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dc.contributor.author
Mazivila, Sarmento J.  
dc.contributor.author
Lombardi, Juan Manuel  
dc.contributor.author
Páscoa, Ricardo N. M. J.  
dc.contributor.author
Bortolato, Santiago Andres  
dc.contributor.author
Leitão, João M. M.  
dc.contributor.author
Silva, Joaquim C. G. Estevez da  
dc.date.available
2022-05-02T18:15:19Z  
dc.date.issued
2021-02-15  
dc.identifier.citation
Mazivila, Sarmento J.; Lombardi, Juan Manuel; Páscoa, Ricardo N. M. J.; Bortolato, Santiago Andres; Leitão, João M. M.; et al.; 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; Elsevier Science; Analytica Chimica Acta; 1146; 15-2-2021; 98-108  
dc.identifier.issn
0003-2670  
dc.identifier.uri
http://hdl.handle.net/11336/156251  
dc.description.abstract
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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
FAPV  
dc.subject
MCR-ALS  
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PARAFAC  
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SYNCHRONIZATION OF LC-DAD DATA  
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THREE-WAY CALIBRATION  
dc.subject.classification
Química Analítica  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
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  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2021-12-03T21:36:39Z  
dc.journal.volume
1146  
dc.journal.pagination
98-108  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Mazivila, Sarmento J.. Universidad de Porto. Facultad de Ciências; Portugal  
dc.description.fil
Fil: Lombardi, Juan Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina  
dc.description.fil
Fil: Páscoa, Ricardo N. M. J.. Universidad de Porto. Facultad de Ciências; Portugal  
dc.description.fil
Fil: Bortolato, Santiago Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina  
dc.description.fil
Fil: Leitão, João M. M.. Universidad de Coimbra; Portugal  
dc.description.fil
Fil: Silva, Joaquim C. G. Estevez da. Universidad de Porto. Facultad de Ciências; Portugal  
dc.journal.title
Analytica Chimica Acta  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.aca.2020.12.033  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0003267020312265