Rapid and nondestructive identification of Belgian and Netherlandish trappist beers by front-face synchronous fluorescence spectroscopy coupled with multiple statistical analysis

Main Article Content

Jin Tan Tianjin Key Laboratory of Food Biotechnology, College of Biotechnology and Food Science, Tianjin University of Commerce, Tianjin 300134, People’s Republic of China.
Ming-Fen Li Tianjin Key Laboratory of Food Biotechnology, College of Biotechnology and Food Science, Tianjin University of Commerce, Tianjin 300134, People’s Republic of China.

Keywords

front-face fluorescence, linear discriminant analysis (LDA), partial least squares-discriminant analysis (PLS-DA), principal component analysis (PCA), Trappist beers

Abstract

Front-face synchronous fluorescence spectroscopy (FFSFS) was applied for the rapid and noninvasive recognition of Belgian and Netherlandish Trappist beers against non-Trappist beers. The front-face synchronous fluorescence spectra at wavelength intervals (Δλ) of 30 and 60 nm for 80 bottles of beer, including 41 Trappist and 39 non-Trappist beers, were acquired in a 5 × 10 mm fused-quartz cuvette settled in a traditional right-angle sample compartment. The discrimination model was constructed by either principal component analysis (PCA) combined with linear discriminant analysis (LDA) or partial least squares-discriminant analysis (PLS-DA). Both PCA–LDA and PLS-DA models were validated by full (leave-one-out) cross-validation and k-fold cross-validation (k = 5). The PCA–LDA model presents reliable discrimination performance, with the cross-validated sensitivity (true positive rate) and specificity (true negative rate) in the range of 82.9–85.4% and 71.8–76.9%, respectively. The misclassification mainly occurs to a small portion of ambiguous Trappist and non-Trappist samples such as Abbey beers, which are rather similar to Trappist beers.

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