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  • The effect of achiral calixarenes on chiral separation of propranolol-HCl and brompheniramine maleate in capillary electrophoresis using cyclodextrin as chiral selector.

The effect of achiral calixarenes on chiral separation of propranolol-HCl and brompheniramine maleate in capillary electrophoresis using cyclodextrin as chiral selector.

Die Pharmazie (2008-05-13)
H Hashem, M Kinzig, T Jira
RESUMEN

In this study we have examined the effect of achiral water soluble p-sulfonatocalixarenes (SCX[n]) on chiral separation propranolol-HCl and brompheniramine maleate. Several cyclodextrins (CDs) and cyclodextrin derivatives were examined as chiral selectors applying complete filling technique (CFT) accompanied with the partial filling technique PFT of (SCX[n]) as achiral modifier. Only with hydroxypropyl-beta-cyclodextrin (HP-beta-CD) chiral separation could be achieved. The effect of the organic modifier on these chiral separations was examined. The results indicate that at pH 4.65, the use of HP-beta-CD (CFT) alone could not initiate chiral separations of both analytes and these chiral separations could be induced using HP-beta-CD (CFT) followed by SCX[n]/HP-beta-CD (PFT).

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Supelco
Brompheniramine maleate solution, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®