Fatemeh Karegar; Rezvan Pourahmad; Peyman Rajaei
Abstract
[1]Introduction: Nowadays, with the development of probiotic products on the world market, the need for developing new products containing probiotic bacteria becomes more apparent. Probiotics are defined as living microorganisms that, if consumed in sufficient quantities, will have beneficial effects ...
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[1]Introduction: Nowadays, with the development of probiotic products on the world market, the need for developing new products containing probiotic bacteria becomes more apparent. Probiotics are defined as living microorganisms that, if consumed in sufficient quantities, will have beneficial effects on the health of the host. Probiotics are now widely used in the production of food products and account for approximately 65% of functional foods. Probiotics often belong to either the genus Lactobacillus or Bifidobacterium. Lactobacillus rhamnosus is one of the known probiotic bacteria with beneficial properties. Prebiotics are defined as indigestible compounds, mainly carbohydrates that can be used as carbon source for probiotic bacteria and stimulate their growth and viability. Oligofructose is a type of short chain inulin and is one of the most well- known prebiotics. Moreover, microencapsulation of probiotic bacteria can improve the survival of these bacteria. In this approach, living probiotic cells are covered or trapped by various compounds. Hydrocolloids such as alginate and carbohydrates such as starch can be suitable compounds for microencapsulation. The purpose of this study was to investigate the effect of oligofructose and microencapsulation on the viability of Lactobacillus rhamnosus, textural, physicochemical and sensory characteristics of functional jelly. Materials and methods: In this study, different concentrations (0, 1.5 and 3 percent) of oligofructose as prebiotic were used to produce jelly samples, and 107 CFU/mL of probiotic bacteria (free and microencapsulated Lactobacillus rhamnosus) was inoculated. Microencapsulation of probiotic bacteria was performed by emulsion method using sodium alginate and corn resistant starch. The jelly samples were stored at 4˚C for two weeks. pH, acidity, dry matter, firmness, probiotic bacterial count and sensory properties (taste, odor, texture, color and overall acceptance) of the samples were evaluated on the first, 7th and 14th days of jelly production. Seven samples including 6 treatments and 1 control sample (without probiotic bacteria and prebiotic compound) with three replications were studied. The data were subjected to analysis of variance (ANOVA), followed by the Duncan’s multiple range test to determine the significant difference between samples at 95% confidence level (p<0.05) using the SAS 9.4 M4 Software. The charts were drawn by Excel 2013. Results and discussion: The results of sensory evaluation showed that the effect of different percentages of oligofructose on the sensory parameters, except for the taste, was not significant (p>0.05). Using 1.5% oligofructose and probiotic bacteria (free or microencapsulated) did not change the score of taste but the use of 3% oligofructose and free probiotic bacteria decreased the score of this parameter. The effect of storage time on sensory properties (taste, odor, texture, color and overall acceptance) was significant (p<0.05) so that with increasing storage time, the score of sensory parameters decreased. The results of physicochemical tests indicated that with increasing oligofructose, dry matter increased and acidity decreased (p<0.05). The results of texture analysis showed that the microencapsulation of probiotic bacteria and addition of oligofructose significantly (p<0.05) increased the firmness of jelly texture. During storage period, pH and dry matter significantly (p<0.05) decreased but acidity and firmness of jelly texture increased. The results of probiotic bacterial count indicated that the use of microencapsulated probiotic bacteria and oligofructose significantly (p<0.05) increased the survival of Lactobacillus rhamnosus. The viability of probiotic bacterai decreased during storage period, t however, the number of probiotic bacteria in the samples was in the range of 106- 107 CFU/g. On the first and 7th days, no mold and yeast contamination was observed in the samples and on the 14th day, the number of molds and yeasts was less than 10 CFU/g. The sample containing microencapsulated probiotic bacteria and 3% oligofructose (sample 4) was selected as the best sample in terms of probiotic bacterial count and textural, physicochemical and sensory quality. Therefore, it is possible to produce synbiotic jelly with the desired quality
Food Engineering
Hossein Mohebodini; Atefe Maqsoudlou
Abstract
Introduction: Microencapsulation is the most commonly used method of preserving proteins and peptides, which increases the stability in different conditions. Bee pollen with 10–40% protein, is a valuable source of protein that has functional and nutraceutical properties. By hydrolysis and producing ...
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Introduction: Microencapsulation is the most commonly used method of preserving proteins and peptides, which increases the stability in different conditions. Bee pollen with 10–40% protein, is a valuable source of protein that has functional and nutraceutical properties. By hydrolysis and producing bioactive peptides, their functional and health effects will be improved. Fibersol is a dietary fiber that can be used in many foods and supplements. This carbohydrate compound is actually non-digestible maltodextrin and has recently been used as a wall material in encapsulation. Few studies have conducted on the microencapsulation of hydrolysed proteins and their stability during accelerated conditions. On the other hand, by-products of honey bees such as pollen have been less noticed; therefore the aim of this study was the microencapsulation of bioactive bee pollen protein hydrolysate by fibersol and WPC and to study the changes of structure and stability of resulted microcapsules during the exposure to UV radiation. Material and Methods: Bee pollen was hydrolysed by Alcalase (1.5%) for 4 h in shaking incubator. The protein hydrolysate was microencapsulated using WPC, fibersol, and their combination by spray drying. The wall materials and hydrolysed protein were used in ratio of 10:1 (w/w). WPC 2%, fibersol 2%, as well as WPC and fibersol mixtures with 1:3 ratio, were the wall materials. For accelerating the oxidation reactions, the obtained capsules were exposed to UV radiation for 48 h. During the exposure to UV radiation, the DPPH radical scavenging activity of microcapsules and hydrolysed protein was measured. Interactions between hydrolysed protein compounds, WPC and fibersol were identified by the FTIR spectroscopy. The SEM was used to investigate the morphology of the microcapsules. Results & Discussions: Almost at all experimental time, the highest DPPH radical scavenging during exposure to UV radiation was related to the capsules prepared using fibersol and WPC mixture and after that the capsule with WPC as wall material. The FTIR spectroscopy of the hydrolysed protein was changed significantly when it was exposed to UV radiation. This change caused by losing the hydrogen bonds in the secondary structure of proteins, including the separation of two polypeptide chains or the opening of the αhelix and loss of β-sheet structure. The FTIR profile of capsulated hydrolysed protein by fibersol showed that the adhesion of protein and polysaccharide changed the absorbance of C–H bending and N–H stretching bands of amide groups in the hydrolysed protein in 3000–3500 cm-1 and the stretching band of C–H and O–H group in the region of 2000–3000 cm-1 for fibersol in the wall. After exposure to UV, because of cross-linking in fibersol and more involving the molecules of fibersol to protein, the absorbance was increased in the region of 1500–3500 cm-1. The number of peaks and absorbance in the FTIR spectra of hydrolysed proteins microencapsulated in WPC were more than number of peaks and absorbance in the FTIR spectra of WPC. There was no significant difference in the FTIR spectra of hydrolysed protein encapsulated with WPC before and after exposure to UV. The peaks in FTIR spectra of hydrolysed protein microencapsulated with the mixture of WPC and fibersol, showed higher absorbance level than the peaks of fibersol and lower than peaks of WPC. None of the peaks of microencapsuls with the wall of mixture of WPC and fibersol, were changed after exposure to UV radiation. Results of SEM showed that the microcapsules prepared with mix of fibersol and WPC had a uniform and smoother wall than microcapsules prepared with only fibersol. Finally, the mix of WPC and fibersol was selected as the best wall with a proper protective ability for the microencapsulation of hydrolysed proteins and protection against UV radiation.
Forouzan Jalali-zand; Mohammad Goli
Abstract
Introduction: Microencapsulation is represented as a technology of packaging solids, liquids, or gaseous materials in miniature sealed capsules that can release their contents at controlled speeds under specific conditions. The packaged materials can be pure materials or a mix, which are also called ...
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Introduction: Microencapsulation is represented as a technology of packaging solids, liquids, or gaseous materials in miniature sealed capsules that can release their contents at controlled speeds under specific conditions. The packaged materials can be pure materials or a mix, which are also called coated material, core material, actives, internal phase (Fang & Bhandari, 2010). Selenium is a micronutrient essential element for human health, which is toxic in high concentrations. Selenium is a component of selenoproteins that plays an enzymatic and structural roles in human biochemistry. Selenium is known as an antioxidant and catalyzer for active thyroid hormone production. The aim of this study was to optimize the microencapsulation of sodium selenite (100-900 mg per 20 mL final spray solution) using a combination of Arabic gum (25-29% per 20 mL final spray solution) and Persian gum (1-5% per 20 mL final spray solution) as capsule wall applying modified solvent evaporation method to produce microcapsules with the highest encapsulation efficiency (EE) and the smallest possible particle size using the response surface method (RSM) with central composite design (α = 2 with 6 central points and 2 repetition in axial and factorial points). Materials and Methods: In this research, production of encapsulated sodium selenite at different concentration (100, 300, 500, 700 and 900 mg/20 cc) with Arabic gum (25%, 26%, 27%, 28% and 29%) and Analogous Farsi gum (5%, 4%, 3%, 2% and 1%) as wall materials by solvent evaporation method was studied. The optimization of microcapsules based on the highest encapsulation efficiency and smallest microcapsules size was studied using RSM. Based on the mentioned parameters, 2 optimum conditions were chosen. The first one was a condition where the samples produced with 135 mg sodium selenite in 20 ml sprayed solution, 27% and 3% Arabic and Farsi gum, respectively. In this condition the encapsulation efficiency was 79.63% whereas the microcapsules size was 49.98 µm. The second condition was followed by producing samples with 109 mg sodium selenite in 20 ml sprayed solution, 28% and 2% Arabic and Farsi gum with result of 95.10% encapsulation efficiency and the size of 46.71 µm. Finally 390 ppm capsules of the first condition and 480 ppm capsules of second condition (equal to 8.6 ppm sodium selenite salt), synthesized BHA (200 ppm) and sodium selenite salt (8.6 ppm) were added to a free anti-oxidant soybean oil and were kept at 55°C at 0, 23 and 46 days which was equal with 20°C at 0, 180 and 360 days. In this condition, peroxide value, acidity, Thiobarbituric acid, Anisidine value, Totox value and anti-oxidant activity of free anti-oxidant soybean oil were evaluated using SPSS software. Results & Discussion: The results achieved by RSM showed that sodium selenite concentration had reverse relation on encapsulation efficiency whereas there was direct relation with Arabic and Farsi gum concentration. Also the size of microcapsules with had direct relation on sodium selenite concentration whereas Arabic and Farsi gum concentration had reverse relation. The result of SPSS analyses showed that with presence of the encapsulated sodium selenite anti-oxidant and synthesized BHA anti-oxidant in soybean oil, peroxide value, acidity, Thiobarbituric acid, Anisidine value, Totox value decreased whereas anti-oxidant activity of soybean oil increased. Based on anti-oxidant characteristics in soybean oil, recommended treatments in this research are: condition 2 ˃ condition 1 ≥ BHA ˃ sodium selenite salt ˃ control sample without anti-oxidant. The results of this study recommend the incorporation of encapsulated sodium selenite (condition 1 and 2) for increasing the shelf life of soybean oil as an alternative to synthesized BHA.
Seyed Hassan Jalili; Reza Farhoosh; Arash Koocheki; Abbas Ali Motallebi
Abstract
Introduction: Considerable amounts of essential fatty acids in fish oil makes it possible to use in the production of functional foods to meet nutritional needs and beneficial effects on health. One of the major problems is their high susceptibility to oxidative deterioration and consequent production ...
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Introduction: Considerable amounts of essential fatty acids in fish oil makes it possible to use in the production of functional foods to meet nutritional needs and beneficial effects on health. One of the major problems is their high susceptibility to oxidative deterioration and consequent production of undesirable flavor. At present, some synthetic compounds are used as antioxidants in food and biological systems, but the use of synthetic antioxidants is of concern due to their potential health hazards. Therefore, the use of natural antioxidants in foods is the first choice. Enzymatic protein hydrolysis has been applied to food industry by-products to produce foods with enhanced functional properties. Antioxidant and antiradical activity of protein hydrolysates from meat, skin, bone, viscera and roes of various aquatic species has been reported. Silver carp (Hypophthalmichthys molitrix) skin (SCS), as low price by-product from minced products processing plants is available in I.R. Iran. Amino acids composition and sequencing determines the functional properties of peptides, which depends on the source of protein, the method and conditions of preparation and molecular weight distribution of resulting hydrolysate. The enzyme type and hydrolysis conditions, including enzyme/substrate ratio, temperature, time and pH, can affect the peptides length and functional properties of protein hydrolysates. The effects of hydrolysate from SCS hydrolyzed by alcalase on some quality features and oxidative stability of microencapsulated Kilka (Clupeonella spp.) oil at pH 6.8 and 3.4 were investigated. Materials and methods: SCS was pre-treated with NaOH and acetic acid, washed and freeze dried. Proteolysis with alcalase (1% w/w) at 50 ºC, without pH adjustment, was performed for 4 hours with gentle stirring. Enzyme inactivated by placing the sample in a boiling water bath for 15 minutes. After centrifugation at 13000 g for 20 minutes, supernatant was removed as silver carp skin hydrolysate (SCSH) and freez dried. Emulsions were prepared with 31.25% dry material. 25% of wall materials (equal proportions of maltodextrin and Hi-Cap®100), fish oil 25% and SCSH (for preparing 1, 2, 3, 4 and 5 mg/mL treatments) in two adjusted pH 3.4 and 6.8, was used. Fish oil was refined using multi-layered column chromatography (alumina-silica gel), and fatty acid composition was determined. The emulsion pre-homogenized by the IKA Ultra-turrax at 15,000 rpm for 2 minutes and finally by a HSTO homogenizer at 350 bar for 5 circle, to produce microemulsion. Effects of treatments on the characteristics and oxidative stability of microencapsulated Kilka oil for 28 days in the dark at 45 ºC were compared by determination of surface oil, microencapsulation efficiency, free oil, emulsion stability (%separation), droplet size, optical microscopic observation of morphology and peroxidation stability. Results & discussion: Results showed significant differences between proximate composition of silver carp skin, before and after pre-treatment and revealed that applied method and conditions reduced the amounts of oil and ash to an acceptable level. No aggregation and cluster formation was observed in optical microscopic images of prepared emulsions. The effects of pH on the droplet size and microencapsulation efficiency were insignificant (p> 0.05), but the amount of free oil and emulsion stability were significant at ≥2 mg/mL concentrations of hydrolysate (p<0.05). Peptides effectively retarded the preoxidation of Kilka oil in the model system. Hydrolysate antioxidant power was dose dependent. Peroxidation trends were nonlinear for control and 1-4 mg/mL treatments. These trends continued linearly, with mild slope for 5 mg/mL, and was similar for 2 pH during 28 days. Hydrolysate of SCS may be used as a natural antioxidant for the production of stable microencapsulated fish oil for the enrichment of various kinds of beverages with a wide range of pH.
Nasrin Malekizadeh; Seyed Hadi Peighambardoust; Aref Oladghaffari; Khashayar Sarabandi
Abstract
Introduction: Sumac is the common name of the Rhus genus, which contains over 250 individual species in the Anacardiaceae family. It is grown in temperate and tropical regions worldwide.Sumac is one of the most common spices used by people of the Mediterranean and Middle East regions. The sumac berries ...
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Introduction: Sumac is the common name of the Rhus genus, which contains over 250 individual species in the Anacardiaceae family. It is grown in temperate and tropical regions worldwide.Sumac is one of the most common spices used by people of the Mediterranean and Middle East regions. The sumac berries contain flavones, tannins, anthocyanins, and organic acids which provide antioxidant, antimicrobial and hypoglycemic activities. Due to spices maintenance problems caused by growth of microorganisms, flavor and color compounds losses, using spices extracts have recently been replaced. Although spices extract is sensitive to light, heat and oxygen and have a lower shelf life in poor storage conditions. Therefore, spices extract microencapsulation has been suggested by researchers. Spray drying is the most common and economical methods of microencapsulation. The aim of this study was to investigate the influence of different concentrations of maltodextrin and inlet air temperature on some properties of encapsulated sumac extract.
Materials and Methods: In the present study, the effects of three different inlet air temperatures (140, 160 and 180°C) and three different maltodextrin (DE=20-18) concentrations (10, 20 and 30%) on production efficiency, moisture content, water activity, solubility, hygroscopicity, wettability and color parameters of sumac extract spray dried powder were investigated. In all experiments, outlet air temperatures, atomizer rotational speed, feed flow rate and atomizer air pressure were kept constant at 80°C, 18000 rpm, 20 ml/min and 4±0.1 bar, respectively.
Results and Discussion: Production yield of the sumac powders varied from 44 to 57%. The addition of maltodextrin increased the product yield by preventing adhesion of the sumac extract on the dryer walls and also increasing the inlet air temperature caused an increase in product yield (P
Layla Zaghari; Alireza Bassiri; Somaye Rahimi; Ali Zonousi
Abstract
Intoduction: Probiotics are defined as essential live microorganisms that, when administered in adequate amounts, confer a health benefit on the host. The range of beneficial properties reaches from lowering cholesterol to preventing cancer. The most important probiotic microorganisms belong to the group ...
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Intoduction: Probiotics are defined as essential live microorganisms that, when administered in adequate amounts, confer a health benefit on the host. The range of beneficial properties reaches from lowering cholesterol to preventing cancer. The most important probiotic microorganisms belong to the group of lactic acid bacteria. Lactobacillus reuteri which naturally occurs in the human intestine possess probiotic properties with good colonization potential. The development of probiotic foods presents many challenges, particularly with respect to the stability of the bioactive compounds during processing, storage and passage through acidic gastric environment. Therefore, it is a great challenge to bring the probiotics into a stable form, which guarantees, that the microorganisms reach their target location, the human intestine, in an adequate amount. Microencapsulation helps improve survival probiotic bacteria from environmental stresses. In most studies, probiotic bacteria are entrapped in a gel matrix of natural biological materials such as alginate, or gellan. The core and wall solutions are turned into drops of the desired size by employing an emulsion method. The main problem in the probiotic entrapment approach is that gel bead entrapment technologies generally stabilize the bacteria in liquid products and are difficult to scale up. In order to extend the shelf life of encapsulated probiotics, a glassy state form of the embedding matrix is required. This can be achieved by employing such as air-suspension fluidized-bed coating. In the present research, an air-suspension fluidized-bed technique for generation of core and shell microcapsules containing probiotic Lactobacillus reuteri cells and the efficacy of shellac and sodium alginate at different concentrations on viability of capsules in simulated gastrointestinal conditions was evaluated.
Materials and methods: Pure freeze-dried Lactobacillus reuteri PT-1655 were obtained from Persian Type Culture Collection (Tehran, Iran) and were activated by inoculation in the MRS broth at 37°C for 36-48 h. The air-suspension process was performed in a Wurster coater system with a bottomspraying atomizer. The growth curve of lactobacillus reuteri were determined by measuring the optical density (turbidity) at 600 nm to estimate the time when the growth curve enters a stationary phase in which bacteria develop a general stress resistance and are thus more resistant to various types of stresses. In various pretests the fluidization pressure, the atomization pressure and the spraying rate of the microencapsulation process were varied to examine their influence on process conditions, especially on the particle development. Several different solutions of Lactobacillus reuteri were prepared and evaluated for percentage survival during the coating. The solution containing Lactobacillus reuteri (6–12 g/100 g solution), maltodextrin (4–7 g/100 g solution) and sorbitol (4–7 g/100 g solution) concentrations was spray-coated at three inlet temperatures: 37, 47 and 62°C onto and absorbed by the inert carrier microcrystalline cellulose to produce nonagglomerating dry coated. For the coating processes an aqueous shellac solution at 3 concentrations (16, 17 and 18% (w/v)), containing plasticizers in the ratios of 95 + 5 and an aqueous sodium alginate solution at 3 concentrations (0.5, 1 and 1.5% (w/v)), were used. Simulated gastric juice was prepared fresh daily containing 3.2 mg of pepsin, 1 ml of NaCl solution (0.5%) and acidified with HCl (1.2 M) to pH 1.5 ± 0.5. Tolerance to gastric juice was examined by placing freshly prepared cells in a tube containing sterile simulated gastric juice for 1 h and incubated at 37°C for 2 h. To characterize the morphology of the MCC particles coated with the different matrix formulations, SEM images were taken. Experimental data have been represented as the mean with standard deviation (SD) of different independent determinations. The significance of differences was evaluated by analysis of variance (ANOVA). Differences were considered statistically significant at p
Setareh Hosseinzadeh; Mohammad Hossein Hadad Khodaparast; Aram Bostan; Mohebbat Mohebbi
Abstract
Introduction: Flavor plays a pivotal role in consumer satisfaction and further consumption of foods. Most available aroma compounds are synthetic and most of consumers tend to avoid them as they are of the idea that the chemical flavors are toxic or detrimental to their health. Recently, the market of ...
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Introduction: Flavor plays a pivotal role in consumer satisfaction and further consumption of foods. Most available aroma compounds are synthetic and most of consumers tend to avoid them as they are of the idea that the chemical flavors are toxic or detrimental to their health. Recently, the market of flavors from natural sources is shifting its focus on application rather than synthetic flavors (Badee et al, 2012). Essential oils consist of sensitive compounds against environmental effects. Microencapsulation is one of the methods which increases the stability of essential oils and flavors during storage and transportation. Different methods which may be used for microencapsulation include spray drying, spray-cooling, spray-chilling, coaservation, extrusion, fluidized bed method (KashappaGoud et al, 2003). However, spray drying method is preferred due to its high speed, high reliability, high flexibility and its being economical and the fact that it can be easily implemented in industry (KashappaGoud et al, 2003). Spray drying of essential oils requires homogenizer, spray dryer and chemical materials used for walls such as some types of emulsifiers and ingredients including maltodextrin, dried corn syrup, gum Arabic, gelatin and milk protein (Adamiec&Kalemba, 2004; Badee et al, 2012). Arabic gum (acacia gum) is a biopolymer which is derived from internal sap of acacia tree. It consists of a heteropolysaccharide complex with highly ramified structure (Phisut, 2012). It is an effective emulsifier for flavor emulsions thanks to its high water solubility, low solution viscosity, good surface activity, and ability to form a protective film around emulsion droplets (Chanamai&Mcclements, 2001). Maltodextrins are products of starch hydrolysis, consisting of D-glucose units linked mainly by α(1→4) glycosidic bonds. They are described by their dextrose equivalence (DE) which is inversely related to their average molecular weight. The greater the DE is, the shorter the glucose chains are and the more water they absorb (Phisut, 2012). Materials and method: Spearmint oil was produced by clevenger distillation from spearmint leaves (Mohal Khan et al, 2012). Malthodextrin with DE=18-20 from Xiwang Starch Co. Ltd., China, has a sweet taste and it is used in combination with emulsifiers, creates the walls and covers and causes thermal resistance and resistance to browning. Solubility in water=min 98%, moisture=4.5-6%, pH=4.5-6.5 and ash=max 0.1%. Arabic gum was prepared from Slandwide Corporation Co., Philippines, which is used as an emulsifier, stabilizer and the cover (moisture = max 10%, ash=max4% and pH =4-5).In making an emulsion, deionized double distilled water was used.A Solution of maltodextrin/arabic gum (1:1) in ratios of 10%, 20% and 30% in deionized water were prepared at 45°C and 1200 rpm for 1h (by Stirrer IKA). The solution was kept in cool room temperature at 4°C overnight (Badee et al, 2012; Baranauskiene et al, 2007). Then, 2.5% spearmint oil was added to an aqueous and homogenized (15000 rpm for 10 min) solution with an Ultra Turrax (model T25 digital, IKA Co, Germany) (Badee et al, 2012; Baranauskiene et al, 2007; Baranauskiene&Venskutonis, 2009; Frascareli et al, 2012). Then sonificasion (model ,HD3200, BANDELINE Co, Germany) for 1 minute by amplitude control 100%, frequency 20 kHz at 45 °C. The emulsion was spray dried in a BUCHI B-190 spray dryer (Badee et al, 2012; Baranauskiene et al, 2007; Baranauskiene&Venskutonis, 2009) where the inlet temperature was 180 °C, outlet temperature 60°C, pump speed 10 ml/min, air flow 600 l/h and pressure 4 bar. The powder was stored at -18°C until tested.Results and Discussion: The results of this research showed that during microencapsulation of spearmint oil at the fixed rate of 2.5%, wall concentration were effective in the stability of emulsions and in keeping menthol and d-limonene in microcapsule during drying and storage. By increasing wall material from 10% to 30% the most stability in emulsion was obtained and more half life and less release in microcapsules was achieved. Also, temperature plays an important role in protecting the volatile components, so that the microcapsules stored at 4°C had about half life which was 80 days more than the the samples stored at 25°C.
