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Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification
Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification
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Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification
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Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification
Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification

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Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification
Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification
Journal Article

Authentication of Iranian Saffron (Crocus sativus) Using Stable Isotopes δ 13 C and δ 2 H and Metabolites Quantification

2022
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Overview
Saffron is a very high value-added ingredient used in the food supplement market and contains a high level of safranal. Adding synthetic safranal to saffron, which is significantly cheaper, and falsifying the origin of saffron may represent recurrent fraud. Saffron from different countries was analyzed to determine the stable isotope ratios δ 13 C and δ 2 H from safranal by gas chromatography coupled with isotope-ratio mass spectrometry (GC-C/P-IRMS) and the concentration of saffron metabolites with ultra-high performance liquid chromatography coupled with diode array detector (UHPLC-DAD). The isotopic analysis highlighted a higher ratio of δ 2 H in synthetic safranal than in natural safranal; the mean values were 36‰ (+/− 40) and −210‰ (+/− 35), respectively. The δ 13 C between Iranian, Spanish and other saffron was significantly different and represents median values of −28.62‰, −30.12‰ and −30.70‰, respectively. Moreover, linear and quadratic discriminant analyses (LDA and QDA) were computed using the two isotope ratios of safranal and the saffron metabolites. A first QDA showed that trans-crocetin and the δ 13 C of safranal, picrocrocin, and crocin C3 concentrations clearly differentiated Iranian saffron from other origins. A second model identified δ 13 C, trans-crocetin, crocin C2, crocin C3, and picrocrocin as good predictors to discriminate saffron samples from Iran, Spain, or other origins, with a total ability score classification matrix of 100% and a prediction matrix of 82.5%. This combined approach may be a useful tool to authenticate the origin of unknown saffron.