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effeective storage of copia
1. Effects of packaging methods and temperature
on the lipid quality changes of Cobia (Rachycentron
canadum) fillets during frozen storage
Thi Hang Nguyen,
Faculty of Food Science and Nutrition, University
of Iceland, hangnt@ntu.edu.vn
2. Introduction
• Cobia fillets contain:
Lipid content: 5.3-16.6%
MUFA: 34%
PUFA: 15.5%
Cobia lipids may be susceptible to lipid
oxidation during processing and storage
Objectives
Evaluate effects of air packaging and vacuum
packaging on the quality of cobia fillets during
frozen storage for 5 months.
Investigate effects of different storage
temperatures (-18 oC and -25 oC) on the quality
of cobia fillets during frozen storage for 5
months.
3. Fig. 1: Flow chart of the
experimental design
Raw materials and methods
Four experimental groups
1. Cobia fillets air packaged and stored at -18 oC (AP, -18 oC)
2. Cobia fillets air packaged and stored at -25 oC (AP, -25 oC)
3. Cobia fillets vacuum packaged and stored at -18 oC (VP, -18 oC)
4. Cobia fillets vacuum packaged and stored at -25 oC (VP, -25 oC).
Analyses
Water and total lipid (TL) content
Phospholipid (PL) content
Free fatty acids (FFA)
Lipid hydroperoxides (peroxide value, PV)
Thiobarbituric acid reactive substance (TBARS)
Sampling time: every month up to 5 months of storage
4. Results and Discussion
60
63
66
69
72
75
0 1 2 3 4 5
Watercontent(%)
Storage time (months)
(A)
Fig. 2: Water content (%) (A) and total lipid content (%) (B) in vacuum packaged (VP) and air packaged
(AP) frozen cobia fillets during 5 months frozen storage at -18 oC and -25 oC.
0
3
6
9
12
15
0 1 2 3 4 5
Totallipidcontent(%)
Storage time (months)
(B)
5. Fig. 3: PL content (A) and Free fatty acid (g FFA/100 g TL) (B) in vacuum packaged (VP) and air packaged
(AP) frozen cobia fillets during 5 months frozen storage at -18 oC and -25 oC.
0
1
2
3
0 1 2 3 4 5
Phospholipid(%ofTotallipid)
Storage time (months)
0
1
2
3
4
5
0 1 2 3 4 5
gFFA/100glipid
Storage time (months)
(B)(A)
Results and Discussion
6. Fig. 4: Lipid hydroperoxide (PV; mol/kg muscle) (A) and thiobarbituric acid reactive substance (TBARS; mol
MDA/kg muscle) content (B) in vacuum packaged (VP) and air packaged (AP) frozen cobia fillets during 5 months
frozen storage at -18 oC and -25 oC.
0
20
40
60
80
100
0 1 2 3 4 5
Lipidhydroperoxide
(µmol/kgmuscle)
Storage time (months)
(a)
0
5
10
15
20
25
30
0 1 2 3 4 5
TBARS(µmol/kgmuscle)
Storage time (months)
(A) (B)
Results and Discussion
7. Conclusions
• The farmed cobia was a fatty fish species with 70.9 ± 1.2% moisture and 10.1 ± 0.2% lipid
content
• Several lipid quality changes occurred in all samples during the frozen storage
• The storage time showed the strong effect on lipid hydrolysis and oxidation all frozen cobia
fillets.
• Vacuum packaging significantly reduced lipid oxidation compared to air packaging
• A lower storage temperature had some effective retardations in lipid degradation
• It can be suggested that vacuum packaging in combination with a storage temperature of -18
oC or lower can be applied to remain product stability
As you know: fish is one of important food sources for human consumption, because it contains high quality protein and unsaturated fatty acids, especially EPA and DHA.
However, fish is perishable.
Freezing and subsequent frozen storage are applied widely to maintain fish quality.
During frozen storage, although bacterial activity is inhibited, fish quality is still degraded. The most important deterioration is lipid oxidation.
So, the objectives are to …
After harvesting, fish was processed as frozen fillets products. After freezing, a half of samples was individually air parkaged, the rest fillets was individually vacuum packaged . The products were then stored at different temperature. SO, we had 4 experimental groups like in slide.
Generally, water was stable during storage for 5 months, except for air packaged samples at -25. The temperature had no effect on water content. After 4 month, vacuum packaged samples had higher water content than air packaged samples.
PL is one of lipid group locating in the membrance of cells. PL decreased significantly during storage time for 5 months show PL was broken down due to phospholipase enzyme. No influence of temperature and packaging method on PL degradation. On the other hand, there was a major increase in FFA, especiall in the first three months of storage. As you know FFA formation from lipid and PL hydrolysis by enzyme activity. The decrease in FFA may be due to the further oxidation of FFA. PM did not show any effect in FFA generation. However, a lower temperature showed effectively inhibition in FFA formation.
PV increased in all groups, and the increase in PV was more pronounced in air packaging samples. Vacuum packaging method effectively inhibited lipid oxidation, more clear from month 3.
The storage time had a strong effect on lipid deterioration in frozen cobia fillets
VP significantly delayed lipid oxidation
A lower storage temperature could reduce lipid changes