Effect of combined chitosan-krill oil coating and modified atmosphere packaging on the storability of cold-stored lingcod (Ophiodon elongates) fillets

Chitosan solutions (3%) incorporating 20% krill oil (w/w chitosan) with or without the addition of 0.1 μl/ml cinnamon leaf essential oil were prepared. Fresh lingcod (Ophiodon elongates) fillets were vacuum-impregnated with the coating solutions, vacuum or modified atmosphere (MA) (60% CO₂ + 40% N₂) packaged, and then stored at 2 °C for up to 21 days for physicochemical and microbial quality evaluation. Chitosan-krill oil coating increased total lipid and omega-3 fatty acid contents of the lingcod by about 2-fold. The combined chitosan coating and vacuum or MA packaging reduced lipid oxidation as represented in TBARS, chemical spoilage as reflected in TVBN, and microbiological spoilage as reported in total plate count (2.22–4.25 Log reductions during storage). Chitosan-krill oil coating did not change the colour of the fresh fillets, nor affect consumers’ acceptance of both raw and cooked fish samples. Consumers preferred the overall quality of chitosan-coated, cooked lingcod samples over the control, based on their firm texture and less fishy aroma.     

Effect of chitosan-based solutions applied as edible coatings and water glazing on frozen salmon preservation – A pilot-scale study

The aim of this research was to compare the effect of chitosan solutions on frozen salmon preservation with that of water glazing. For this purpose, three chitosan solutions (0.25%, 0.50% and 0.75% w/v) and water were applied in different amounts (6%, 8% and 11% of coated fillet weight) directly on the surface of frozen salmon. In order to accelerate the deterioration processes, salmon was stored during 14 weeks at −5 °C. Microbial and chemical indices were used to assess deterioration during storage and the coating stability was evaluated through weight loss measurements. The results obtained showed that chitosan coatings can be a good barrier to protect frozen fish from deterioration. Microbial growth, assessed by total viable counts (TVC), and total volatile basic nitrogen (TVB-N) were maintained below the maximum limits recommended which are 5 × 105 CFU/g and 35 mg nitrogen/100 g fish, respectively. The use of 0.50% and 0.75% chitosan solutions generally demonstrated to be more efficient in preventing salmon weight loss.     

Effects of chitosan coating on quality and shelf life of silver carp during frozen storage

The effects of chitosan coating on quality and shelf life of silver carp during frozen storage were investigated. Fish samples were treated with aqueous solution of 2% chitosan, and then stored at −3 °C for 30 days. The control and the treated fish samples were analyzed periodically for microbiological (total viable count), chemical (pH, TBA, TVB-N, K-value), and sensory characteristics. The results indicated that the effect of chitosan coating on fish samples was to retain their good quality characteristics and extend the shelf life during frozen storage, which was supported by the results of microbiological, chemical, and sensory evaluation analyses.     

Effects of chitosan coating enriched with cinnamon oil on qualitative properties of sweet pepper (Capsicum annuum L.)

Effect of chitosan–oil coating on qualitative properties of sweet pepper (Capsicum annuum L.) stored at 8 °C for 35 days was investigated. The chitosan–oil coating treatment exhibited the best control effect on decay (below 5%). At the end of storage, samples treated with chitosan-oil coatings maintained good sensory acceptability, whereas the sensory quality of control samples became unacceptable. The higher activities of scavenger antioxidant enzymes, including superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT), in treated peppers at the 35th day should be contributed to the chitosan–oil coating. Malondialdehyde (MDA) and electrolyte leakage contents in chitosan–oil-coated peppers were increased but were still lower than in control samples. Atomic force microscopy images showed that the surface of sweet pepper without coating treatment was rougher than that of peppers treated with chitosan–oil coating. Our study suggests that chitosan–oil coating might be a promising candidate for enhancing the keeping quality of sweet peppers.     

Stability of encapsulated olive oil in the presence of caffeic acid

The aim of this study was to investigate the influence of microencapsulation and addition of the phenolic antioxidant caffeic acid (CA) on the storage stability of olive oil. Olive oil in the absence or presence of 300 ppm CA was encapsulated in 1.5% w/w sodium alginate shells. Encapsulated oil (with/without added CA) and unencapsulated oil were stored at 20 or 37 °C for 30 days and then subjected to stability and quality evaluation based on peroxide value (PV), p-anisidine value (p-AV), Totox value, free fatty acid (FFA), total extractable phenolic content (TEPC), and fatty acid composition. The CA addition increased the stability and TPC of the final oil product. Oxidation changes were generally slower in the encapsulated oil samples. Both encapsulation and addition of CA preserved unsaturated fatty acids (UFAs) including C18:1 (omega-9 FA), C18:2 (omega-6 FA) and C18:3 (omega-3 FA). We conclude that the current oil encapsulation method using alginate microspheres could be a feasible approach to increasing olive oil stability. The addition of CA to olive oil not only provides additional protection to the oil, but also improves the nutritional values of the final oil product in terms of elevated TEPC and desired UFAs.     

Effect of chitosan coatings enriched with cinnamon oil on the quality of refrigerated rainbow trout

The effects of a chitosan (Ch) coating enriched with cinnamon oil (Ch + C) on quality of rainbow trout (Oncorhynchus mykiss) during refrigerated storage (4 ± 1 °C) were examined over a period of 16 days. A solution of Ch (2%, w/v) and Ch + C (2%, w/v Ch + 1.5%, v/v C) was used for the coating. The control and the coated fish samples were analysed periodically for microbiological (total viable count, psychrotrophic count), chemical (TVB-N, PV, TBA), and sensory (raw and cooked fish) characteristics. The results indicated that the effect of the Ch + C coating on the fish samples was to enable the good quality characteristics to be retained longer and to extend the shelf life during the refrigerated storage.     

Physicochemical characterisation and oxidative stability of fish oil and fish oil–extra virgin olive oil microencapsulated by sugar beet pectin

Spray-dried microcapsules were prepared at 25% and 50% w/w oil load from sugar beet pectin-stabilised emulsions (pH 3) containing fish oil, and a blend of fish oil and with extra virgin olive oil (1:1 w/w). Microencapsulation efficiencies were high (≥90%). However, deterioration in microcapsule wall integrity and an increase in oil droplet size were observed during storage (25 °C, 0–3 months). Lipid oxidation increased with both increased oil load (P < 0.05) and storage duration (P < 0.05), but was independent of oil composition (P > 0.05). These results suggest that sugar beet pectin functions poorly as a wall material and its residual metal ions exacerbate omega-3 oxidation, despite the presence of endogenous antioxidants found in extra virgin olive oil. Interestingly, under accelerated storage conditions (OxiPres® at 80 °C, 0.5 bar oxygen pressure), microcapsules containing the oil blend showed the best oxidative stability (P < 0.05), irrespective of oil load. A possible explanation for the superior oxidative stability of the microencapsulated oil blend at high storage temperature is discussed.     

Fatty acid compositions of fish oil extracted from different parts of Indian mackerel (Rastrelliger kanagurta) using various techniques of supercritical CO2 extraction

Fatty acid compositions of fish oil extracted from different parts of Indian mackerel (Rastrelliger kanagurta) using various techniques of supercritical carbon dioxide (SC-CO₂) at optimised conditions (35 MPa, 60 °C, 2 ml/min) were analysed and compared to the results of Soxhlet extraction. The amount of polyunsaturated fatty acids (PUFA) recovered (as a percentage of total extracted fatty acids) were within the ranges of 73.24–74.68% in the skin, 68.36–69.37% in the flesh, 56.20–57.3% in the viscera and 61.21–62.09% in the heads. The greatest amount of the ω-3 fatty acids, especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), were found in fish skin followed by flesh, heads and viscera. The greatest amounts of EPA (9–12%) and DHA (10–14%) were obtained using the soaking and pressure swing techniques. The pressure swing and soaking techniques are the most effective techniques for extracting the ω-3 family of fatty acids from fish samples.     

Fish oil in feeds for entire male and female pigs: Changes in muscle fatty acid composition and stability of sensory quality

A total of 72 crossbred [(Norwegian Landrace × Yorkshire) × Duroc] male and female growing-finishing pigs were restrictedly fed diets containing fish oil to study the fatty acid composition of Musculus longissimusdorsi and sensory quality of belly and neck. Six diets were used: two low-fat diets with or without 0.5% fish oil added, and four medium-fat diets with palm kernel oil to fish oil in ratios given as % inclusion: 4.1:0.0, 3.9:0.3, 3.6:0.5 and 3.4:0.7. Feeding fish oil gave a dose-dependent response between fatty acids in the diets and in the M.longissimusdorsi and increased the level of very long chain n−3 fatty acids, especially the C22:5n−3 (DPA). A more efficient n−3 fatty acids deposition was obtained when given as a medium-fat diet rather than the low-fat diet. Female pigs had a significant higher percentage of monounsaturated fatty acids and C18:1 than males suggesting a gender related difference in the delta-9-desaturase activity. No significant differences were found in sensory attributes for short-term stored neck and belly. For pigs fed the highest level of fish oil (0.7%) long-term stored (12 months at −80 °C, 6 months at −20 °C) belly showed a slight increase in fish oil flavour. After warmed-over treatment, fish oil odour and flavour as well as rancid flavour were increased in this group. The results suggest levels of dietary fish oil up to 0.5% produce a healthier meat fatty acid composition, without negative effects on sensory attributes, even in long-termed stored belly.     

Effect of chitosan coating combined with postharvest calcium treatment on strawberry (Fragaria × ananassa) quality during refrigerated storage

Strawberries (Fragaria × ananassa Duch.) were coated with either 1% or 1.5% chitosan (CS) or chitosan combined with calcium gluconate (CaGlu). Following treatment, strawberries were stored at 10 °C and 70 ± 5% RH for one week. The effectiveness of the treatments in extending fruit shelf-life was evaluated by determining fungal decay, respiration rate, quality attributes and overall visual appearance. No sign of fungal decay was observed during the storage period for fruit coated with 1.5% CS (with or without the addition of CaGlu) or 1% CS + 0.5% CaGlu. By contrast, 12.5% of the strawberries coated with 1% CS lacking calcium salt were infected after five days of storage. The chitosan coating reduced respiration activity, thus delaying ripening and the progress of fruit decay due to senescence. Chitosan coatings delayed changes in weight loss, firmness and external colour compared to untreated samples. Strawberries coated with 1.5% chitosan exhibited less weight loss and reduced darkening than did those treated with 1% chitosan, independently of the presence or absence of CaGlu. However, addition of calcium to the 1% chitosan solution increased the firmness of the fruit. Coated samples had greater visual acceptability than had untreated fruits. The addition of calcium gluconate to the chitosan coating formulation increased the nutritional value by incrementing the calcium content of the fruit.     

Stability of lipids and fatty acids in frozen and gamma irradiated Patagonian toothfish (Dissostichus eleginoides) from the Southwestern Atlantic

Patagonian toothfish were captured in the Southwestern Atlantic Ocean (FAO Zone N° 41). The fatty acid profile of total lipids and the triacylglycerol and phospholipid content of control and irradiated samples (1 and 5 kGy) stored at −18 °C were analyzed at 0 and 293 days post irradiation. The fatty acids are mainly monounsaturated acids (47 g/100 g total fatty acids), the most abundant one being oleic acid (18:1 n-9). This is followed in order of abundance by saturated fatty acids (26 g/100 g total fatty acids), consisting mainly of palmitic acid (16:0). Polyunsaturated fatty acids were less abundant (17 g/100 g total fatty acids) and consisted mainly of eicosapentaeonic (20:5 n-3) and docosahexaenoic (22:6 n-3) acids. Triacylglycerol content was 563.07 mg/mL oil, whereas phospholipids were 11.21 mg/mL oil. Gamma irradiation did not significantly affect the fatty acid profile or triacylglycerol and phospholipid content of P. toothfish stored for 293 days at −18 °C. The results suggest that the species exhibits a marked stability when subjected to irradiation and prolonged storage in the frozen state.     

Deodorisation process variables for croaker (M. furnieri) oil

Fish oil is the major food source of the long-chain omega-3 polyunsaturated fatty acids. Deodorisation represents a critical step of the refining process since it involves high temperature that could induce degradation reactions which affect oil integrity and quality. The present study evaluated the effect of the deodorisation variables (temperature, time and steam) on the croaker (Micropogonias furnieri) oil refining process. The evaluated parameters were Lovibond color (LC), free fatty acids (FFA), peroxide (PV), Iodine (IV) and Saponification (SV) values. The best deodorisation conditions were at 220 °C, 60 min and 5% of steam (based in oil mass), resulting in oil with LC of 0.4 red and 30 yellow, FFA of 0.09%, PV of 0.53 meq/kg. IV and SV were not significantly affected. The obtained fish oil presented high quality and oxidative stability, as well as EPA and DHA contents of approximately 12% of total fatty acids.     

The water vapour permeability,mechanical properties and solubility of fish gelatin–chitosan films modified with transglutaminase or 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and plasticized with glycerol

The effect of glycerol on the mechanical and water barrier properties, as well as on the water solubility, of fish gelatin–chitosan films (4:1, w/w) cross-linked with TGase or EDC was determined. The addition of glycerol in concentrations up to 30% (of the substrate mass) to the fish gelatin–chitosan films modified with TGase or EDC did not change their solubility in buffers of pH 3 and 6 at 25 °C or during heating at 100 °C for 60 min. The chemical and enzymatic cross-linking of the components did not increase the water barrier properties of the films. WVP of the films modified with EDC and TGase was not affected by glycerol at concentrations up to 25% of the substrate mass. Tensile strength of the films decreased after modification of the components with TGase or EDC, respectively, by about 25% and 40%. The elongations of the enzymatically modified films containing 20% of glycerol and of chemically modified films containing 15% of glycerol were, respectively, about 8 and 13 times higher than those of unplasticized films; however, the tensile strengths of plasticized films were, respectively, 2.5 and 5 times lower.     

Aldehyde formation in frozen mackerel (Scomber scombrus) in the presence and absence of instant green tea

The effect of frozen storage on lipid peroxidation in Atlantic mackerel (Scomber scombrus) stored for up to 26 weeks at −10 or −80 °C (control), with and without green tea antioxidants, was investigated. Hydroperoxides (PV) and aldehydes (TBARS) were measured by HPLC and LC–MS and hexanal by GC. There was an increase in peroxide value which was associated with an increase in aldehydes, followed by hexanal increase with storage time and at a higher temperature of −10 °C compared with samples stored at −80 °C. Although TBARS is a common assay used to follow malondialdehyde formation, other aldehyde products can also react with thiobarbituric acid to give the red chromogen. Analysis of aldehyde–TBA adducts by LC–MS confirmed the presence of malondialdehyde and, in particular, we report the production of gluteraldehyde for the first time in stored frozen fish. Green tea (at 250 ppm) substantially slowed down the oxidation process, whereas at 500 ppm it was less effective.     

Oxidative stability of fish oil supplemented with carnosic acid compared with synthetic antioxidants during long-term storage

The effects of carnosic acid (CA) of different concentrations (0.1, 0.2, and 0.3 mg/g) and synthetic antioxidants on oxidative stability in fish oil stored for 66 days at different temperatures (30 and 4 °C) were compared. The investigation focused on the increase in peroxide and conjugated diene values, as well as free fatty acid and thiobarbituric acid-reactive substances. The changes in trans fatty acid and aldehyde compound contents were investigated by Fourier transform infrared spectroscopy, while the changes in polyunsaturated fatty acid content were monitored by gas chromatography–mass spectrometry. The results show that the three CA concentrations were more effective in restraining fish oil oxidation, in which a dose–response relationship was observed. The antioxidant activity of CA was stronger than that of vitamin E, but still weaker than that of tertiary-butyl hydroquinone. Fish oil supplemented with 0.2 mg/g CA exhibited favourable antioxidant effects and is preferable for effectively avoiding oxidation.     

Evaluation of some physico-chemical properties of restructured trout and hake mince during cold gelation and chilled storage

Cold gelation was carried out on trout (Oncorhynchus mykiss) or on hake (Merluccius merluccius) mince with or without addition of fish oil and using microbial transglutaminase (MTGase). Products were stored at 4 °C for 6 days and lipid oxidation, protein oxidation, texture, water binding capacity, and colour were followed. Results indicated that MTGase was able to generate gels with good properties for both trout and hake. Gels prepared with trout were oxidised whilst gels prepared with hake were stable toward oxidation even in the presence of 5% fish oil. However, in the presence of oil, as an alternative for generating omega-3 enriched products, the activity of MTGase was impaired, as the gels took longer to reach maximum hardness. Furthermore, in all samples containing MTGase, protein oxidation was high.     

Lipid profiles of oil from trout (Oncorhynchus mykiss) heads,spines and viscera: Trout by-products as a possible source of omega-3 lipids?

Lipid profiles of fish oil extracted from trout heads, spines and viscera using supercritical carbon dioxide and Randall extraction with hexane were measured. The amount of unsaturated fatty acids (as a percentage of total fatty acids) was within the range of 72.6–75.3% in all the substrates. A significant presence of the most important omega-3 fatty acids was detected. Eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) content in oil from spines, heads and viscera resulted to be 8.7% and 7.3%, 7.9% and 6.3%, and 6.4% and 6.0%, respectively. A low (≈3%), but worth noting, presence of lipids with omega-1 polyunsaturated fatty chains was observed in all the oils. Finally, significant differences were noticed in the relative amounts of triacylglycerides (TAG), diacylglycerides (DAG) and free fatty acids (FFA). Whereas oil from heads and spines was essentially composed of TAG (≈98%), in viscera oil the molar distribution ratio became TAG:DAG:FFA = 87:8:5.     

Physiological responses and quality attributes of table grape fruit to chitosan preharvest spray and postharvest coating during storage

The effects of preharvest chitosan spray (PCS) or/and postharvest chitosan coating (PCC) treatments on the quality and physiological response of table grape fruit stored at 20 or 0 °C was evaluated, respectively. PCS/PCC treatment showed the best control effect on decay. PCC or PCS/PCC treatment significantly decreased the weight loss of fruit stored at 20 °C. Additionally, all chitosan treatments inhibited the increase in rate of soluble solid content to titratable acid in fruit, stored at 20 °C, while enhancing the rate at 0 °C and affecting the content of total phenolic compounds in the fruit. Furthermore, the activities of superoxide dismutase decreased in all chitosan treatments and PCS or/and PCC treatments also changed the activities of polyphenol oxidase, peroxidase and phenylalanine ammonia-lyase. The results indicated the beneficial effect of chitosan by preharvest spray and/or postharvest coating on fruit quality and resistance to fruit decay.     

Supercritical carbon dioxide extraction of polyunsaturated fatty acids from Northern shrimp (Pandalus borealis Kreyer) processing by-products

This study investigated the potential of Northern shrimp (Pandelus borealis Kreyer) by-products as a source of omega-3 polyunsaturated fatty acids (ω-3 PUFAs). The by-products (heads, shell and tail) of processing accounted for approximately 50–60% of the catch. Supercritical CO₂ extraction (SFE) of the by-products at 35 MPa and 40 °C generated a deep red oil, rich in ω-3 PUFAs, specifically 7.8 ± 0.06% eicosapentaenoic acid (EPA) and 8.0 ± 0.07 % docosahexaenoic acid (DHA).     

Combined effect of light salting,modified atmosphere packaging and oregano essential oil on the shelf-life of sea bream (Sparus aurata): Biochemical and sensory attributes

The combined effect of modified atmosphere packaging (MAP: 40% CO₂/30% O₂/30% N₂) and oregano essential oil, on the shelf-life of lightly salted cultured sea bream (Sparus aurata) fillets stored under refrigeration was studied. Quality assessment was based on sensory analysis and biochemical indices determination. Total volatile basic nitrogen (TVBN) and trimethylamine nitrogen (TMAN) values were higher in sea bream fillets stored in air followed by salted fillets stored in air. For salted sea bream fillets stored under MAP the inhibition in the TVBN and TMAN values was evident in the order MAP < MAP/0.4% (v/w) oregano oil < MAP/0.8% (v/w) oregano oil indicating the preservative effect of oregano oil. Salting had a noticeable preservative effect but produced an increase in the 2-thiobarbituric acid (TBA) values while oregano oil had a strong antioxidant activity giving the lowest TBA values. All raw sea bream fillet samples received acceptable sensory scores during the first 15–16 days of storage. The salted samples remained acceptable up to ca. 20–21 days while the MAP salted samples up to ca. 27–28 days of storage. The oregano oil addition in MAP salted samples yielded a distinct but pleasant flavor and contributed to a considerable slower process of fish spoilage given that the fillets treated with 0.8% (v/w) oregano oil were still sensory acceptable after 33 days of storage. The preservative effect was greater as the oregano oil concentration was greater.