The present study was designed to assess the effect of local canning process and storage time (up to 6 months) on tuna and sardine canned in olive oil and tomato sauce, respectively. The canning process affected tuna (P < 0.05) but not sardine lipid levels. Canned tuna and sardine absorbed coating oil during sterilization, inducing a higher oleic (C18:1 w9) and linoleic (C18:2 w6) acid content. Independent of fish species, the eicosapentaenoic (C20:5 w3) and docosahexaenoic (C22:6 w3) acid concentrations ranged from 2.96-6.24% and from 5.16-40.26%, respectively. The peroxide value and thiobarbituric acid index increased significantly in tuna but not in sardine flesh following the cooking step. The histamine levels increased significantly (P < 0.05) during storage but remained lower than the threshold limits. Although tuna and sardine flesh were slightly affected by the canning process, they remained good sources of w3 and w6 fatty acids. PRACTICAL APPLICATIONSIn the present study, we investigate the changes of the lipid fraction quality (fatty acids composition, peroxide value and thiobarbituric acid index) and histamine during processing and storage of two different fish species (tuna and sardine) processed during the same period. This would allow for the 3 Corresponding

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This study aimed to produce new value‐added products from dolphinfish ( Coryphaena hippurus ) as fillets when using cold smoking combined with natural antioxidants, obtained from Halocnemum strobilaceum a plant belonging to halophytes. The fillet treatments were controlled (untreated), immersed in standard brine ( STD ), treated with Na CI and antioxidant before freezing (Aox‐pre) and treated with NaCl and antioxidant after thawing (Aox‐post). The quality of dolphinfish fillets was assessed using sensory, biochemical, microbiological, and technological parameters. Treating fillets with antioxidants before freezing and cold smoking (Aox‐pre) enhanced significantly the shelf life, as well as improved the biochemical, microbiological, and sensory aspects of the product. Aox‐pre fillets had the lowest peroxide values ( PV ) and malondialdehyde ( MDA ) content, demonstrating that the immediate treatment of fillets with the polyphenols protected lipids from peroxidation. The smoking process, together with antioxidant treatment, significantly reduced microbial counts after 15 days of storage, compared to the control. Overall, combining antioxidant treatments with cold smoking has a positive effect on the quality of Aox‐pre fillets with respect to both sensory components and biochemical parameters associated with shelf life. Consequently, Aox‐pre treatment enhances the marketability of this species, promoting local and seasonal products, contributing to costal fisheries sustainability.

The acid solubilised collagen (ASC) and pepsin solubilised collagen (PSC) were extracted from the by-products (skin) of a cartilaginous fish (Mustelus mustelus). The ASC and PSC yields were 23.07% and 35.27% dry weight, respectively and were identified as collagen Type I with the presence of α, β and γ chains. As revealed by the Fourier Transform Infrared (FTIR) spectra analysis, pepsin did not alter the PSC triple helix structure. Based on the various type of collagen yield, only PSC was used in combination with chitosan to produce a composite film. Such film had lower tensile strength but higher elongation at break when compared to chitosan film; and lower water solubility and lightness when compared to collagen film. Equally, FTIR spectra analysis of film composite showed the occurrence of collagen-chitosan interaction resulting in a modification of the secondary structure of collagen. Collagen-chitosan-based biofilm showed a potential UV barrier properties and antioxidant activity, which might be used as green bioactive films to preserve nutraceutical products.

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