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Implementation of a design space approach for enantiomeric separations in polar organic solvent chromatography

Authors :
Eduard Badarau
Attilio Ceccato
Pierre Lebrun
Radu Oprean
Fabien Dufour
Frédéric Lecomte
Ines Slama
Iolanda Nistor
Philippe Hubert
Eric Rozet
Katina Sourou Sylvestre Dossou
Jean-François Liégeois
Marianne Fillet
Source :
Journal of Pharmaceutical and Biomedical Analysis. 74:273-283
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

This paper focuses on implementing a design space approach and on the critical process parameters (CPPs) to consider when applying the Quality by Design (QbD) concepts outlined in ICH Q8(R2), Q9 and Q10 to analytical method development and optimization for three chiral compounds developed as modulators of small conductance calcium-activated potassium (SK) channels. In this sense, an HPLC method using a polysaccharide-based stationary phase containing a cellulose tris (4-chloro-3-methylphenylcarbamate) chiral selector in polar organic solvent chromatography mode was considered. The effects of trifluoroacetic acid (TFA) and n-hexane concentration in an acetonitrile (MeCN) mobile phase were investigated under a wide range of column temperatures. Good correlations were found between the observed data obtained after using a central composite design and the expected chromatographic behaviours predicted by applying the design of experiments-design space (DoE-DS) methodology. The critical quality attribute represented here by the separation criterion (Scrit) allowed assessing the quality of the enantioseparation. Baseline separation for the compounds of interest in an analysis time of less than 20 min was possible due to the original and powerful tools applied which facilitated an enhanced method comprehension. Finally, the advantage of the DoE-DS approach resides in granting the possibility to concurrently assess robustness and identify the optimal conditions which are compound dependent.

Details

ISSN :
07317085
Volume :
74
Database :
OpenAIRE
Journal :
Journal of Pharmaceutical and Biomedical Analysis
Accession number :
edsair.doi.dedup.....1cd5f1202ebfa452691e586bc7f24586
Full Text :
https://doi.org/10.1016/j.jpba.2012.10.015