Author/Authors :
Pellett، نويسنده , , Jackson and Lukulay، نويسنده , , Patrick and Mao، نويسنده , , Yun and Bowen، نويسنده , , William and Reed، نويسنده , , Robert and Ma، نويسنده , , M. and Munger، نويسنده , , R.C. and Dolan، نويسنده , , J.W. and Wrisley، نويسنده , , Loren and Medwid، نويسنده , , K. and Toltl، نويسنده , , N.P. and Chan، نويسنده , , C.C. and Skibic، نويسنده , , M. and Biswas، نويسنده , , Kallol and Wells، نويسنده , , Kevin A. and S، نويسنده ,
Abstract :
A general procedure is proposed for the rapid development of a reversed-phase liquid chromatographic (RP-LC) separation that is “orthogonal” to a pre-existing (“primary”) method for the RP-LC separation of a given sample. The procedure involves a change of the mobile-phase organic solvent (B-solvent), the replacement of the primary column by one of very different selectivity, and (only if necessary) a change in mobile phase pH or the use of a third column. Following the selection of the “orthogonal” B-solvent, column and mobile phase pH, further optimization of peak spacing and resolution can be achieved by varying separation temperature and either isocratic %B or gradient time. The relative “orthogonality” of the primary and “orthogonal” RP-LC methods is then evaluated from plots of retention for one method versus the other.
esent procedure was used to develop “orthogonal” methods for nine routine RP-LC methods from six pharmaceutical analysis laboratories. The relative success of this approach can be judged from the results reported here.