IQUIR   05412
INSTITUTO DE QUIMICA ROSARIO
Unidad Ejecutora - UE
artículos
Título:
Novel Augmented Parallel Factor Model for Four-Way Calibration of High-Performance Liquid Chromatography-Fluorescence Excitation-Emission Data
Autor/es:
BORTOLATO, SANTIAGO ; LOZANO, VALERIA A.; MUÑOZ DE LA PEÑA, ARSENIO; OLIVIERI, ALEJANDRO C.
Revista:
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS
Editorial:
ELSEVIER SCIENCE BV
Referencias:
Lugar: Amsterdam; Año: 2015 vol. 141 p. 1 - 11
ISSN:
0169-7439
Resumen:
A newaugmented parallel factor analysismodel (Augmented PARAFAC) is presented, inspired by the useful augmentation concept employed inmultivariate curve resolution-alternating least-squares(MCR-ALS), applicable to calibration based on non-quadrilinear four-way data, such as those produced by high-performance liquid chromatographywith matrix excitation?emission fluorescence detection. The new model involves creating an augmented three-way array in the elution time direction, containing data for the calibration sample set and for each of the test samples, subsequently analyzed with an Augmented PARAFAC version. To test the properties of this approach, chromatographic data were simulated with different degrees of overlapping and misalignment among the chromatographic peaks. Additionally, experimental data from olive oil samples were tested with the new model, aimed at the quantitation of the level of chlorophylls and pheophytins. The results were compared with those obtained by data processing with MCR-ALS. Relative prediction errors (%) were: Augmented PARAFAC, 9.7, 21.0, 14.7 and 9.3, andMCR-ALS, 5.9, 14.5, 20.0 and 14.7 for Chl a, Chl b, Phe a Phe b, respectively,for concentrations in the range 0.00-1.00 μgmL−1. BothMCR-ALS and Augmented PARAFAC allowone to obtain a detailed and realistic description of the analyzed samples, in terms of pure elution time, excitation and emission spectral profiles, which can be independently retrieved for every component.