Food Technology
Farzaneh Esmaeili; Mahnaz Hashemiravan; Mohammad Reza Eshaghi; Hassan Gandomi
Abstract
[1]Introduction: Nowadays, there is a great tendency to consume functional foods, with special medicinal and extranutritional value in addition to basic nutritional properties. Foods containing probiotics and prebiotic compounds are classified in this category. Inulin is a water soluble storage polysaccharide ...
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[1]Introduction: Nowadays, there is a great tendency to consume functional foods, with special medicinal and extranutritional value in addition to basic nutritional properties. Foods containing probiotics and prebiotic compounds are classified in this category. Inulin is a water soluble storage polysaccharide and belongs to a group of non-digestible carbohydrates called fructans. Inulin is naturally present in some flowering plant species such as chicory and burdock root. The amount of inulin in these plants is in the range of 1 to 20% of the weight of the fresh plant. Pharmacological studies report that Burdock root contains significant amounts of the inulin as a prebiotic compounds, also exhibits a wide range of biological activities, specifically antioxidative, anti-inflammatory, and free radical scavenging activities. The aim of this study was to encapsulate the aqueous extract of burdock root and use it in a probiotic drink based on orange-carrot juice. Material and Method: The Burdock roots were obtained from the local medical plant market, Tehran, Iran. Orange and carrot juice were purchased from Nooshin and Tandis (Food Company, Tehran, Iran) respectively. Maltodextrin and gum Arabic were prepared from Merck, Germany. First, the plant roots were dried to 5.2% moisture and then its aqueous extract was extracted with the help of ultrasonication. Then burdock roots extracts were encapsulated by spray drying (microencapsulation) and freeze drying (nanocapsulation) using maltodextrin and gum Arabic as wall coating agents. Capsule properties including encapsulation efficiency, particle size distribution, moisture, density, structural properties, TPC and antioxidant were determined. Then the encapsulated extracts (at levels of 0.5 and 1%) and free extract were used in the formulation of probiotic orange-carrot juice and its effect on the survival of probiotic bacteria as well as physicochemical and sensory properties of the final product during 30 days in refrigerator (4±0.5 °C) were investigated. All experiments were carried out based on complete randomized design and the results represent the mean of at least three replicates. The data obtained were analyzed by the analysis of variance (ANOVA) using Minitab 16.0 statistical software. Significant differences between means were determined by Duncan’s multiple range test at a probability levels of P≤0.05. Results and Discussion: The results of encapsulation phase showed that Nanocapsules had higher efficiency and phenolic compounds content than microcapsules. The highest level of efficiency (92.75%) and phenolic compounds (0.385 mg GAE/g) and the smallest capsule particle size (14.33±0.22 µm) were observed in Nanocapsules prepared with gum Arabic. The SEM images showed that the produced capsules in terms of microstructure, had flaky/glassy and angular surfaces and did not have a regular shape. By adding different forms of the extract (free/micro/Nano) to the orange-carrot juice, it was found that its characteristics including viability of probiotics, formalin index, turbidity, viscosity and antioxidant activity were significantly enhanced during cold storage compared to the control (p<0.05). During refrigeration, turbidity, acidity and IC50 increased in all treatments, especially in the control sample, while other characteristics (including the viability of probiotic bacteria), showed a decreasing trend. Addition of different forms of burdock root extract did not have an adverse effect on the flavor and odor of the samples, so that, all treatments were acceptable. Therefore, based on the results of this study, it can be stated that encapsulated burdock root extracts, especially in the form of nanocapsulation, can be used to increase the viability of probiotics and enhancement the antioxidant activity of functional foods
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
Maryam Azizkhani; Rafat Karbakhsh Ravari
Abstract
The objective of this study was to improve the survival of lactic acid bacteria (LAB) in Tarhana soup as a non-dairy matrix. Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus thermophiles were encapsulated in electrospun nanofiber mats fabricated from corn starch (CS) and sodium alginate ...
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The objective of this study was to improve the survival of lactic acid bacteria (LAB) in Tarhana soup as a non-dairy matrix. Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus thermophiles were encapsulated in electrospun nanofiber mats fabricated from corn starch (CS) and sodium alginate (SA) and the protective effect of the nanofibers were investigated on the cells during the preparation of Tarhana and in the gastrointestinal tract. The moisture content of the control and nanofiber- loaded dried Tarhana samples was 8.75 and 8.71%, respectively; therefore, using nanofiber mats in the formulation had no significant effect
on the moisture content of the samples. A negative zeta potential value of -15.1 mV was found for LAB- loaded nanofibers. The nanofibers mats prepared from SA and CS mix showed a bead- free and clean structure with uniformity in size. The diameter size of most of the fibers ranged from 175- 338 with an average of 265 nm. Loading nanofiber mats with L. delbrueckii subsp. bulgaricus and S. thermophilus cells led to a uniform distributed beaded structure and the average diameter enhanced to approximately 763 nm. The viability of L. delbrueckii and S. thermophilus at the end of the electrospinning process was 92.82% and 95.83%, respectively, which indicating a slight loss in their population. Survival of nanoencapsulated S. thermophilus and L. delbrueckii was 93.50% and 89.16% respectively, while for free cells it was 85.3 and 76.4% that showed considerable protective effect of CS/SA fibers on the cells against dehydration of Tarhana medium. Nanofiber mats improved the stability of the cells against ordinary heat treatment used in preparing Tarhana soup. The survival rate of S. thermophilus was higher than L. delbrueckii subsp. bulgaricus and a significant difference was observed between the viability of free and nanoencapsulated bacteria. The survival of CS/SA nanoencapsulated S. thermophilus and L. delbrueckii subsp. bulgaricus was 83.25% and 80.21%, respectively, which is indicative of the significant protective effect of fibers on the cells against the heating process. The nanofibers also provided good stability for the cells in the gastrointestinal tract as 106 to 107 CFUg-1 of the cells were survived which is within the recommended level of potential probiotic dose to be effective. There was no significant difference in the color of all samples. Nanoencapsulation in CS/ SA nanofiber mats improved the protection of both LAB strains in simulated fluids of the stomach and intestine (Table 4). After continuous exposure to simulated gastrointestinal fluid, a significant loss of viable free LAB cells (higher than 4 log CFU/ml) was found while the population of S. thermophilus and L. delbrueckii subsp. bulgaricus encapsulated in CS/ SA nanofibers decreased only 0.45 and 0.37 log CFU after 120 min (p> 0.01), 0.93 and 0.80 log CFU after 180 min (p< 0.01), respectively. Tarhana soup prepared with probiotic– loaded nanofibers gained higher scores in terms of consistency, mouth feel, odor, taste, flavor, and overall acceptability attributes. Tarhana soup with nanofibers possessed much sour taste and flavor than samples prepared with free cells of probiotics. The results of the present study indicated that the protection obtained from CS/ SA capsules secured around106 to 107 CFU/g of the probiotic cells which are within the recommended level of probiotic dose to be functional in consumers’ body. Therefore, this product can be used by the consumers like vegetarians and lactose or milk peptide intolerants who do not consume dairy products but need potential fermented probiotic food.
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.
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
Elnaz Ghaem far; Seyed Mahmoud Reza Hojjati
Abstract
Introduction: Adding color to Foods can make them more appealing to consumers, to allow consumers to identify what taste to expect from a product, and to protect sensitive flavors from light. Color has always played a vital role in food selection and acceptance, and colorants are added to foods to alleviate ...
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Introduction: Adding color to Foods can make them more appealing to consumers, to allow consumers to identify what taste to expect from a product, and to protect sensitive flavors from light. Color has always played a vital role in food selection and acceptance, and colorants are added to foods to alleviate color lost during processing. Caramel color, from the palest yellow to the deepest brown, accounts for more than 80% (by weight) of all colorants added to the foods we eat and drink (Sengar, et al., 2014).Because of sensitivity of liquid colors to oxidation, light and heat and difficulties in their handling and incorporating, dried pigments have been developed. Microencapsulation is a technique to package materials in the form of micro- and nano-particles. There are different methods for encapsulation in the food industry. Freeze drying which has a long dehydration period, has been used as a simple technique in encapsulating water-soluble essential oils and natural aromas or drugs (Khazaei, et al., 2014). In this work, in addition to liquid caramel color production, encapsulation of liquid color with freeze drying technique through wall materials of maltodextrin and Arabic gum were carried out. The stability of microencapsulated color was then evaluated.
Materials and Methods: Rish baba grape and Kabkab date syrup were obtained from local market. Ammonium chloride, citric acid, sodium hydroxide, tween 80, Arabic gum were purchased from Merck (Germany). Glycine and maltodextrin were obtained from Sigma-Aldrich (USA) and Dextrose Company (Iran), respectively. In this study, the effect of factors such as type of catalyst (ammonium chloride-glycine), concentration of catalyst (0.5-2 molar), the pH of reaction (4-5), reaction time (60-120 minutes) on liquid color intensity of caramel produced from two natural sources of date and grape were investigated based on fractional factorial experimental design. For production of liquid caramel color, grape/date syrup was heated while being stirred to 65ᵒ C. Catalysts were then added to syrup and heated to 110ᵒC. water was added to reaction product and centrifuged. The solvent was removed by rotary evaporator (IKA HB 10, Germany).The resulting caramel color was stored under refrigeration at 4ᵒ C. In order to produce powder of caramel color, wall materials including Arabic gum and maltodextrin were dissolved in distilled water at ambient temperature to obtain 20% total solids concentration and stirred for 30 minutes at 60ᵒC. The mixture of liquid caramel color, tween80, and wall material solution was mixed in a ratio (w/w) of 1:4 (liquid caramel color: wall material) and stirred for 15 minutes. The mixture was then dried in a freeze dryer (ALPHA 1-2 LD PLUS, Germany) for 24 hours. The blank sample was prepared without wall materials and freeze-dried in similar conditions with other samples in 24 hours. Dried materials were collected and stored in brown glass bottles with screwed caps at 4⁰C until analysis. The powders were characterized using TGA/DSC thermogravimetric analysis (METTLER TOLEDO, USA), scanning electron microscopy (SEM) (TESCAN vegar, Czech Republic) and X-ray diffraction (XRD) (Billerica, MA, USA) to confirm the structural and morphological aspects of powders.
Results & Discussion: The results showed that the type of catalyst had no effect on the intensity of the colors and maximum color intensity (0.174 for color produced from grape and 0.15 for color produced from date) was obtained under these conditions: 120 minutes for reaction time, pH value = 4 and catalyst concentration of 2 molar. Results of thermogravimetric analysis (TGA) and differential scanning calorimetric (DSC) indicated the increase of thermal resistance by microencapsulation process so that initial decomposition temperature for liquid form, without wall material, with Arabic gum and with maltodextrin for grape source were 114,138,162,185°C respectively and for date source were 113,131, 143, 180°C respectively. Results of Scanning electron microscope demonstrated that size of the powders were 11-55 μm. In conclusion, microencapsulation by freeze drying could be recommended as a suitable method for stabilizing caramel color.
Hassan Mirhojati; Parvin Sharayei; Reihaneh Ahmadzadeh Ghavidel
Abstract
The acidified ethanol extracts of dried barberry which have a relatively high anthocyanin content (376.28± 1.45 mg c3g/Kg dmp) were freeze dried using maltodextrin (MDX), polyvinyl-pyrrolidone (PVP) and mixture of MDX and calcium alginate (MDX-CaAlg) as a carrier and coating agents. The qualitative ...
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The acidified ethanol extracts of dried barberry which have a relatively high anthocyanin content (376.28± 1.45 mg c3g/Kg dmp) were freeze dried using maltodextrin (MDX), polyvinyl-pyrrolidone (PVP) and mixture of MDX and calcium alginate (MDX-CaAlg) as a carrier and coating agents. The qualitative attributes of the powders were characterized by their productively encapsulation efficiency, moisture content, bulk density, colour values (L*, a*, b*, C and H° ), particle size, total phenolic compounds (TPC), free radical scavenging activity of DPPH (RSA), ferric reducing-antioxidant power (FRAP) and minimized 50% of radical- scavenging activity (IC50). Scanning electron microscope was used for monitoring the structures of the powders. To determine the stability and half- life period of microencapsulated pigments, samples were stored under different storage temperatures (4◦C and 25◦C) at relative humidity 75%. Results showed that the encapsulated powder containing PVP 8% as wall material represented the best powder quality (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.
Abbas Ahmadi; Seyed Ali Mortazavi; Elnaz Milani; Reza Rezaeemokaram
Abstract
In this study, frozen yoghurt was produced as a synbiotic product. A food product containing both probiotics and prebiotics is named as synbiotic or functional food. Lactobacillus acidophilus (La-5) as a probiotic bacteria was added to frozen yoghurt in two types; free and encapsulated, and its survivability ...
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In this study, frozen yoghurt was produced as a synbiotic product. A food product containing both probiotics and prebiotics is named as synbiotic or functional food. Lactobacillus acidophilus (La-5) as a probiotic bacteria was added to frozen yoghurt in two types; free and encapsulated, and its survivability was evaluated during 60 days storage at -18 °C . Also Fructo-oligosaccharide as a prebiotic compound was used for producing frozen yoghurt in different levels (0%, 0.4% and 0.8% (w/w)). The viable cell number in free state in samples with (0%, 0.4% and 0.8% (w/w)) Fructo-oligosaccharide was 3.8×109 cfu/ml, 3.5×109 cfu/ml and 3.8×109 cfu/ml and after 60 days of storage these numbers were decrease to 2×107 cfu/ml, 2.2×107 cfu/ml and 2.2×107 cfu/ml respectively. Whereas in encapsulated state, the viable cells in samples with (0%, 0.4% and 0.8% (w/w)) Fructo-oligosaccharide these numbers was 7.5×109 cfu/ml, 8.9×109 cfu/ml and 9.8×109 cfu/ml and after 60 days, these numbers were decreased to 2.13×109 cfu/ml, 2.5×109 cfu/ml and 2.9×109 cfu/ml.The results indicated that encapsulation of L. acidophilus could significantly (p
Elnaz Milani; Hajar Naeemi; Seyed Ali Mortazavi; Arash Koocheki
Abstract
In this study, symbiotic yog-ice (rozen yogurt) was produced that was inoculated with different levels of inulin(0,2.5 amd 5%)as prebiotic compound and Lactobacillus Casei as probiotic bacteria in two types; free and encapsulated with Sodium Algint-Whey Protein Concentration for low fat yog-ice cream.The ...
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In this study, symbiotic yog-ice (rozen yogurt) was produced that was inoculated with different levels of inulin(0,2.5 amd 5%)as prebiotic compound and Lactobacillus Casei as probiotic bacteria in two types; free and encapsulated with Sodium Algint-Whey Protein Concentration for low fat yog-ice cream.The survivability of this probiotic bacteria was evaluated under simulated gastro-intestinal conditions ,during 30 days storage at -18oC. In the samples with free state of probiotic bacteria, the number of viable cells ,after 1h exposuring simulated gastric juice(pH=2,pepcine) decreased from 9.78-9.81 log cfu/ml to 6.97-7.26 log cfu/ml,at the end of 30 days storage at -18oC,while, the viable number of encapsulated state of probiotic bacteria, after 1h exposuring simulated gastric juice, decreased from 8.15-8.66 log cfu/ml to 6.80-7.09 log cfu/ml at the end of 30 days storage at -18oc.After exposuring simulated gastric juice, samples was ezposured 2.5h under simulated intestinal juice(pH=7.4,panceratin), and the results that was gained showed that, the samples containing free probiotic bacteria after 2.5h exposuring simulated intestinal juice decreased from 8.808-9.355 log cfu/ml to 5.159-5.9 log cfu/ml at the end of 30 days storage at -18oC.While, in the samples containing sodium alginate-whey protein concentration capsules, the viable number of cells decreased from 7.38-8.201 log cfu/ml to 6.151-6.672 log cfu/ml, at the end of 30 days storage at -18oC. The results indicate that there are significant differences (p
