METHOD DEVELOPMENT IN PHARMACEUTICAL ANALYSIS EMPLOYING CAPILLARY ELECTROCHROMATOGRAPHY

Citation
Pda. Angus et al., METHOD DEVELOPMENT IN PHARMACEUTICAL ANALYSIS EMPLOYING CAPILLARY ELECTROCHROMATOGRAPHY, Electrophoresis, 19(12), 1998, pp. 2073-2082
Citations number
42
Categorie Soggetti
Biochemical Research Methods","Chemistry Analytical
Journal title
ISSN journal
01730835
Volume
19
Issue
12
Year of publication
1998
Pages
2073 - 2082
Database
ISI
SICI code
0173-0835(1998)19:12<2073:MDIPAE>2.0.ZU;2-2
Abstract
Capillary electrochromatography (CEC) has been employed to explore met hod development for a series of structurally related polar neutral com pounds of pharmaceutical relevance. Capillaries with dimensions of 75 mu m ID x 25 cm length (34.5 cm total) were packed with Spherisorb ODS -1, Hypersil phenyl, and Hypersil MOS (all 3 mu m particles) and were compared in the reversed-phase mode in order to determine which phase provided the best initial performance and thus serve as the phase of c hoice for additional method development experiments. The various separ ation parameters examined for their effect on efficiency, k', resoluti on, and linear velocity included percent and type of organic modifier, buffer concentration, voltage, and temperature. All separations were conducted with an acidic mobile phase (aqueous mobile phase component, pH 3.0). The separation efficiencies obtained were on the order of 20 0 000-260 000 plates/m, which equates to reduced plate heights of 1.22 for columns packed with Spherisorb, ODS-1. Repeatable column-to-colum n separation performance was demonstrated.