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<dc:title>Detection of Nutrients and Contaminants in the Agri-Food Industry Evaluating the Probabilities of False Compliance and False Non-Compliance Through PLS Models and NIR Spectroscopy</dc:title>
<dc:creator>Castro Reigía, David</dc:creator>
<dc:creator>García, Iker</dc:creator>
<dc:creator>Sanllorente Méndez, Silvia</dc:creator>
<dc:creator>Ortiz Fernández, Mª Cruz</dc:creator>
<dc:creator>Sarabia Peinador, Luis Antonio</dc:creator>
<dc:subject>PLS Calibration</dc:subject>
<dc:subject>NIR Spectroscopy</dc:subject>
<dc:subject>Contaminants</dc:subject>
<dc:subject>Food adulterants</dc:subject>
<dc:subject>Capability of detection</dc:subject>
<dc:subject>Minimun detectable concentration</dc:subject>
<dc:subject>False positive</dc:subject>
<dc:subject>False negative</dc:subject>
<dc:subject>False compliance</dc:subject>
<dc:subject>False non-compliance</dc:subject>
<dc:description>NIR spectroscopy has become one of the most prominent techniques in the food industry due to its easy and fast use. Coupled with PLS, it is a well-established method for determining nutrients, contaminants, or adulterants in foods. Nevertheless, it is not common when calculating the capability of detection or discrimination given a target/permitted value, providing probabilities of false non-compliance (α) or false compliance (β). That is exactly the main purpose of this work, where a single procedure using the accuracy line to evaluate these figures of merit by generalizing ISO 11843 when using NIR-PLS in real scenarios in agri-food industries is shown. Nevertheless, it is a completely general procedure and can be used in any analytical context in which a PLS calibration is applied. As an example of its versatility, several analytical determinations were performed using different common food matrices in the agri-food industry (butter, flour, milk, yogurt, oil, and olives) for the quantification of protein, fat, salt, and two agrochemicals. Some results were a detection capability of 5.2% of fat in milk, 1.20 mg kg−1 for diflufenican, and 2.34 mg kg−1 for piretrin in olives when maximum limits were established at 5%, 0.6 mg kg−1, and 0.5 mg kg−1 respectively. Also, 1.02% for salt in butter and 11.45%, 3.78%, and 2.65% for protein in flour, milk, and yogurt, respectively, were obtained when minimum limits were established at 1.2%, 12%, 4%, and 3% respectively. In all cases α = β = 0.05.</dc:description>
<dc:date>2025-05-13T06:24:37Z</dc:date>
<dc:date>2025-05-13T06:24:37Z</dc:date>
<dc:date>2025-04</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>http://hdl.handle.net/10259/10459</dc:identifier>
<dc:identifier>10.3390/app15094808</dc:identifier>
<dc:identifier>2076-3417</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>Applied Sciences. 2025, V. 15, n. 9, p. 4808</dc:relation>
<dc:relation>https://doi.org/10.3390/app15094808</dc:relation>
<dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>Atribución 4.0 Internacional</dc:rights>
<dc:publisher>MDPI</dc:publisher>
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