Three-way calibration using PARAFAC and MCR-ALS with previous synchronization of second-order chromatographic data through a new functional alignment of pure vectors for the quantification in the presence of retention time shifts in peak position and shape.

In the present contribution is shown the application of the recently developed functional alignment of pure vectors (FAPV) as a proper algorithm to align second-order chromatographic data with severe retention time shifts in peak position and shape. FAPV decomposed a three-way chromatographic data array in their three modes (sample, spectral and elution time vectors), using a basis function to pre-process the non-linear mode (elution time) and then it aligns the functionalized pure vectors and reshapes the transformed vectors into matrices, restoring the trilinearity of second-order chromatographic data. The well-aligned three-way chromatographic data array is then successfully decomposed by advanced chemometric models such as parallel factor analysis (PARAFAC) and multivariate curve resolution - alternating least-squares (MCR-ALS) with the trilinearity constraint. The performance of this innovative analytical strategy based on PARAFAC and MCR-ALS with previous synchronization of data through FAPV algorithm is properly evaluated using real second-order chromatographic data with multiple artifacts, i.e., shifts in peak position and shape for the simultaneous quantification of amoxicillin and potassium clavulanate in commercial medicinal drugs. The present contribution compares some analytical results achieved by: (1) the usual MCR-ALS as a bilinear model applied in augmented data matrix without previous synchronization and with interval correlation optimized shifting (ICOSHIFT) and FAPV and (2) trilinear models using PARAFAC with ICOSHIFT and FAPV and trilinearity constraint in MCR-ALS with FAPV. Available results suggest that these strongly shifted and warped elution time profiles cause for the loss of trilinearity, which can be adequately restored by FAPV algorithm. PARAFAC performed a successful trilinear decomposition of three-way chromatographic data array with law values of relative prediction error (REP) in the order of 1.34-1.42% in both analytes.