Persona: Monago Maraña, Olga
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Monago Maraña
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Publicación Quantification of soluble solids and individual sugars in apples by Raman spectroscopy: A feasibility study(Elsevier, 2021-06-08) Afseth, Nils Kristian; Knutsen, Svein Halvor; Wubshet, Sileshi Gizachew; Wold, Jens Petter; Monago Maraña, OlgaThis study reports the feasibility of using Raman spectroscopy for quantification of soluble solids and individual sugars in apples. Six different commercial apple varieties were measured by Raman spectroscopy at three different steps: 1) Intact apples with skin, 2) apples without skin and 3) juices obtained from apples. Results indicated that it is possible to measure Raman signals to a depth of 8 mm into the apple with a wide area Raman probe. Multivariate calibration models were established to evaluate how well Raman spectra can be used to estimate the quality parameters SSC (%), total sugars, glucose, fructose and sucrose. Estimation accuracy for SSC was comparable with what is achievable with near-infrared spectroscopy: Root mean square error of cross-validation (RMSECV) = 0.66, 0.46 and 0.72 % and coefficients of determination (R2) = 0.70, 0.85 and 0.63 for intact apples, apples without skin and juices, respectively. Sucrose and glucose were well estimated with RMSECV of 2.8, 1.9, 2.1 mg/mL for glucose and 5.8, 3.9 and 3.7 mg/mL for sucrose, for the three sample cases, respectively. Coefficient of determination was higher than 0.82 for all models. Regression coefficients for all calibration models highlighted identifiable Raman bands that could be related to the target sugars.Publicación Untargeted classification for paprika powder authentication using visible – Near infrared spectroscopy (VIS-NIRS)(Elsevier, 2021-03) Eskildsen, Carl Emil; Galeano Díaz, Teresa; Muñoz de la Peña, Arsenio; Wold, Jens Petter; Monago Maraña, OlgaThis paper describes a non-destructive screening method for authentication of paprika belonging to the Spanish Protected Designation of Origin (PDO) “Pimentón de La Vera”. Different multivariate classification models were developed in order to differentiate PDO and non-PDO samples, using visible-near infrared spectra as fingerprint for each paprika sample. Sample treatment was not required. Principal component analysis (PCA) was applied in different spectral ranges: 400–2500, 400–800 and 800–2500 nm. In all spectral ranges, PCA was largely able to differentiate PDO from non-PDO samples. Partial least-squares - discriminant analysis (PLS-DA), PCA-linear discriminant analysis (LDA) and PCA-quadratic discriminant analysis (QDA) were used as classification methods in the different spectral ranges. All methods were able to differentiate PDO from non-PDO samples, with error rates (ER) lower than 0.15. The best models were those obtained with PLS-DA in the NIR range (800–2500 nm), showing ERs lower than 0.07 and error indexes (IERROR) (false positives) lower than 0.05.Publicación Non-destructive fluorescence spectroscopy combined with second-order calibration as a new strategy for the analysis of the illegal Sudan I dye in paprika powder(Elsevier, 2020-05) Eskildsen, Carl Emil; Muñoz de la Peña, Arsenio; Galeano Díaz, Teresa; Wold, Jens Petter; Monago Maraña, OlgaThis paper presents a novel strategy for determination of the illegal dye Sudan I in paprika powder. The method is based on fluorescence spectroscopy combined with second-order calibration, which was employed for the first time for this purpose. The method is non-destructive and requires no sample preparation. It was probed that Sudan I exhibited fluorescence; however, the color of paprika samples affected the signal and it was not possible to quantify this adulterant by means of univariate and first-order calibration. To model the effect of variability of color in samples, a central composite experimental design was performed with varying ASTA (American Spices Trade Association) color values and Sudan I concentrations. Different second-order algorithms were tried for quantification. The best results for calibration and validation were obtained from Unfolded-Partial Least-Squares (U-PLS) and Multi-way Partial Least-Squares (N-PLS). The level of detection ranges were 0.4 – 3 mg/g and 0.5 – 3 mg/g for U-PLS and N-PLS, respectively. This was lower than other methods found in the literature.