The Applicability of Chromatographic Retention Modeling on Chiral Stationary Phases in Reverse-Phase Mode: A Case Study for Ezetimibe and Its Impurities.

AQbD DryLab chiral stationary phase experimental design ezetimibe mechanistic model related substances retention modeling

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
08 Nov 2023
Historique:
received: 16 09 2023
revised: 01 11 2023
accepted: 06 11 2023
medline: 27 11 2023
pubmed: 25 11 2023
entrez: 25 11 2023
Statut: epublish

Résumé

Mechanistic modeling is useful for predicting and modulating selectivity even in early chromatographic method development. This approach is also in accordance with current analytical quality using design principles and is highly welcomed by the authorities. The aim of this study was to investigate the separation behavior of two different types of chiral stationary phases (CSPs) for the separation of ezetimibe and its related substances using the mechanistic retention modeling approach offered by the Drylab software (version 4.5) package. Based on the obtained results, both CSPs presented with chemoselectivity towards the impurities of ezetimibe. The cyclodextrin-based CSP displayed a higher separation capacity and was able to separate seven related substances from the active pharmaceutical ingredient, while the cellulose-based column enabled the baseline resolution of six impurities from ezetimibe. Generally, the accuracy of predicted retention times was lower for the polysaccharide CSP, which could indicate the presence of additional secondary interactions between the analytes and the CSP. It was also demonstrated that the combination of mechanistic modeling and an experimental design approach can be applied to method development on CSPs in reverse-phase mode. The applicability of the methods was tested on spiked artificial placebo samples, while intraday and long-term (2 years) method repeatability was also challenged through comparing the obtained retention times and resolution values. The results indicated the excellent robustness of the selected setpoints. Overall, our findings indicate that the chiral columns could offer orthogonal selectivity to traditional reverse-phase columns for the separation of structurally similar compounds.

Identifiants

pubmed: 38003286
pii: ijms242216097
doi: 10.3390/ijms242216097
pmc: PMC10671152
pii:
doi:

Substances chimiques

Ezetimibe EOR26LQQ24
Polysaccharides 0
Cellulose 9004-34-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Elek Ferencz (E)

Department of Physical Chemistry, Faculty of Pharmacy, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.
Gedeon Richter Romania S.A., Analytical Development Department, 540306 Targu Mures, Romania.

Éva-Katalin Kelemen (ÉK)

Gedeon Richter Romania S.A., Analytical Development Department, 540306 Targu Mures, Romania.

Mona Obreja (M)

Gedeon Richter Romania S.A., Analytical Development Department, 540306 Targu Mures, Romania.

Gergő Tóth (G)

Department of Pharmaceutical Chemistry, Semmelweis University, 1083 Budapest, Hungary.

Melinda Urkon (M)

Department of Pharmacology and Clinical Pharmacy, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.

Arnold Zöldhegyi (A)

Molnár-Institute for Applied Chromatography, 10407 Berlin, Germany.

Emese Sipos (E)

Department of Pharmaceutical Industry and Management, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.

Zoltán-István Szabó (ZI)

Department of Pharmaceutical Industry and Management, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.
Sz-imfidum Ltd., 525401 Lunga, Romania.

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