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Electrophoresis ; 26(20): 3930-41, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16167306

ABSTRACT

In completion of an earlier defined generic chiral screening approach, a generic separation strategy for basic, bifunctional, and neutral compounds was proposed and evaluated. This strategy adds to a previously defined strategy for acidic compounds. The screening experiment of the actual strategy used a mobile phase of 5 mM phosphate buffer pH 11.5/ACN (30/70 v/v), a temperature of 25 degrees C, and a voltage of 15 kV. The selected chiral stationary phases were Chiralpak AD-RH, Chiralcel OD-RH, Chiralcel OJ-RH, and Chiralpak AS-RH, all based on polysaccharide selectors. It was seen that 31 out of 48 test compounds were partially or baseline-resolved under screening conditions. After execution of the optimization steps of the strategy, this number increased to 41, with a total of 21 baseline-separated compounds. Combined with the results obtained from the acidic test set examined in the earlier defined strategy, of all tested compounds 82.5% showed enantioselectivity and 49.2% could be baseline-separated.


Subject(s)
Electrophoresis, Capillary/methods , Pharmaceutical Preparations/isolation & purification , Amylose/analogs & derivatives , Buffers , Cellulose/analogs & derivatives , Phenylcarbamates , Static Electricity , Stereoisomerism , Temperature
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