Matteo Perini, Silvia Pianezze, Laura Pienti, Giovanna Randi, Pietro Franceschi, Roberto Larcher
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l(+)-tartaric acid of grape origin: Definition of threshold limits for the 13C/12C and 18O/16O stable isotope ratios and validation of the isotopic method through an interlaboratory study.
l(+)-tartaric acid is one of the most used additives in the oenological practices. Its properties make it useful as preservative and acidulant in grape-derived products. This additive can be obtained through the extraction from grapes, from other fruits or through synthesis from petrochemical sources. In Europe, only l(+)-tartaric acid from grapes can be added to wine products, but the price difference between the forms could lead to the fraudulent use of the cheaper synthetic l(+)-tartaric acid. In other continents where such limitation is not applied, the clear commercial identification of the products is still desirable. Stable isotope analysis of carbon (δ13C) and oxygen (δ18O) proved to be a robust and effective method in discriminating between synthetic and grape-derived l(+)-tartaric acid. In this study, to define the threshold limits of δ13C (above -24.8 ‰) and δ18O (above +25.6 ‰) of grape-derived l(+)-tartaric acid, a database consisting of 81 authentic natural samples was created. Moreover, the validation of the isotopic method through an interlaboratory study involving nine European and extra-European laboratories, was provided. The repeatability and the reproducibility standard deviation of the method were calculated.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.