The use of a circular dichroism (CD) based HPLC detection system was recent
ly described by some authors and proposed for a nonenantioselective HPLC en
antiomeric purity determination. Indeed the system, measuring both CD and U
V signals simultaneously, allows the evaluation of the g anisotropy factor.
In order to experimentally support such an analytical procedure as an alte
rnative to the enantioselective chromatographic method currently found in s
ome pharmacopocial monographs, we have studied its application to the analy
sis of dexchlorpheniramine maleate, an active substance which exhibits a po
or CD signal in the 250-270 nm spectral region with a g value of the order
of 10(-4). The results reported indicate that the suitability of the studie
d procedure for the enantiomeric purity determination is obtained only when
the CD-detector reaches high stability, indeed a certain time lag is syste
matically necessary to obtain stable responses, i.e. adequate precision. Th
e enantioselective HPLC procedure seems to be more precise for enantiomeric
purity values less than or equal to2% than the CD based detection system;
such a disadvantage might be counterbalanced by the use of non chiral stati
onary phases. (C) 2001 Elsevier Science B.V. All rights reserved.