Microencapsulation of Bioactive Ingredients for Their Delivery into Fermented Milk Products: A Review
Abstract
:1. Introduction
2. Yogurt Fortification with Nano/Microencapsulated Bioactive Ingredients
2.1. Carotenoids and Carotenoids Containing Components
2.2. Phenolic Compounds (Phenolics) Containing Components
2.3. Other Bioactive Components
2.4. Probiotic Microorganisms
3. Kefir Fortification with Nano/Microencapsulated Bioactive Ingredients
4. Cheese Fortification with Nano/Microencapsulated Bioactive Ingredients
4.1. Probiotic Microorganisms
4.2. Phenolic Compounds (Phenolics) Containing Components
4.3. Other Bioactive Components
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
Sample Availability
References
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Bioactive Component | Encapsulation Techniques and Systems | Encapsulant Materials | Observations | References |
---|---|---|---|---|
Tomato peel extract | Electrospinning | Zein, gelatin | Similar properties to control yogurt sample in terms of yogurt acidity, pH, syneresis, and viscosity. The increase of yogurt free radical scavenging activity by 40–60%. | [18] |
Red pepper waste extract | Freeze drying, spray drying | Whey proteins | Fortified yogurt showed higher sensory and general acceptability scores compared to control sample. | [19] |
Red bell pepper extract | Inclusion complexation by ultrasonic homogenization | β-Cyclodextrin | A mean particle diameter was 562 nm. The prepared complexes can simulate the color of papaya flavors. The higher stability of color was observed for yogurt colored with inclusion complexes comparing with yogurt colored with crude extract. | [20] |
Cantaloupe melon extract | Emulsification in O/W followed by lyophilization | Gelatin as a wall material | The solubility of extract encapsulated in gelatin (EG) was 0.072 mg/mL. EG gave homogenous yellow coloration to yogurt; staining was preserved over 60 days. | [21] |
β-Carotene | Spray-dried emulsion followed by fluidized bed coating | Maltodextrin or sodium caseinate for emulsification and hydroxypropyl cellulose for coating. | Coated powders were used for yogurt coloration. After 4 weeks of storage, the changes of yogurt color were minimal. Total color difference ΔE value was < 3. | [22] |
β-Carotene | Multilamellar liposomes obtained by the hydration of proliposomes | Stabilized by the mixture of xanthan and guar gums. | About 90% of the encapsulated β-carotene was preserved after the storage for 95 days at 7–10 °C. Liposomes were tested as colorant in yogurt. Its texture was not affected by the incorporation of the liposomes. | [23] |
β-Carotene | Solid lipid microparticles (SLM) | Palm stearin as the lipid phase and hydrolyzed soy protein isolate for particles stabilization | The average diameter of SLM was 1.2 µm. The amount of 25 g (500 mL) of SLM was added to 10 L of yogurt. The addition of SLM did not change the physicochemical and rheological characteristics of yogurt. Based on sensory analysis, the average grade of global acceptance was 7.4 (“liked it very much”) on the hedonic scale. | [24] |
β-Carotene | Spray drying; coacervation for beads | Maltodextrin for spray drying Chitosan and alginate for beads | In yogurt, spray-dried β-carotene showed higher release and the incorporation into micelle phase during digestion than β-carotene encapsulated in chitosan–alginate beads. | [25] |
Zeaxanthin | Nanoemulsion by high-pressure homogenization | Zeaxanthin was dispersed in chia seed oil. Tween 80 for emulsification. | After 28 days of yogurt storage, zeaxanthin retention was 16.84%. Higher bioaccessibility as compared to zeaxanthin nanoparticles. | [26] |
Zeaxanthin | Nanoparticles | Cactus mucilage as a wall material. Zeaxanthin was dispersed in chia seed oil. | After 28 days of yogurt storage, zeaxanthin retention was 22.31%. The incorporation of zeaxanthin nanoparticles decreased the texture and viscosity and increased the syneresis when compared to the control yogurt. The changes were not sensory perceived. | [26] |
Astaxanthin | Beads prepared using ultrasonic atomizer | Alginate and chitosan | The concentration of beads in yogurt was 15% (w/w). No differences were observed for the appearance, color, and aroma as compared to control yogurt. Consumers perceived differences in terms of taste, mouthfeel, and overall liking attributes. | [27] |
Lipid extract of astaxanthin from shrimp waste | Complex coacervation with following freeze drying. | Gelatin and cashew gum | Coloring capacity of microcapsules was compared to non-encapsulated lipid extract. Both forms of astaxanthin yielded the orange color of yogurt. Encapsulated form showed more intense color. No differences in odor between the yogurt sample containing encapsulated lipid extract and the sample containing non-encapsulated lipid extract were found. | [28] |
Palm oil | Coacervation | Chitosan and carboxymethylcellulose | Particles showed the ideal carotenoid release in gastric fluid, but low release in the intestinal fluid, which increased when applied to yogurt. | [29] |
Palm oil | Ionic gelation | Chitosan plus sodium tripolyphosphate as a cross-linker | Particles showed high carotenoid release in gastric fluid, but satisfactory release in intestinal fluid. The release further increased when the particles were added to yogurt. | [29] |
Palm oil | Coacervation followed by lyophilization | Chitosan and xanthan; chitosan and pectin | Chitosan/xanthan microparticles applied in yogurt released approximately 50% of the content in the intestinal fluid. The behavior of release was similar to the desired one. The release of content from chitosan/pectin microparticles was slower. | [30] |
Bioactive Component | Encapsulation Techniques and Systems | Encapsulant Materials | Observations | References |
---|---|---|---|---|
Grape seed extract | Spray drying | Whey proteins and gum arabic | The addition of encapsulated grape seed extract at the final concentration of 1% resulted in similar sensory properties, viscosity, acidity, water-holding capacity, and color compared to the control. The antioxidant activity increased four-fold. | [34] |
Orange peel extract | Coacervation | Whey proteins and gum arabic | The negative influence on the physicochemical and organoleptic properties of yogurt was not observed. | [39] |
Sour cherry extract | Spray-dried coated liposomes | Lecithin for liposomes preparation and chitosan for their coating. | Liposomal powders (LP) were added to yogurt with a ratio of 5% (w/w). The addition of LP did not change the color parameters of yogurt up to 14 days of storage. Encapsulation provided the stability of extract in terms of total phenolic content and antioxidant capacity. | [35] |
Doum extract | Coated liposomes | Lecithin for liposomes preparation and chitosan for their coating. | Naringenin was the main component of extracted phenolics. Yogurt fortified with 5% of liposome solution had similar characteristics including the acidity, water-holding capacity, and texture parameters as a control yogurt, but the antioxidant activity was higher. The addition of higher percentage of encapsulated product affected markedly the functional properties of yogurt. | [36] |
Cocoa hull waste extract | Spray-dried coated liposomes | Lecithin for liposomes preparation and chitosan for their coating. | For yogurt fortification, liposomes in two forms, i.e., dispersion and sprayed-dried powders, were used. The best results were found for the powder form in terms of total phenolic compounds and total antioxidant activity. | [37] |
Hibiscus calyx extract | Double emulsion and following ionic gelation. | Rapeseed oil and pectin | The extract is rich in anthocyanins. Microparticles were obtained by dripping-extrusion and atomization methods. The microparticles were added to yogurt with a ratio of 20% (w/w). The yogurt supplemented with microparticles obtained by atomization had higher appearance acceptability, but the retention of bioactive compounds was lower comparing to dripping techniques. | [40] |
Tartary buckwheat extract | Beads were prepared by thermally-induced polymerization of proteins and following spray drying. | Whey proteins | The extract is rich in rutin and quercetin. Yogurt contained 3% (w/w) of beads. Encapsulation masked the dark yellow color and bitter taste of extract and protected flavonoids from the gastric juice. | [45] |
Olive leaves extract | Nanoliposomes | Lecithin and cholesterol with the ratio of 4:1. | The extract is rich in oleuropein. The amount of 100 g yogurt was fortified with 15 g (containing 10% of phenolics) of nanoliposomes. No changes in color and sensorial attributes were observed. The antioxidant activity did not change during the yogurt storage for 21 days. | [44] |
Eggplant (Solanum melongena L.) bark extract | Spray drying | Gum arabic | The extract is rich in anthocyanins. The amount of 1, 1.5, and 2 g of encapsulated and nonencapsulated extract was added to 100 g of yogurt. More than 50% of free anthocyanins degraded in yogurt after 20 days of storage, whereas encapsulated ones remained stable. The decrease of antioxidant activity was slower for yogurts fortified with the encapsulated form of extract. | [38] |
Date palm pollen | Nanocapsules obtained by ultrasonication | Sodium caseinate and lecithin | The extract is rich in catechin. The size of capsules was approximately in the range of 200–300 nm. The amount of pollen extract in free and encapsulated form was 0.75% (w/v) of milk. No color changes were observed for yogurt fortified with encapsulated pollen extract. It also scored the higher scores of appearance and body and texture compared to yogurt fortified with free extract. Overall, sensorial acceptability was also higher. | [41] |
Resveratrol | Niosomes | Surfactants sorbitan monostearate (S60), labrasol (Lab) and maisine 35-1(Mai), and lauryl alcohol (Dod) as stabilizer | Niosomes were prepared by thin film hydration method. About 10% (v/v) of niosomes suspension was added to yogurt. The texture parameters (firmness and adhesiveness) of yogurt fortified with Mai-Dod and S60-Dod niosomes were the same as of control ones. Yogurt enriched with Lab-Dod niosomes showed the decrease in the adhesiveness. | [42] |
Cheese Type | Microorganism | Encapsulation Techniques and Systems | Encapsulant Materials | Observations | References |
---|---|---|---|---|---|
Cream cheese | Lactobacillus rhamnosus | Microgel particles obtained by aerosol spraying | Sodium alginate | L. rhamnosus remained viable (min 106 CFU/g) over 35 days of storage at 4 °C. The addition of encapsulated probiotic bacteria resulted in a firmer and thicker cheese. | [102] |
White brined cheese | Lactobacillus rhamnosus | Microcapsules obtained by cold gelation | Maillard reaction products of isomaltooligosaccharides and whey proteins | Droplet-like capsules with a smooth surface, whose diameter was approximately 183 μm. The viability of encapsulated probiotic was increased compared to free cells during 90 days of storage at 4 °C. Sensory properties of cheese were not affected by the addition of encapsulated bacteria. | [103] |
White brined cheese | Bifidobacterium bifidum, Lactobacillus acidophilus | Extrusion, emulsion | Sodium alginate for extrusion and corn oil and κ-carragenan for emulsion | Both techniques were effective in keeping cell counts higher than the therapeutic minimum during 90 days of storage at 4 °C. The content of free fatty acids, acetaldehyde, and diacetyl was higher as compared to control sample. | [104] |
Iranian UF Feta cheese | Lactobacillus paracasei | Enzyme based gelation (rennet or transglutaminase) | Sodium caseinate or skim milk powder | The cells entrapped into microcapsules by rennet-based gelation exhibited the higher viability compared to transglutaminase-based gelation. | [105] |
Iranian UF white cheese | Lactobacillus plantarum | Complex coacervation followed by spray drying or freeze drying | Whey protein isolate and gum arabic | Phytosterol was coencapsulated with bacteria. Its coencapsulation increased the viability of bacteria in cheese during 91 days of storage at 4 °C in comparison with encapsulated bacteria alone or free cells. | [106] |
Iranian white brined cheese | Lactobacillus acidophilus | Extrusion | Calcium alginate and resistant starch | The survival of bacteria was increased in cheese and was equal to ≥107 CFU/g after 6 months of storage. | [107] |
Iranian UF white cheese | Lactobacillus plantarum,Bifidobacterium bifidum, Lactobacillus casei subsp. casei | Extrusion | Sodium alginate | After 60 days of cheese storage at 8–10 °C, the counts of each encapsulated bacterium were higher than the therapeutic minimum (106–107 CFU/g). | [108] |
Cheddar cheese | Bifidobacterium bifidum | Emulsification/internal gelation | κ-carrageenan or sodium alginate | For encapsulated bacteria, the decrease of viability was slower over a period of 35 days. The encapsulant sodium alginate showed the better results than κ-carrageenan under simulated gastrointestinal conditions. | [109] |
Cheddar cheese | Bifidobacterium longum | Co-axial droplet extrusion, emulsification/internal gelation | Sodium alginate or palmitoylated alginate | After 21 days of cheese storage at 4 °C, bacteria encapsulated by emulsification/internal gelation showed 2 log CFU/mL reduction as compared to free cells with 4 log CFU/mL reduction. | [110] |
Kariesh cheese | Bifidobacterium adolescentis | Rennet based gelation | Milk proteins | The viability of encapsulated bacteria increased during two weeks of cheese cold storage. | [111] |
Mozzarella cheese | Lactobacillus paracasei | Emulsification/internal gelation | Sodium alginate | Encapsulation provided no protection against simulated gastric juice. | [112] |
Soft goat cheese | Lactobacillus plantarum | Spray drying | Skim milk | After 8 weeks of cheese storage, the high level of 8.82 log CFU/g was found for the encapsulated bacteria, while the free-cell number decreased to 6.9 log CFU/g. The addition of spray-dried bacteria did not change the properties of cheese (pH value, chemical composition, sensory quality). | [113] |
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Gruskiene, R.; Bockuviene, A.; Sereikaite, J. Microencapsulation of Bioactive Ingredients for Their Delivery into Fermented Milk Products: A Review. Molecules 2021, 26, 4601. https://doi.org/10.3390/molecules26154601
Gruskiene R, Bockuviene A, Sereikaite J. Microencapsulation of Bioactive Ingredients for Their Delivery into Fermented Milk Products: A Review. Molecules. 2021; 26(15):4601. https://doi.org/10.3390/molecules26154601
Chicago/Turabian StyleGruskiene, Ruta, Alma Bockuviene, and Jolanta Sereikaite. 2021. "Microencapsulation of Bioactive Ingredients for Their Delivery into Fermented Milk Products: A Review" Molecules 26, no. 15: 4601. https://doi.org/10.3390/molecules26154601
APA StyleGruskiene, R., Bockuviene, A., & Sereikaite, J. (2021). Microencapsulation of Bioactive Ingredients for Their Delivery into Fermented Milk Products: A Review. Molecules, 26(15), 4601. https://doi.org/10.3390/molecules26154601