Process engineering parameters and type of n-octenylsuccinate-derivatised starch affect oxidative stability of microencapsulated long chain polyunsaturated fatty acids

Aim of the present study was to investigate the impact of the emulsifying carrier matrix constituent, n-octenylsuccinate-derivatised (OSA)-starch, and process conditions on physical characteristics and oxidative stability of microencapsulated fish oil. Furthermore, the effect of the drying medium, i.e. air or nitrogen, on lipid oxidation during spray-drying and subsequent storage was investigated. Particle characteristics and lipid oxidation of microencapsulated fish oil were both influenced by the type of OSA-starch and the drying conditions. The highest oxidative stability was observed for fish oil microencapsulated in OSA-starch with the lowest average molecular weight and glucose syrup spray-dried at a moderate temperature setting. Particle characteristics of the microcapsules were not attributable for differences in lipid oxidation during storage. In spray-dried carrier matrix particles, the particle size increased with increasing average molecular weight of the OSA-starch and was attributed to an increase in air inclusion. Thus differences in lipid oxidation of the microencapsulated fish oil were attributed to differences in air inclusion as affected by the type of OSA-starch. In terms of spray-drying under inert conditions and in the presence of air, lipid oxidation of microencapsulated fish oil was rather attributed to oxygen availability in the feed emulsion than in the drying gas.     

Maillard Reaction Products as Encapsulants for Fish Oil Powders

The use of Maillard reaction products for encapsulation of fish oil was investigated. Fish oil was emulsified with heated aqueous mixtures comprising a protein source (Na caseinate, whey protein isolate, soy protein isolate, or skim milk powder) and carbohydrates (glucose, dried glucose syrup, oligosaccharide) and spray‐dried for the production of 50% oil powders. The extent of the Maillard reaction was monitored using L*, a*, b* values and absorbance at 465 nm. Encapsulation efficiency was gauged by measurement of solvent‐extractable fat and the oxidative stability of the fish oil powder, which was determined by assessment of headspace propanal after storage of powders at 35 °C for 4 wk. Increasing the heat treatment (60 °C to 100 °C for 30 to 90 min) of sodium caseinate‐glucose‐glucose syrup mixtures increased Maillard browning but did not change their encapsulation efficiency. The encapsulation efficiency of all heated sodium caseinate‐glucose‐glucose syrup mixtures was high, as indicated by the low solvent‐extractable fat in powder (<2% powder, w/w). However, increasing the severity of the heat treatment of the sodium caseinate‐glucose‐glucose syrup mixtures reduced the susceptibility of the fish oil powder to oxidation. The increased protection afforded to fish oil in powders by increasing the temperature‐time treatment of protein‐carbohydrate mixtures before emulsification and drying was observed irrespective of the protein (sodium caseinate, whey protein isolate, soy protein isolate, or skim milk powder) and carbohydrate (glucose, glucose/dried glucose syrup, or oligosaccharide/dried glucose syrup) sources used in the formulation. Maillard reaction products produced by heat treatment of aqueous protein‐carbohydrate mixtures were effective for protecting microencapsulated fish oil and other oils (evening primrose oil, milk fat) from oxidation.     

原生态与人工添加二十二碳六烯酸羊乳制品贮藏期脂肪酸稳定性比较

通过饲喂奶山羊富含二十二碳六烯酸（docosahexaenoic acid，DHA）的微藻粉，获得原生态DHA羊乳（DHA含量为30 mg/100 g原料乳），然后将其制作成超高温瞬时灭菌（ultra-high temperature instantaneous sterilization，UHT）乳及全脂乳粉，同时设立人工添加富含DHA微胶囊粉的UHT乳及全脂乳粉作为对照组，在常温（25 ℃）和高温（37 ℃）下进行为期28 d的贮藏实验，研究原生态与人工添加DHA羊乳制品贮藏期脂肪酸稳定性。结果表明，与人工添加组相比，贮藏期间原生态UHT乳及全脂乳粉的DHA含量下降速率明显减缓，在UHT乳中，人工添加组乳制品DHA含量降低率在37 ℃下最高达（40.92±3.52）%（贮藏第28天），此时原生态组DHA降低率为（36.70±4.84）%。贮藏期间，原生态与人工添加DHA的UHT乳及全脂乳粉中多不饱和脂肪酸相对含量总体均下降，且与人工添加DHA的乳制品相比，原生态组中多不饱和脂肪酸相对含量更高，更易氧化生成碳链更短的脂肪酸。此外，随着贮藏期的延长，原生态DHA乳制品组中的油脂氧化指标过氧化值和酸价上升速率明显低于人工添加DHA乳制品组。综上，本实验可为制备富含DHA的天然奶制品提供理论参考。     

Oxidative Stability of ω3-rich Camelina Oil and Camelina Oil-based Spread Compared with Plant and Fish Oils and Sunflower Spread

ABSTRACT: The oxidative stability of ω3‐rich oil from Camelina sativa and the storage stability of a camelina oil‐based spread were evaluated. Camelina oil was more stable than fish oil and linseed oil, but less stable than sunflower, corn, sesame, and olive oils, indicated by measuring peroxide values (PV), ρ‐anisidine values (AV), total oxidation values (Totox), thiobarbituric acid reactive substances (TBARS), conjugated diene levels (CD), and conjugated triene levels (CT) during storage at 65 °C for 16 d. The camelina oil‐based spread had higher PV, AV, Totox, TBARS, CD, and CT than the sunflower spread but maintained adequate sensory quality for 16 wk of storage at 4 °C or 8 °C.     

Enrichment of Chicken Nuggets with Microencapsulated Omega-3 Fish Oil: Effect of Frozen Storage Time on Oxidative Stability and Sensory Quality

This work studies for the first time the elaboration of frozen chicken nuggets enriched with microcapsules of omega-3 fatty acids using fish oil. Three types of chicken nuggets were prepared: control (C), enriched in bulk fish oil (BFO), and with added microencapsulated fish oil (MFO). Effect of length of frozen storage after pre-frying and before domestic frying was studied. The pre-fried nuggets were stored during 24 h at refrigeration temperature (0–2 °C) (T0) or during 1 month (T1M) or 3 months (T3M) in a domestic freezer at ?18 °C before frying. Length of frozen storage after pre-frying and before domestic frying promoted lipid and protein oxidative reactions in omega-3-enriched nuggets. Microencapsulation showed a protective effect against lipid and protein oxidation, especially during the first month of storage. In MFO, sensory traits were not affected by enrichment. In BFO-T0, a higher juiciness and saltiness and a less intense meat flavor in comparison with C-T0 and MFO-T0 was found. Time of frozen storage did not influence the sensory quality of chicken nuggets enriched with omega-3. Microencapsulation seems to be a promising method for enrichment of pre-fried frozen meat products with fish oil, improving the oxidative shelf life and preserving the sensory quality characteristics of the enriched products.     

Oxidative stability of ultra high temperature milk enriched in conjugated linoleic acid and trans-vaccenic acid

Milk naturally enriched in conjugated linoleic acid (CLA) and trans-vaccenic acid (TVA) was ultra high temperature (UHT)-treated at 125–145 °C for 2–20 s and stored at 4 and 25 °C for up to 120 d. The oxidative stability of treated enriched milk was evaluated in terms of changes on the contents of CLA and TVA, dissolved oxygen, hydroperoxides, thiobarbituric acid reactive substance (TBARS) and formation of volatiles. After UHT treatment, more than 78% of CLA and 87% of TVA remained. After 15 d of storage at 25 °C, the CLA and TVA were relatively stable with values in the range of 67–75 and 63–73%, respectively. During storage, CLA oxidized faster than TVA, independently of the UHT treatment and storage conditions. Heptanal was the most abundant volatile resulting from UHT processing and a potential suitable marker for heat treatment of milk rich in CLA and TVA.     

Lipolysis and Oxidation in Ultra‐High Temperature Milk Depend on Sampling Month,Storage Duration,and Temperature

During storage, some factors (for example, storage duration and temperature) can affect milk stability and consumer acceptability. Thiobarbituric acid reactive substances (TBARSs), lipid classes, and fatty acid profiles in stored ultra‐high temperature (UHT) milk were analyzed to assess the effects of storage time and temperature on lipid oxidation and lipolysis. With storage duration up to 12 months, the milk fat phase was separated and showed high levels of oxidation and lipolysis, manifested as increased levels of TBARS and free fatty acids. High oxidation levels decreased the percentage of unsaturated fatty acids (UFAs) in triacylglycerol and phospholipids. Higher storage temperatures (20, 30, and 37 °C) resulted in a higher degree of fat aggregation, oxidation, and lipolysis compared with refrigerated storage (4 °C). Additionally, sampling month of raw milk (May, July, and November) affected the lipid profiles of UHT milk during storage, with more UFA oxidized in July than in the other 2 months.     

Iron-Lactoferrin Complex Reduces Iron-Catalyzed Off-flavor Formation in Powdered Milk with Added Fish Oil

Abstract: The iron–lactoferrin complex (FeLf) is useful for dietary iron supplementation. However, the effects of FeLf on iron‐catalyzed off‐flavors in lipid‐containing food products have not been reported. In this study, we investigated the effects of FeLf on off‐flavors development during the production and storage of powdered milk with added fish oil. Powdered milk samples were formulated with FeLf or iron (II) sulfate, then stored at 37 °C for 5 mo. A sensory evaluation revealed that FeLf delayed the development of oxidized flavor and reduced metallic taste in the powdered milk compared with iron (II) sulfate. Headspace gas chromatography–mass spectrometry analysis showed that oxidized volatile compounds, such as pentanal, hexanal, heptanal, octanal, 1‐penten‐3‐one, (Z)‐4‐heptenal, (E, E)‐2,4‐heptadienal, and (E)‐2‐octenal, were less developed in the powdered milk containing FeLf than in that containing iron (II) sulfate. Iron and lactoferrin (Lf) were retained in the high‐molecular‐weight (>10000 Da) fraction of the reconstituted FeLf‐containing powdered milk after its manufacture and storage, whereas the antigenicity of Lf was lost after ultrahigh‐temperature processing at 120 °C for 5 s. These results suggest that FeLf reduces the iron‐catalyzed off‐flavors that develop during the production and storage of powdered milk. The stable iron‐holding property of FeLf contributes to the inhibition of oxidized and metallic volatile formation, although the loss of Lf antigenicity did not affect the stability of FeLf and the iron‐catalyzed formation of off‐flavors in the powdered milk. Consequently, FeLf is a suitable candidate for the simultaneous supplementation of a single food with iron and fish oil. Practical Application: The supplementation of food products with iron and fish oil is a useful approach to redressing their inadequate intake in many populations. The iron–lactoferrin complex can protect food products against the off‐flavors caused by iron‐catalyzed lipid oxidation. Our results show that the iron–lactoferrin complex is useful for the simultaneous fortification of foods and nutraceuticals with iron and fish oil because this complex also reduces the formation of iron‐catalyzed off‐flavors in powdered milk enriched with fish oil.     

Chemical, physical, and sensory properties of dairy products enriched with conjugated linoleic acid

Recent studies have illustrated the effects of cis-9,trans-11 conjugated linoleic acid (CLA) on human health. Ruminant-derived meat, milk and dairy products are the predominant sources of cis-9,trans-11 CLA in the human diet. This study evaluated the processing properties, texture, storage characteristics, and organoleptic properties of UHT milk, Caerphilly cheese, and butter produced from a milk enriched to a level of cis-9,trans-11 CLA that has been shown to have biological effects in humans. Forty-nine early-lactation Holstein-British Friesian cows were fed total mixed rations containing 0 (control) or 45 g/kg (on dry matter basis) of a mixture (1:2 wt/wt) of fish oil and sunflower oil during two consecutive 7-d periods to produce a control and CLA-enhanced milk, respectively. Milk produced from cows fed the control and fish and sunflower oil diets contained 0.54 and 4.68 g of total CLA/100 g of fatty acids, respectively. Enrichment of CLA in raw milk from the fish and sunflower oil diet was also accompanied by substantial increases in trans C18:1 levels, lowered C18:0, cis-C18:1, and total saturated fatty acid concentrations, and small increases in n-3 polyunsatu-rated fatty acid content. The CLA-enriched milk was used for the manufacture of UHT milk, butter, and cheese. Both the CLA-enhanced butter and cheese were less firm than control products. Although the sensory profiles of the CLA-enriched milk, butter, and cheese differed from those of the control products with respect to some attributes, the overall impression and flavor did not differ. In conclusion, it is feasible to produce CLA-enriched dairy products with acceptable storage and sensory characteristics.     

Effect of Crystalline Structure on Oxidation of Fish Oil in Stearin:Fish Oil Mixtures

Effects of incorporation of stearin fraction into fish oil on crystallisation behaviour and oxidative stability of fish oil were examined. The stearin fraction (S₂₅) was obtained from step-wise dry fractionation of anhydrous milk fat at 25 °C. Analysis of fatty acid composition by gas chromatography showed that unsaturated fatty acids (89.3 %) were enriched in the fish oil whereas the S₂₅ typically comprises of saturated fatty acids (79.4 %). A series of S₂₅:fish oil mixtures (0:100, 25:75, 50:50, 75:25; 90:10 and 100:0) was prepared by mixing the S₂₅ and fish oil at 50 °C under flushing of nitrogen gas. Crystallisation and thermal properties and crystal structures of the mixtures were investigated by differential scanning calorimetry and small- and wide-angle X-ray scattering, respectively. The crystallisation/melting temperatures and crystallisation/melting enthalpies of the mixtures increased with increasing ratios of S₂₅ blended into fish oil. All mixtures showed similar crystal structures (double- and triple-chain length) and crystal polymorphs (α, β’ and β) at 4 °C. A decrease in S₂₅ fraction in the mixtures caused a higher proportion of triple-chain length crystal packing and β polymorph. Measurement of peroxide values of the mixtures upon storage at 8 °C for 42 days showed that blending as low as 25 % S₂₅ sufficiently delayed the lipid oxidation of fish oil by about two-fold and the rancidity threshold to 16 days instead of 9 days for fish oil only. This study demonstrates that mobility of oxygen and triacylglycerol (TAG) molecules in fish oil can be restricted by crystalline state of milk fat, in turn, limiting the propagation of oxidative reaction in fish oil.     

Age Gelation,Sedimentation, and Creaming in UHT Milk: A Review

Demand for ultra‐high‐temperature (UHT) milk and milk protein‐based beverages is growing. UHT milk is microbiologically stable. However, on storage, a number of chemical and physical changes occur and these can reduce the quality of the milk. These changes can be sufficiently undesirable so as to limit acceptance or shelf life of the milk. The most severe changes in UHT milk during storage are age gelation, with an irreversible three‐dimensional protein network forming throughout, excessive sedimentation with a compact layer of protein‐enriched material forming rapidly at the bottom of the pack, and creaming with excessive fat accumulating at the top. For age gelation, it is known that at least two mechanisms can lead to gelation during storage. One mechanism involves proteolytic degradation of the proteins through heat‐stable indigenous or exogenous enzymes, destabilizing milk and ultimately forming a gel. The other mechanism is referred to as a physico‐chemical mechanism. Several factors are known to affect the physico‐chemical age gelation, such as milk/protein concentration, heat load during processing (direct compared with indirect UHT processes), and milk composition. Similar factors to age gelation are known to affect sedimentation. There are relatively few studies on the creaming of UHT milk during storage, suggesting that this defect is less common or less detrimental compared with gelation and sedimentation. This review focuses on the current state of knowledge of age gelation, sedimentation, and creaming of UHT milks during storage, providing a critical evaluation of the available literature and, based on this, mechanisms for age gelation and sedimentation are proposed.     

疏水改性藜麦淀粉的制备及其Pickering乳液乳化性研究

本文用碱提法从藜麦种子中提取藜麦淀粉,并用辛烯基琥珀酸酐(Octenyl Succnic Anhydride,OSA)对提取的藜麦淀粉进行疏水改性,得到了辛烯基琥珀酸淀粉酯(OSA淀粉)。通过傅里叶红外光谱、扫描电子显微镜对比原淀粉和OSA淀粉颗粒的结构和形态,发现OSA基团成功接到淀粉表面,在形态上表现为颗粒表面轻度破坏。通过测定乳液微观结构,乳滴粒径及乳化指数(EI),分析了OSA淀粉取代度、颗粒浓度和油相比例等因素对Pickering乳液乳化性的影响。结果表明,乳滴粒径随OSA淀粉取代度或淀粉颗粒浓度的增加而减小、EI值随OSA淀粉取代度或淀粉颗粒浓度的增加而提高,乳液乳化性增强。当油相比例的增加时,乳滴粒径增大,且在食品添加剂允许OSA添加量的范围内,取代度为1.43%的OSA淀粉颗粒的EI值达到最大值75.48%,乳化性最好。研究表明OSA改性藜麦淀粉作为Pickering乳液的稳定颗粒在食品领域有极大的应用潜力。     

Impact of chitosan and oregano extract on the physicochemical properties of microencapsulated fish oil stored at different temperature

Fish oil is an excellent source of omega-3 fatty acids and is easily susceptible to oxidation. Microencapsulation is a commonly employed technique to protect fish oil against oxidation. In the present study, the potential of chitosan in combination with bovine gelatin and maltodextrin as wall material for microencapsulation of fish oil by spray drying was evaluated. To improve the oxidative stability of the fish oil microencapsulates, oregano (Origanum vulgare L) extract was added at 0.50 g/100 g of emulsion. The spray-dried powder showed a moisture content of 2.8 – 3.2 g/100 g of spray-dried powder. The powder contained spherical microparticles with different sizes as indicated by scanning electron microscope images. Encapsulation efficiency of microencapsulates ranged between 68.94% and 81.88%. Differential scanning calorimetry and Fourier-transformed infrared spectroscopy analysis of microencapsulates revealed the possible structural stabilization of core and wall material. The oxidative stability of fish oil microencapsulates were monitored under three different temperature (60°C, 28 ± 2°C, and 4°C). Incorporation of oregano extract minimized the generation of secondary and tertiary oxidation products as indicated by lower peroxide value and thiobarbituric acid reactive substance values compared to control. Overall, the results suggested that combination of chitosan along with bovine gelatin and maltodextrin as wall material improved the surface morphology of the microparticle and encapsulation efficiency, whereas incorporation of oregano extract in fish oil before spray drying enhanced the oxidative stability during storage.     

Influence of Emulsification Technique and Wall Composition on Physicochemical Properties and Oxidative Stability of Fish Oil Microcapsules Produced by Spray Drying

Encapsulation of fish oil is an effective way to protect it against oxidation and masking its fishy odor. One of the possible ways to produce fish oil microcapsules is to produce an oil-in-water (O/W) emulsion followed by spray drying. This study compares the production of the O/W emulsion by mechanical homogenization (rotor–stator) with membrane emulsification and examines the effect of the type and amount of wall material added before drying. The membrane emulsification process selected for the emulsion production is premix membrane emulsification (ME), which consists of the production of a coarse emulsion by mechanical means followed by droplet breakup when the coarse emulsion is forced through a membrane. The emulsions produced had an oil load of 10 and 20 % and were stabilized using whey protein (isolate and hydrolyzate at 1 or 10 %) and sodium caseinate with concentrations of 2 and 10 %. Regarding the material used to build the microcapsule wall, whey protein, maltodextrin, or combinations of them were used at three different oil/wall ratios (1:1, 1:2, 1:3). The results clearly show that premix ME is a suitable technology for producing O/W emulsions stabilized with proteins, which have a smaller droplet size and are more monodisperse than those produced by rotor–stator emulsification. However, protein concentrations of 10 % are required to reduce the droplet size down to 2–3 μm. Small and monodisperse emulsions have been found to produce microcapsules with lower surface oil content, which increases oil encapsulation efficiency and presents lower levels of oxidation during storage at 30 °C. Of all the possible combinations studied, the one with the highest oil encapsulation efficiency is the production of a 20 % O/W emulsion stabilized with 10 % sodium caseinate followed by the addition of 50 % maltodextrin and drying.     

Oxidative stability of fish oil enriched drinking yoghurt

The oxidative stability of fish oil enriched drinking yoghurt as well as the antioxidative effect of citric acid ester, vitamin K and disodium ethylenediaminetetraacetic acid (EDTA) were investigated by measuring peroxide value and volatile secondary oxidation products and by sensory analysis. No oxidation was observed in yoghurt stored at 2 °C for up to 19 days, with or without addition of citric acid ester. Fish oil enriched yoghurt was also very stable even when compared to yoghurt with added rapeseed oil or a mixture of rapeseed oil and fish oil stored for up to 29 days. The addition of 50 μm iron to yoghurt did not promote oxidation. The results obtained may indicate an antioxidative effect of EDTA and pro-oxidative effect of vitamin K. All yoghurts had similar viscosity and droplet size. In summary, fish oil enriched drinking yoghurt is very stable towards oxidation.     

植物乳杆菌CICC 20270微胶囊的制备及其特性

以植物乳杆菌CICC 20270(Lactobacillus plantarum)及椰子油/玉米油为芯材,添加到以葡萄糖值即DE值分别为25、18糖浆为壁材的乳状液中,通过喷雾干燥法制备益生菌微胶囊,考察微胶囊的菌细胞存活率、表面结构、耐热性、储藏稳定性及在模拟胃肠液中的菌细胞存活率情况。结果表明:制得的微胶囊中植物乳杆菌存活率均在90%以上。在55℃热处理条件下,各微胶囊菌活无显著性差异(p>0.05);65℃处理1、10 min后,活菌数最低的分别是DE25/椰子油和DE18/椰子油微胶囊,存活率为75.66%、49.82%;75℃热处理1、10 min后,DE18/椰子油微胶囊中活菌数均最低,存活率分别为38.40%、15.08%。在4、25、37℃储藏条件下,玉米油微胶囊储藏性质较椰子油更为稳定,活菌数更高;而在33%、52%、75%湿度条件下,糖浆的DE值不同比油脂对益生菌的存活率影响更大,且DE25糖浆给益生菌提供了更好的保护效果。在6 h体外模拟消化中,DE25糖浆/椰子油微胶囊整个过程活菌数只下降了3.88 lg CFU/g。因此,DE25糖浆更适作为益生菌壁材;添加玉米油后使得微胶囊具有更好的耐热性;而添加椰子油更有利于提高微胶囊在模拟胃肠液中的菌活数。     

Electrophoretic characterization of protein interactions suggesting limited feasibility of accelerated shelf-life testing of ultra-high temperature milk

Accelerated shelf-life testing is applied to a variety of products to estimate keeping quality over a short period of time. The industry has not been successful in applying this approach to ultra-high temperature (UHT) milk because of chemical and physical changes in the milk proteins that take place during processing and storage. We investigated these protein changes, applying accelerated shelf-life principles to UHT milk samples with different fat levels and using native- and sodium dodecyl sulfate-PAGE. Samples of UHT skim and whole milk were stored at 20, 30, 40, and 50°C for 28 d. Irrespective of fat content, UHT treatment had a similar effect on the electrophoretic patterns of milk proteins. At the start of testing, proteins were bonded mainly through disulfide and noncovalent interactions. However, storage at and above 30°C enhanced protein aggregation via covalent interactions. The extent of aggregation appeared to be influenced by fat content; whole milk contained more fat than skim milk, implying aggregation via melted or oxidized fat, or both. Based on reduction in loss in absolute quantity of individual proteins, covalent crosslinking in whole milk was facilitated mainly by products of lipid oxidation and increased access to caseins for crosslinking reactions. Maillard and dehydroalanine products were the main contributors involved in protein changes in skim milk. Protein crosslinking appeared to follow a different pathway at higher temperatures (≥40°C) than at lower temperatures, making it very difficult to extrapolate these changes to protein interactions at lower temperatures.     

Sensory stability and oxidation of fish oil enriched milk is affected by milk storage temperature and oil quality

The experiments evaluated the influence of fish oil quality and cold storage temperature on the oxidative stability of milk emulsions containing 1.0% w/w milk fat and 0.5% w/w of either a pure fish oil or a fish oil:rapeseed oil mixture. The results showed that it was possible to produce a pasteurised milk product enriched with the important n-3 PUFA from fish oil with acceptable sensory characteristics if (1) the emulsions were based on a mixture of fish oil and rapeseed oil and (2) the initial peroxide value (PV) of the added oil blend was below 0.5 meq kg⁻¹. The sensory analysis showed a clear distinction between emulsions based on oil with PV 0.1 and 0.5 meq kg⁻¹, whereas the PV and the gas chromatographic (GC) analysis of volatile oxidation products were not sensitive enough to reveal these differences clearly. The GC analyses showed that the onset of formation of the volatiles was earlier with increased storage temperature in the range of 2–9 °C.     

Effects of chitosan and collagen containing α-tocopherol on the oxidative stability in bulk oil and oil-in-water emulsion

To provide efficient antioxidant capacities, proper carriers are needed to protect antioxidants against oxidative stress. Collagen mesh structure or chitosan gel was loaded with α-tocopherol and their effects were evaluated in bulk corn oil or oil-in-water (O/W) emulsion at 60 °C. Added collagen and chitosan enhanced oxidative stability in corn oil and O/W emulsions at 60 °C compared to corn oils without carriers or with addition of α-tocopherol (p < 0.05). Stability of α-tocopherol in corn oil loaded in collagen or chitosan was significantly enhanced compared to that in oils without carriers (p < 0.05). In O/W emulsions, α-tocopherol loaded collagen showed higher antioxidant properties than α-tocopherol loaded chitosan (p < 0.05). Collagen mesh structure and chitosan gel retarded the rates of lipid oxidation efficiently in both food matrices when α-tocopherol was not loaded. Collagen mesh structure and chitosan gel can be useful carriers for α-tocopherol in bulk oil or O/W emulsion.