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Updating a chiral separation strategy for non-acidic drugs with capillary electrochromatography applicable for both chlorinated and non-chlorinated polysaccharide selectors

✍ Scribed by Ans Hendrickx; Debby Mangelings; Bezhan Chankvetadze; Yvan Vander Heyden


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
265 KB
Volume
32
Category
Article
ISSN
0173-0835

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✦ Synopsis


Abstract

A generic strategy for the chiral separation of non‐acidic pharmaceuticals was updated to complete an approach defined earlier. The selected chiral stationary phases are all polysaccharide selectors, chlorinated, and non‐chlorinated, namely Lux^®^ Amylose 2, Chiralcel^®^ OD‐RH, Lux^®^ Cellulose 4, and Chiralpak^®^ AD‐RH. In this study, the screening step of a strategy defined earlier was updated and the optimization steps were re‐evaluated for the applied chiral stationary phases. These screening and optimization conditions were studied by analyzing 20 pharmaceuticals at different organic modifier contents, temperatures, or applied voltages. The proposed chiral separation strategy was then evaluated with a test set of 19 non‐acidic drugs. Seventeen compounds (89.5%) of the latter set could be resolved of which eight (42%) were baseline separated. The strategy thus proved to be applicable on compounds different from those used for its development.