A. Ceccato et al., Enantiomeric separation of pirlindole by liquid chromatography using different types of chiral stationary phases, J PHARM B, 18(4-5), 1998, pp. 605-614
The enantioseparation of pirlindole by liquid chromatography (LC) was inves
tigated using three different chiral stationary phases (CSPs) containing ei
ther cellulose tris-(3,5-dimethylphenylcarbamate) (Chiralcel OD-R), ovomuco
id (OVM) or beta-cyclodextrin (beta-CD). The effects of the: mobile phase p
H on retention, enantioselectivity and resolution were studied. Methanol an
d acetonitrile were tested, as organic modifiers while the influence of the
addition to the mobile phase of sodium alkanesulfonates or sodium perchlor
ate was also investigated. Sodium perchlorate was only used on the Chiralce
l OD-R column while sodium alkanesulfonates were tested as mobile phase add
itives on the three kinds of CSPs. The enantioseparation of pirlindole coul
d be obtained on all CSPs tested, the best results with respect to chiral r
esolution being achieved on the Chiralcel QD-R and the OVM columns. The use
of sodium octanesulfonate (NaOS) was found to improve the enantioseparatio
n of pirlindole on the OVM column while enantioselectivity was considerably
enhanced by addition of sodium perchlorate on the Chiralcel OD-R column. (
C) 1997 Elsevier Science B.V. All rights reserved.