Validation of a high-throughput method for the accurate quantification of secondary products of lipid oxidation in high-quality hazelnuts (Corylus avellana L.): A robust tool for quality assessment

被引:8
作者
Squara, Simone [1 ]
Caratti, Andrea [1 ]
Ortega Gavilan, Fidel [2 ]
Bolzoni, Paola [1 ]
Spigolon, Nicola [3 ]
Genova, Giuseppe [3 ]
Castello, Giuseppe [3 ]
Bagur Gonzalez, Maria Gracia [2 ]
Cuadros-Rodriguez, Luis [2 ]
Bicchi, Carlo [1 ]
Cordero, Chiara [1 ]
机构
[1] Univ Torino, Dipartimento Sci & Tecnol Farmaco, Via Pietro Giuria 9, I-10125 Turin, Italy
[2] Univ Granada, Dept Analyt Chem, Fac Sci, Ave Fuentenueva S-N, E-18071 Granada, Spain
[3] Soremartec Italia Srl, Piazzale Ferrero 1, I-12051 Alba, Cuneo, Italy
关键词
Corylus avellana L; Secondary products of lipid oxidation; Linear saturated aldehydes; Quality control; Rancidity; Accurate quantification; Method validation; GENTILE TRILOBATA HAZELNUTS; FATTY-ACIDS; GAS-CHROMATOGRAPHY; AUTHENTICATION; IDENTIFICATION; EXTRACTION; GC; QUANTITATION; STABILITY; ORIGIN;
D O I
10.1016/j.jfca.2022.104766
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
European hazelnuts (Corylus avellana L.) are a key ingredient for the confectionery industry with a distinctive flavor profile and high nutritional quality. However, the high-fat content makes raw kernels prone to autoxidation that takes place during storage. Fatty acids hydroperoxides (i.e., primary products of oxidation) readily decompose by forming volatile secondary products with low odor thresholds and negative aroma notes. This study presents method performance parameters of an accurate quantitative methodology, based on multiple headspace solid-phase microextraction (MHS-SPME) coupled to conventional and fast gas chromatography-mass spectrometry ((Fast)GC-MS), targeted to oleic and linoleic acids autoxidation products (i.e., hexanal, heptanal, octanal, and nonanal). Results refer to good repeatability (max RSDr 12%) and intermediate precision (max RSDR 19.6%); linearity over four orders of magnitude (R-2 >= 0.995 and calibration error <= 20%); good accuracy (error bias <= 20%); limit of detection and quantification compatible with real-world samples oxidative levels. Experimental results from method application on 358 industrial samples, confirm the method's effectiveness and its information capacity; moreover, for medium-to-high oxidized samples, the quantification of a larger set of products instead of a single marker (i.e., hexanal), provides a more accurate picture on the actual quality/rancidity level.
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页数:11
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