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[Display omitted] • First observation of fluorescence quenching between solid foods. • Fluorescence quenching is proven to be induced by competitive absorption. • Competitive absorption occurs between phenolic acids and curcumin. • Fast and non-invasive analysis of maize flour in turmeric powder by FFSFS and PLS. • FFSFS offers a new strategy for composition analysis of solid food blends. Fluorescence quenching induced by competitive absorption between different components of solid foods was observed for the first time. By using front-face synchronous fluorescence spectroscopy (FFSFS) and fluorescence titration, competitive absorption between maize flour and turmeric powder was proven to occur between phenolic acids in maize flour and curcumin in turmeric powder. FFSFS was applied for the rapid and non-destructive determination of maize flour adulterated in turmeric powder. Prediction models were constructed by partial least square (PLS) regression based on unfolded total synchronous fluorescence spectra, and were validated by five-fold cross-validation and external validation, with the determination coefficient of prediction (R p 2) greater than 0.95, root mean square error of prediction (RMSEP) < 6%, relative error of prediction (REP) < 15% and residual predictive deviation (RPD) greater than 5. The limit of detection (LOD) of maize flour was approximately 9%. In addition, most relative errors for test samples were from −20% to 20%. [ABSTRACT FROM AUTHOR]

Quinoa is a naturally gluten-free pseudocereal receiving growing attentions worldwide. Herein, front-face synchronous fluorescence spectroscopy (FFSFS) was applied for the fast and non-invasive authentication of quinoa flour adulteration with maize and soybean flours. The cases of both single and dual adulterants (6–50 wt%) were investigated. For single adulteration with either maize or soybean flour, principal component analysis coupled with linear discriminant analysis (PCA–LDA) was used for preliminary qualitative discrimination. Then first-order prediction models were constructed based on the combination of unfolded total synchronous fluorescence spectra and partial least square (PLS) regression, and were validated by five-fold cross-validation and external validation. For dual adulterants, a general PLS2 model for the simultaneous determination of maize and soybean flours was developed, which produced suitable results, with the determination coefficient of prediction (R p 2) > 0.9, root mean square error of prediction (RMSEP) < 5% and residual predictive deviation (RPD) > 3. The limits of detection (LODs) are 9.0% and 6.9% for maize flour and soybean flour, respectively. Furthermore, most spike recoveries are in the range of 80–120%. This study not only has important applications in the authentication of quinoa flour adulteration but may also shed light on the quantitative component analysis of other cereal flour mixtures from different botanical origins. • Front-face synchronous fluorescence of quinoa flour is presented. • Its emission is distinct from those of maize and soybean flours. • Quinoa flavonoids contribute most to the distinction, followed by tryptophan. • Front-face fluorescence affords non-destructive detection of its adulteration. • Simultaneous determination of maize and soybean flours can be rapidly achieved. [ABSTRACT FROM AUTHOR]

The authentication of traditional herbal medicines in powder form is of great significance, as they are always of high values but vulnerable to adulteration. Based on the distinct fluorescence of protein tryptophan, phenolic acids and flavonoids, front-face synchronous fluorescence spectroscopy (FFSFS) was applied for the fast and non-invasive authentication of Panax notoginseng powder (PP) adulterated with the powder of rhizoma curcumae (CP), maize flour (MF) and whole wheat flour (WF). For either single or multiple adulterants in the range of 5–40% w /w, prediction models were built based on the combination of unfolded total synchronous fluorescence spectra and partial least square (PLS) regression, and were validated by both five-fold cross-validation and external validation. The constructed PLS2 models simultaneously predicted the contents of multiple adulterants in PP and gave suitable results, with most of the determination coefficients of prediction (R p 2) >0.9, the root mean square error of prediction (RMSEP) no >4% and residual predictive deviation (RPD) >2. The limits of detections (LODs) were 12.0, 9.1 and 7.6% for CP, MF and WF, respectively. All the relative prediction errors for simulated blind samples were between −22% and + 23%. FFSFS offers a novel alternative to the authentication of powdered herbal plants. [Display omitted] • Front-face fluorescence of Panax notoginseng powder is observed and utilized. • Simultaneous detection of multiple adulterants in Panax notoginseng powder by PLS2. • Protein tryptophan, phenolic acids and flavonoids contribute to the detection. • Front-face fluorescence affords rapid and non-destruction drug authentication. [ABSTRACT FROM AUTHOR]