Tidsskrift: Journal of Food Science, vol. 69, p. E417–E421, 2004
Publikasjonstype: Vitenskapelig artikkel
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Filleting byproducts (heads, frame bones, skin, and down-graded gutted fish) from farmed Atlantic salmon (Salmo salar) were separated into a solid/aqueous phase and a lipid phase (oil) using a scraped-surface heat exchanger (90 degreesC to 95 degreesC) and a decanter centrifuge (93 degreesC). Effects of storage temperature (4 degreesC and 23 degreesC), atmosphere (air and N-2), and time (0 to 180 d), as well as an additional process step-a separator introduced after the decanter centrifuge, were investigated on the quality and storage stability of the produced on. Samples were analyzed for the quality parameters peroxide (PV), anisidine (AV), and Totox value (TxV), content of free fatty acids (FFA), content of fatty acid methyl esters (FAME), especially the n-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) and degradation of EPA and DHA related to the content of hexadecanoic acid (HDA) (ratios EPA/HDA and DHA/HDA). Storage temperature had significant effect on all the investigated quality parameters, especially on AV, PV, and TxV where a high storage temperature (23 degreesC) caused a 10-fold, 2.5-fold, and 4-fold increase in AV, PV, and TxV, respectively. Storage atmosphere had significant effect on all the investigated parameters, except on the DHA/HDA ratio, where storage under an N-2 atmosphere significantly preserved the quality of the oil compared with storage in air. Generally, no significant effect of storage time on the investigated quality parameters was observed before 120 d of storage. No effect on quality was observed when introducing an additional processing step (separator) after the decanter centrifuge. Salmon oil is a stable product, and even more so when stored at appropriate conditions (under nitrogen atmosphere at refrigerated temperatures).