full record

ReviewMolecules (Basel, Switzerland)2026

Capillary Electrophoretic Enantioseparation of Profens: Advances in Chiral Selectors, Separation Strategies, and Analytical Applications.

Gabriel Hancu, Maria Matean, Anca Gabriela Cârje

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Gabriel HancuDepartment of Pharmaceutical and Therapeutic Chemistry, Faculty of Pharmacy, "George Emil Palade" University of Medicine, Pharmacy, Science and Technology of Târgu Mures, 540120 Târgu Mures, Romania.ORCID 0000-0003-2564-9271
Maria MateanDepartment of Analytical Chemistry and Drug Analysis, Faculty of Pharmacy, "George Emil Palade" University of Medicine, Pharmacy, Science and Technology of Târgu Mures, 540120 Târgu Mures, Romania.
Anca Gabriela CârjeDepartment of Analytical Chemistry and Drug Analysis, Faculty of Pharmacy, "George Emil Palade" University of Medicine, Pharmacy, Science and Technology of Târgu Mures, 540120 Târgu Mures, Romania.ORCID 0000-0001-8044-3036

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Profens are chiral nonsteroidal anti-inflammatory drugs (NSAIDs) whose enantiomers may differ in pharmacokinetics, pharmacological activity and pharmacotoxicological profile, making enantioselective analysis relevant for pharmaceutical quality control and bioanalytical applications. Capillary electrophoresis (CE) has been extensively investigated for their enantioseparation because of its high efficiency, low sample and reagent consumption, and the possibility of easily modifying the chiral recognition environment. This review traces the development of CE methods for profen enantioseparation from early exploratory studies focused on chiral selector (CS) screening to the most recent reports available up to 2026, highlighting the progressive shift toward quantitative, validated, and application-oriented methods. The influence of CS type and concentration, background electrolyte (BGE) composition and pH, organic modifiers, polarity, and capillary surface modification is discussed in relation to enantioselectivity and analytical performance. Although cyclodextrin (CD)-based systems remain predominant, the available literature shows that profen enantioseparation is strongly analyte-dependent and that no single CS or set of conditions is universally applicable. The review also examines the transition from proof-of-concept enantioseparation toward validated methods for enantiomeric impurity determination, configurational stability assessment, and the analysis of pharmaceutical, biological, and environmental samples, while highlighting the analytical performance and current limitations of CE-based approaches. Future developments should focus on improving sensitivity, robustness, and applicability to complex matrices while making greater use of rational CS selection, multivariate optimization, and complementary detection approaches.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalCyclodextrinsElectrophoresis, CapillaryHumansHydrogen-Ion ConcentrationStereoisomerismAnti-Inflammatory Agents, Non-SteroidalCyclodextrinscapillary electrophoresischiralitychiral selectorscyclodextrinsenantiomeric purityenantioseparationNSAIDsprofens

Identifiers

PMID42796543
PMCPMC13609797

What OpenQuestion holds

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Registered trials

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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.