Cholesterol and lipid oxidation in raw and pan‐fried minced beef stored under aerobic packaging

BACKGROUND: The type of packaging atmosphere has been reported as a technological factor that consistently affects the quality of lipid fraction in meat. Oxidation of cholesterol and lipids was evaluated before and after pan frying in commercial refrigerated minced beef stored under aerobic atmosphere for 1 and 8 days. RESULTS: In raw beef, cholesterol and lipid oxidation developed at a slow rate. Cholesterol oxidation products (COPs) did not significantly vary (～8 µg COPs g^?1 of fat) over 8 days, while in the same period thiobarbituric acid reactive substances (TBARS) less than doubled (from 0.7 to 1.2 malondialdehyde equivalents kg^?1 of muscle). Pan frying did not influence the oxidative degree in the fresh product but consistently catalyzed cholesterol oxidation in stored beef. A significant increase was assessed in beef at the end of storage: from 8.6 to 30.0 µg COPs g^?1 of fat in raw and cooked beef, respectively. CONCLUSION: Aerobic packaging did not appear as a pro‐oxidant factor in fresh minced beef with a good oxidative quality during a short period of refrigerated storage. Copyright © 2010 Society of Chemical Industry     

Cholesterol oxidation products in irradiated raw meat with different packaging and storage time

The effect of irradiation and packaging conditions on the formation of cholesterol oxidation products (COPs) as well as lipid oxidation products was determined in raw turkey leg, beef, and pork loin meat during 7 days of storage. Ground turkey leg, beef, and pork loin muscles were prepared as patties. The patties were individually packaged either in oxygen-permeable or impermeable bags, irradiated at 0 or 4.5 kGy using a Linear Accelerator, and stored at 4°C. The COPs such as 7-hydroxycholesterol, 7β-hydroxycholesterol, and 7-ketocholesterol were detected in fresh raw meats at 0 day at the level of 10.9 to 49.2 μg/g lipid. After 7 days of storage, other COPs such as epoxides, 20-hyroxycholesterol, and choletanetriol were formed in mainly aerobically packaged and irradiated raw meats. Packaging effect was more crucial on the cholesterol and lipid oxidation than irradiation. In aerobically packaged and irradiated meats, turkey leg muscles had higher COPs value than beef or pork did. COPs and thiobarbituric acid reactive substances (TBARS) values had a strongly positive correlation in turkey leg and pork. But, cholesterol oxidation in beef proceeded in irradiated and aerobically stored samples despite of its low level of TBARS value.     

Cholesterol photosensitised oxidation of beef meat under standard and modified atmosphere at retail conditions

The effect of the fluorescent light exposure and type of packaging (normal atmosphere and oxygen-rich atmosphere) was evaluated on the oxidation parameters (peroxides and cholesterol oxidation products) of raw beef slices placed in packed vessels and refrigerated. The concentration of COPs in meat treated under modified atmosphere ranged from 0.15 to 0.52mg/100g meat (average value of 0.27mg COPs/100g meat), which was twice as much as the average COPs content (0.14mg/100g) of meat packed under air (0.04-0.27mg COPs/100g meat). The main cholesterol oxide was 7k, which represented about one third of the total cholesterol oxides, followed by 7β-OH (20-25% of total COPs), 7α-OH (about 20%) and β-epoxy (12-18%). In normal atmosphere, photoxidation was a superficial process, since an inverse correlation between meat slice weight and COPs content on a lipid basis was observed, unlike in a high oxygen (32%) atmosphere.     

Effect of irradiation and packaging conditions after cooking on the formation of cholesterol and lipid oxidation products in meats during storage

The effect of irradiation and packaging conditions on the content of cholesterol oxidation products (COPs) and lipid oxidation in cooked turkey, beef, and pork during storage was studied. Ground turkey leg, beef, and pork were cooked, packaged either in oxygen-permeable or oxygen-impermeable bags, and irradiated at 0 or 4.5 kGy. Lipid oxidation and COPs were determined after 0 and 7 days of storage at 4°C. Packaging of cooked meat was more important than irradiation in developing COPs and lipid oxidation in cooked meats during storage. 7-Hydroxycholesterol, 7β-hydroxycholesterol, β-epoxide, and 7-ketocholesterol were among the major COPs formed in cooked turkey, beef, and pork after storage, and their amounts increased dramatically during the 7-day storage in aerobic conditions. Irradiation had no significant effect on the amounts of any of the COPs found in cooked turkey and beef, but increased (P<0.05) the amounts of - plus 7β-hydroxycholesterol, β-epoxide, 7-ketocholesterol, and total COPs in aerobically packaged cooked pork. The amounts of COPs and lipid oxidation products (TBARS) closely related to the proportion of polyunsaturated fatty acids in meat. The results indicated that the composition of fats in meat is important on the oxidation rates of lipids and cholesterol, and packaging is far more important than irradiation in the formation of COPs and lipid oxidation in cooked meat.     

Cholesterol and Lipid Oxidation Products in Cooked Meat as Affected by Raw-Meat Packaging and Irradiation and by Cooked-Meat Packaging and Storage Time

Aerobic packaging significantly increased cholesterol oxidation products (COPs) and thiobarbituric acid reactive substances (TBARS) in cooked turkey, pork, and beef patties after 7‐d storage, but vacuum packaging was very effective in preventing cholesterol and lipid oxidation. Packaging of meat after cooking had a much stronger effect on COPs formation than before cooking, and irradiation had only a minor effect. The amount of total COPs correlated well with TBARS in cooked meat. Turkey had the highest rates of COPs and TBARS formation and beef had the lowest rates after 7‐d storage, which were closely related to the fatty acid composition of meats. 7a‐hydroxycholesterol, 7p‐hydroxycholesterol, and 7‐ketocholesterol were the major COPs detected in all 3 cooked meat patties.     

Lipid and cholesterol oxidation in Chinese-style sausage using vacuum and modified atmosphere packaging

The oxidation of lipid and cholesterol in Chinese-style sausage in vacuum packaging (VP) and modified atmosphere packaging (MAP) stored at 4°C and 15°C, respectively, for 5 months was investigated. The 2-thiobarbitaric acid reactive substance (TBARS) and peroxide value (POV) of sausage were variable with packaging treatments during storage. TBARS and POV in sausage stored at 15°C were significantly greater (p < 0·05) than at 4°C, and the MAP treatment was more stable than the VP treatment. In addition, the polyunsaturated fatty acids (PUFA) in sausage decreased with storage for both treatments. The content of cholesterol decreased significantly after 3 months of storage. 7-β-hydroxycholesterol, 7-ketocholesterol and 22-ketocholesterol were the major cholesterol oxidation products (COPs), but there was no detectable (< 1 μg/100 g) 25-hydroxycholesterol or cholestanetriol with either treatment.     

Addition of tea catechins and vitamin C on sensory evaluation, colour and lipid stability during chilled storage in cooked or raw beef and chicken patties

The effects of addition of tea catechins (TC) and vitamin C (VC) on sensory evaluation, colour and lipid stability in cooked or raw beef and chicken meat patties during refrigerated storage were studied. Fresh beef striploin and chicken breast muscles were minced, following removal of external fat and connective tissue. Following mincing, beef and chicken were assigned to one of the following five treatments: control (meat treated with no antioxidant); TC200, meat plus 200 mg TC/kg muscle; TC400, meat plus 400 mg TC/kg muscle; VC200, meat plus 200 mg VC/kg muscle, VC400, meat plus 400 mg VC/kg muscle. Sodium chloride (1%) was added to all samples. Patties (125 g portions), formed from the above-treated minced meat, were oven cooked, cooled, and packaged in 30% CO₂:70% N₂. Fresh raw beef and chicken patties were packaged in 80% O₂:20% CO₂. All samples were stored for up to 7 days under fluorescent lighting at 4 °C. Sensory parameters (colour, flavour, taste, tenderness and overall acceptability) were evaluated on cooked beef and chicken patties after 1, 3 and 6 days of storage. Surface colour (Hunter L, a and b values), and lipid oxidation (2-thiobarbituric acid reactive substances) were measured on days 1, 3 and 6 of storage for cooked meats and on days 2 and 7 for raw beef and chicken. Tea catechins addition (200 or 400 mg/kg) to minced meat caused (P < 0.05) discolouration in cooked beef and chicken meat patties and significantly reduced (P < 0.001) lipid oxidation in cooked or raw beef patties compared to the control. Beef, either raw or cooked, was more susceptible (P < 0.01) to oxidation compared to chicken. Raw meat stored in high oxygen conditions was more susceptible to lipid oxidation than cooked meat stored in anaerobic conditions. Tea catechins treatments (TC200 and TC400) inhibited (P < 0.05) lipid oxidation in raw beef to a greater extent than vitamin C treatments (VC200 and VC400). These results indicate that tea catechins are potent natural antioxidants and exhibit greater antioxidant efficacy compared to vitamin C.     

The combined effect of antioxidants and modified atmosphere packaging on protein and lipid oxidation in beef patties during chill storage

Effect of rosemary extract and ascorbate/citrate (1:1) in combination with modified atmosphere packaging (100% N(2), 80% O(2)/20% N(2)) on protein and lipid oxidation in minced beef patties during storage in the dark for up to 6 days at 4°C was investigated. A high level of oxygen in the packaging atmosphere was found to increase both lipid and protein oxidation during storage as evaluated by TBARS analysis of secondary lipid oxidation products and by 2,4-dinitrophenylhydrazine derivatization of protein carbonyls. Both antioxidant systems tested were found to inhibit lipid oxidation but not protein oxidation. In contrast, ascorbate/citrate was found to promote protein oxidation. Rosemary extract was found to regenerate or protect α-tocopherol whereas the packaging atmospheres had no effect on α-tocopherol stability. In high oxygen atmospheres both antioxidants protected the fresh red meat colour with ascorbate/citrate being more efficient than the rosemary extract, whereas no effect of antioxidant on meat colour was found in beef patties stored in 100% nitrogen.     

Cholesterol photosensitised oxidation of horse meat slices stored under different packaging films

The effect of the type of packaging film (transparent vs. light-protecting red film) was evaluated on the formation of cholesterol oxidation products (COPs) in refrigerated horse meat slices stored in retail conditions under light exposure for 8 h. In meat wrapped with a transparent film, COPs increased from 233 (control) to 317 μg/g of fat, whereas the red film delayed cholesterol oxidation and offered protection against COPs formation, since COPs decreased from 173 (control) to 139 μg/g of fat after 8 h of light exposure. In addition, light opened the epoxy ring and led to the formation of triol, which was actually absent at T_0. A proper packaging film may represent a useful strategy to retard oxidative degradation in a light-sensitive, high pigment- and fat-containing food, such as horse meat.     

Antioxidative/Antimicrobial effects of galangal and alpha-tocopherol in minced beef

The antioxidant and microbial stabilities of galangal (Alpinia galanga) extract in raw minced beef were examined at 4 +/- 1 degree C. Raw minced beef containing galangal extracts (0 to 0.10%, wt/wt) were prepared. Lipid oxidation during refrigerated storage was assessed by monitoring malonaldehyde formation, using the thiobarbituric acid reactive substances method. In minced beef, added galangal extract improved oxidative stability. Galangal extract at higher concentrations of 0.05% and 0.10% (wt/wt) were also found to extend the shelf-life of minced beef. Addition of alpha-tocopherol (0.02%, wt/wt) to galangal extract (0.05%, wt/wt) were observed to increase the oxidative but not the microbial stability of minced beef during the storage of 7 days. Galangal extract may prove useful in inhibiting lipid oxidation and increasing microbial stability of minced meat.     

乳酸钙对牛肉糜色泽稳定性的影响

为研究乳酸钙对牛肉糜色泽稳定性的影响,将牛背最长肌绞碎成肉糜,分别添加0.1%、0.3%、0.5%的乳酸钙溶液,研究在(4±1)℃的冷藏条件下,肉糜肉色稳定性、色素含量、脂肪氧化及高铁肌红蛋白还原酶活性随时间的变化。结果表明：在7d的贮藏期内,添加不同质量分数乳酸钙均可有效抑制高铁肌红蛋白的生成和脂肪氧化的发生,并显著提高高铁肌红蛋白还原酶活性和肉色稳定性,但会使肉糜L*值显著降低(P＜0.05)。其中0.3%的乳酸钙对稳定肉色有显著作用,护色效果明显。     

Effect of dietary α-tocopherol supplementation and gamma-irradiation on α-tocopherol retention and lipid oxidation in cooked minced chicken

The effects of dietary α-tocopherol supplementation and gamma-irradiation on α-tocopherol retention and lipid oxidation in cooked minced chicken during refrigerated storage were studied. Minced breast and thigh meat from broilers fed diets supplemented with 100, 200 or 400 mg α-tocopheryl acetate/kg feed was irradiated at 2.5 or 4.0kGy. Cooked irradiated and unirradiated meat was stored at 4 °C for 5 days. α-Tocopherol concentrations increased with increasing dietary supplementation. Concentrations decreased during storage, but retention was not affected by irradiation. Lipid stability was determined by measuring the formation of thiobarbituric acid-reacting substances (TBARS) and cholesterol oxidation products (COPs) during storage. TBARS and COPs increased during storage and were reduced by increasing levels of dietary α-tocopheryl acetate supplementation. Irradiation accelerated TBARS formation during storage, but this was prevented by supplementation with 200 mg α-tocopheryl acetate/kg feed. Irradiation tended to increase COPs during storage, although no consistent effects were observed. In general supplementation with over 400 mg α-tocopheryl acetate/kg feed may be required to control cholesterol oxidation in minced chicken. The results suggest that, overall, irradiation had little effect on lipid stability in α-tocopherol-supplemented meat following cooking and storage.     

喷雾冷冻干燥对葛仙米藻胆蛋白抗氧化特性的影响

研究喷雾冷冻干燥对葛仙米藻胆蛋白抗氧化特性的影响,并与冷冻干燥技术进行比较。主要测定ABTS+ ·、铁还原抗氧化能力(FRAP)、对羟自由基( ·OH)清除作用和H2O2诱导的脂质过氧化的抑制作用,结果发现,喷雾冷冻干燥(SFD)对葛仙米藻胆蛋白的抗氧化特性有一定的影响,在基于电子转移和氢原子转移的抗氧化测定方法中,SFD与冷冻干燥(FD)制备的样品差异不明显,但在基于活性氧自由基清除的测定方法中,SFD显著优于FD。表明SFD非常适合于高活性成分的干燥。     

Effect of Fe2+, Salt, Cooking and Shredded CoffiR on Thiobarbituric Acid (TBA) Numbers in Ground Beef

Presence of ferrous iron (Fe²⁺) and/or salt (NaCl) in ground beef followed by cooking and storage resulted in marked increases in lipid oxidation as measured by TBA values. Addition of an edible collagen film (Coffi^R) to minced fresh beef did not influence TBA values. Cooking fresh ground beef resulted in lowering of TBA values (when compared to raw beef), but TBA values increased more rapidly and to a greater extent in cooked beef than in raw samples during 7 days refrigerated storage.     

Combined effect of cooking (grilling and roasting) and chilling storage (with and without air) on lipid and cholesterol oxidation in chicken breast

The oxidation of the lipid fraction and cholesterol in raw and cooked chicken breast samples stored for 0 and 6 days at 4 degrees C under aerobic conditions and in vacuum packaging was studied. The multivariate statistical analysis showed significant effects of both culinary process and storage conditions on the lipid and cholesterol oxidation process, with a significant interaction between the two variables. Aerobic storage increased thiobarbituric acid reactive substances (TBA) from 0.04 to 0.06 ppm for raw samples, from 0.21 to 1.20 ppm for grilled samples, and from 0.24 to 1.62 ppm for roasted samples. During vacuum storage, only roasted samples showed significant increases in TBA. Levels of total cholesterol oxidation products (COP) remained low (2.88 to 4.35 microg/g of lipid) for all raw samples. Cooking increased COP levels to 12.85 and 11.54 microg/ g of lipid for grilled and roasted samples, respectively. Total COP and all individual COP except for cholestanetriol were significantly correlated with TBA and the peroxide index. However, the most extensive effect was attributable to the aerobic storage of cooked samples, which led to COP levels of 92.35 and 88.60 microg/g of lipid in grilled and roasted samples, respectively. Vacuum packaging did not increase COP levels for cooked samples.     

Effect of dietary vitamin E supplementation, fat level and packaging on colour stability and lipid oxidation in minced beef

The effect of addition of vitamin E (2025 IU animal(-1) day(-1)) to the diet of beef bulls on the colour stability and lipid oxidation of minced beef was studied. Control and enriched diets were provided for the last 136 days before slaughter. Batches of freshly minced meat were prepared containing approximately 1.3 and 22.2 wt% fat, respectively. Half of the samples of minced meat from control (CON) and supplemented (SUP) beef were packaged on trays with oxygen-permeable over wraps and half in modified atmosphere (MA) packs (initial gas mixture: O(2)/CO(2)/N(2)=65/25/10). The minced beef was stored for 10 days at 7°C in an illuminated environment. The SUP meat at both fat levels was consistently more resistant to lipid oxidation than was the CON meat. The additional vitamin E had a greater anti-oxidant effect for the lean meat product. MA packaging in comparison to the oxygen-permeable foil over-wrap did increase lipid oxidation, the effect being most pronounced for the CON meat. A sensory panel considered the colour of the lean SUP meat during display as more attractive than that of lean CON meat, irrespective of packaging. A similar effect was observed occasionally for the relatively fat minced meat. These subjective findings were confirmed by objective assessment of colour. The stability of the colour of the MA packed meat was better than that of the oxygen-permeable foil-wrapped meat. Microbial growth patterns of enriched and control meat were similar. MA packaging retards the multiplication of mesophilic aerobic spoilage micro-organisms and Enterobacteriaceae.     

Effects of dietary vitamin e supplementation and packaging on the quality of minced beef

Friesian cattle, aged 26-27 months, were fed a diet supplemented with 2000IU α-tocopheryl acetate/kg feed/day and another group was fed a basal diet (20IU/kg feed/day) for approximately 50 days prior to slaughter. Following frozen storage (-20°C for 8 weeks) semimembranosus muscles from basal and α-tocopheryl acetate supplemented cattle were minced and vacuum packaged, aerobically packaged or packaged under modified atmospheres (MAP) (30% O(2): 70% CO(2); 70% O(2): 30% CO(2); 80% O(2): 20% CO(2)). Samples were held under refrigerated (4°C) display (fluorescent lighting, 616 lux) for eight days. Vacuum-packaged samples were held under similar conditions but in complete darkness and allowed to bloom for a minimum of 4hr prior to taking colour readings. TBARS values and Hunter a values in minced beef were measured every two days. α-Tocopherol concentrations were significantly (p<0·05) higher in minced meat samples from the supplemented group than in the basal group. Significant (p<0·05) reductions in α-tocopherol concentrations in supplemented meat samples were observed with increased concentrations of oxygen in different packaging systems after eight days of refrigerated storage. TBARS values were reduced over the whole retail display period for all packaging systems when α-tocopheryl acetate supplemented beef was used. TBARS values increased as oxygen levels increased in MAP. Hunter a values showed that vitamin E supplementation in combination with vacuum packaging and MAP improved the colour stability of meat during the first 4 days of storage, however, the failure of MAP to extend meat colour for longer periods of time was probably the result of prior storage at -20°C for 8 weeks.     

Lipid and colour stability of beef from grazing heifers supplemented with sunflower oil alone or with fish oil

The effect of sunflower and fish oil supplementation of grazing heifers on lipid oxidation and colour stability in beef was investigated. For 150 days, heifers were assigned unsupplemented grazing (G) or restricted grazing with 2.5 kg concentrates containing 1250 I.U. -tocopheryl acetate and 290 g sunflower oil (S1), 415 g sunflower oil (S2), 290 g sunflower + 85 g fish oil (FS1) or 415 g sunflower + 85 g fish oil (FS2). Longissimus dorsi muscle was excised 24 h post-mortem and stored at −30 °C prior to analysis. Muscle -tocopherol in the oil-supplemented groups was higher (P < 0.05) than the G group. Lipid oxidation in refrigerated, minced raw or cooked beef was not significantly affected by diet but metmyoglobin was higher (P < 0.05) in raw beef from oil-supplemented groups compared to the G group. Lipid oxidation and metmyoglobin formation increased (P < 0.001) during refrigerated storage. Vitamin E supplementation together with pasture grazing appeared to offset any potential deleterious effect of oil supplementation on lipid and colour stability.     

Determination of cholesterol oxidation products in raw and processed beef and pork preparations

The effect of pan-frying on the formation of cholesterol oxidation products (COPs) in different processed meat samples (beef patties, braised meat, and fillets of pork) was studied. Samples were pan-fried with or without addition of oil. Different unsaturated oils (olive oil, corn oil or partly hydrogenated plant oil) were used throughout the study. After extraction, seven toxicologically relevant COPs were analyzed using LC–MS. Prior to heat processing up to 6.7 mg COPs/kg extracted fat could be detected in the raw material. Neither the cholestanetriol nor 25-hydroxycholesterol, which are the most cytotoxic COPs in vitro, were detectable in any sample. Differences in the COPs contents were observed between beef (up to 16.5 mg/kg extracted fat) and pork (up to 22.2 mg/kg extracted fat) samples. In prepared samples higher COPs content was noted compared with raw samples. Generally, a certain order of COPs increase dependent on the plant oil used could be recognized: corn oil < partially hydrogenated plant oil < olive oil. It appears that short heating time, mild heating conditions, and the use of fresh and shortly stored raw materials keep COPs levels low.     

Use of microwave in chicken breast and application of different storage conditions: consequences on oxidation

Slices of chicken breast were subjected to microwave heating (750 W, 3 min) and further storage in different conditions (refrigeration at 4 °C and freezing at −18 °C combined with aerobic, vacuum, and modified atmosphere packaging). Evaluation of the intensity of the oxidation process was carried out. A 16-fold increment in the amount of cholesterol oxidation products (COP) was found as a consequence of microwave cooking (45.86 μg/g lipid after microwave and 2.88 μg/g lipid in raw samples). 7-ketocholesterol was the most affected COP by microwave, accounting for a 25% of the total COP. Storage of microwaved samples under aerobic refrigeration led to the highest oxidation status with the following values: peroxide 19.41 meqO₂/kg lipid, TBA 0.32 ppm and COP 123.50 μg/g lipid. MAP refrigerated samples showed 50.94 μg/g lipid of total COP, an amount slightly higher than in vacuum conditions (46.81 μg/g lipid). Under frozen storage MAP and vacuum samples showed the lowest amounts of total COP (29.76 and 39.28 μg/g lipid, respectively).