E. Forgacs, USE OF PRINCIPAL COMPONENT ANALYSIS FOR THE EVALUATION OF THE RETENTION BEHAVIOR OF MONOAMINE-OXIDASE INHIBITORY DRUGS ON BETA-CYCLODEXTRINCOLUMN, Journal of pharmaceutical and biomedical analysis, 13(4-5), 1995, pp. 525-532
The retention of 17 monoamine oxidase inhibitory drugs (proparlgylamin
e derivatives) were determined on a beta-cyclodextrin polymer (beta CD
P)-coated silica column using ethanol-0.05 M K2HPO4 (6:4 v/v) as the e
luent. The relative strength of interaction between the drugs and a wa
ter soluble beta-cycodextrin polymer was determined by charge-transfer
chromatography carried out on reversed-phase TLC layers. The relation
ship between capacity factors, physicochemical parameters and inclusio
n complex forming capacity of the monoamine oxidase inhibitory drugs w
ere evaluated by stepwise regrerssion analysis and by principal compon
ent analysis (PCA) followed by two-dimensional nonlinear mapping and v
arimax rotation. Calculations indicated that the retention of monoamin
e oxidase inhibitory drugs on beta CDP column is mainly governed by th
eir steric and lipophylic parameters. Significant linear correlations
were found between the corresponding coordinates of varimax rotation a
nd two-dimensional nonlinear maps proving the suitability of both meth
ods for the reduction of dimensionality of complicated data matrices.