microencapsulation
در نشریات گروه پزشکی-
Objective (s)
Microencapsulation is the most common technique that has been utilized to increase the stability of bioactive compounds. This study aimed to evaluate the potential of whey protein isolate (WPI) in the microencapsulation of Citrus medica essential oil (CEO) by ultrasonication method.
Materials and MethodsThe influences of core-coating ratio (10-100%) and ultrasonication power (50-150W) on the physicochemical properties of microcapsules were evaluated.
ResultsParticle diameter of the microparticles increased by increasing the core-coating ratio. PDI value increased and decreased with the increase of core ratio. The highest encapsulation efficiency (EE) (84.8%) belonged to CEO loaded microcapsule with values of US power and core-coating ratio equal 100. Mathematical modeling indicated that the type of release from microcapsule containing CEO in different simulating conditions was fake release and a combination of fake/complex release. SEM results confirmed a spherical shape-like structure. The formation of new interactions between WPI and CEO was confirmed by FT-IR analysis.
ConclusionThe results showed that the encapsulation of Citrus medica L. essential oil by biopolymers can be successful.
Keywords: Citrus medica L, Essential oil, Microencapsulation, optimization, Release kinetic -
Nowadays, there is a great interest in using yogurt sauce as a flavored dressing for salads and foods. The current study aimed to determine the possibility of producing probiotic yogurt sauce and evaluate its physicochemical, microbiological, sensory and rheological properties throughout refrigeration storage. Lactobacillus rhamnosus was encapsulated with sodium alginate and resistant starch using the emulsion method. The survival of free and microencapsulated L. rhamnosus was studied in simulated gastrointestinal conditions. Two forms (free and microencapsulated) of L. rhamnosus were added to the yogurt sauce. The samples were kept for 30 days at 4 ˚C and evaluated on interval days (1st, 10th, 20th, and 30th) for the above mentioned properties. Survival improvement was demonstrated in microencapsulated L. rhamnosus compared to free L. rhamnosus. After two hours, the free form of L. rhamnosus showed five logarithmic cycles decreasing in cell viability, while microencapsulated L. rhamnosus presented only one logarithmic cycle reduction. Similarly, on day 30 of storage, the number of viable microencapsulated L. rhamnosus cells in the probiotic yogurt sauce was 6.61 log CFU/g, while the viable count for a sample containing free L. rhamnosus was 5.00 log CFU/g. The produced probiotic yogurt sauce was considered a pseudo-plastic fluid and presented mayonnaise behaviour. Moreover, samples containing microencapsulated probiotic bacteria displayed lower post-acidification values than samples containing free bacteria. The microencapsulation of probiotic bacteria improved the sensory quality of the produced probiotic yogurt sauce. Hence, producing a probiotic yogurt sauce with desirable properties is possible.Keywords: Lactobacillus rhamnosus, Microencapsulation, Probiotic Yogurt Sauce
-
سابقه و هدف
در این مطالعه، میکروکپسولاسیون اسیدهای چرب امگا-3 به همراه باکتری پروبیوتیک لاکتوباسیلوس پلانتاروم در کوآسروای حاصل از برهمکنش الکترواستاتیک در سه فرمولاسیون بیوپلیمری مورد ارزیابی قرار گرفت.
مواد و روش ها:
به منظور بررسی تاثیر جنس دیواره از سه فرمولاسیون ژلاتین- صمغ عربی، ژلاتین- کیتوزان و صمغ عربی- کیتوزان استفاده شد، هم چنین تاثیر نسبت مواد دیواره به هسته در سه سطح 2:1، 3:1 و 4:1 و دور هموژنایزر در دو سطح 3500 و rpm 7000 بررسی شد.
یافته ها:
نتایج نشان داد که تیمار 12، بالاترین مقدار بازدهی (19 /0 ± 26 /96) را دارد که در آن مخلوط بیوپلیمر که حاوی ژلاتین-کیتوزان بود، درصد بالایی از امگا-3 را احاطه کرده در حالی که مقدار امگا-3 که در سطح کپسول حضور دارد، بسیار کم است. تیمار 6 که حاوی مواد دیواره ژلاتین و صمغ عربی بود، قابلیت بالایی برای احاطه باکتری دارد و در مقایسه با باکتری های آزاد هنگامی که در شرایط شبیه سازی شده معده قرار گرفت نرخ مرگ و میر باکتری در آن کم تر بود. به علاوه بعد از قرار گرفتن در شرایط شبیه سازی شده روده تعداد باکتری ها بعد از گذشت 120 دقیقه افزایش یافت که این امر نشان می دهد کپسول در شرایط قلیایی روده به خوبی ترکیبات خود را آزاد کرده است.
استنتاجدر نتیجه، استفاده از تکنیک کوآسرواسیون مرکب با استفاده از بیوپلیمرهای ژلاتین ماهی، کیتوزان و صمغ عربی به عنوان مواد دیواره، می تواند کپسول های حاوی امگا-3 و باکتری لاکتوباسیلوس پلانتاروم در اندازه های میکرومتری تولید کند و می تواند نقش محافظتی برای جلوگیری از اکسیداسیون این ترکیبات داشته باشد.
کلید واژگان: میکروکپسولاسیون، اسیدهای چرب امگا 3، لاکتوباسیلوس پلانتاروم، روش کواسرواسیونMicroencapsulation of Fish Oil Omega-3 Fatty Acids and Lactiplantibacillus plantarum by CoacervationBackground and purposeIn the present study, Micro-capsulated fish oil omega-3 fatty acids and Lactobacillus Plantarum produced by electrostatic interaction coacervation was investigated in three biopolymer formulations.
Materials and methodsThree biopolymer formulations of fish gelatin-gum Arabic, fish gelatin–chitosan, and gum Arabic-gelatin were used to study the effect of wall materials. Also, we investigated the effect of wall-to-core materials ratio at 2: 1, 3: 1, and 4: 1 and homogenizer speeds of 3500 and 7000 rpm.
ResultsThe results of the microencapsulation efficiency of omega-3 fatty acids showed that treatment 12 had the highest yield (96.26 ± 0.19). It contained a biopolymer mixture containing gelatin-chitosan which surrounded a high percentage of omega-3, while the amount of omega-3 on the surface of the capsule was very low. Also, treatment 6 containing gelatin wall materials and gum Arabic had a high ability to surround bacteria and compared to free bacteria, the bacterial mortality rate was lower when exposed to simulated gastric conditions. In addition, after being in the simulated intestinal condition, the number of bacteria increased after 120 minutes that shows the capsule has released its compounds in alkaline conditions of the intestine.
ConclusionThis study showed that using the combined coacervation technique using fish gelatin biopolymers, chitosan, and gum Arabic as wall materials, can produce omega-3 capsules and Lactobacillus Plantarum in micrometer sizes. They can play a protective role in preventing the oxidation of probiotic and omega-3 bacteria.
Keywords: microencapsulation, omega-3 fatty acids, Lactobacillus plantarum, coacervation -
سابقه و هدف
زرشک بی دانه Berberis vulgaris محصول بومی ایران حاوی ترکیبات ارزشمندی با اثرات درمانی، سلامتی بخش و تغذیه ای از جمله بربرین می باشد که بخش عمده ای از این گیاه به صورت ضایعات به هدر می رود. هدف تحقیق حاضر بهینه سازی شرایط استخراج بربرین از گیاه کامل با بیشترین میزان فعالیت آنتی اکسیدانی، ریز پوشانی عصاره به روش الحاق ترکیبی با استفاده از دو بیوپلیمر در دسترس، ژلاتین/کتیرای پرک (Astragalus rahensis) و بررسی ویژگی های فیزیکی میکروکپسول مرطوب می باشد.
مواد و روش هابهینه سازی به روش سطح پاسخ بر پایه سه فاکتور از فرآیند استخراج شامل زمان، دما و درصد حلال/آب در سه سطح با 5 نقطه مرکزی انجام و غلظت بربرین در عصاره به روش کروماتوگرافی مایع با کارآیی بالا و میزان فعالیت آنتی اکسیدانی آن آنالیز تا شرایط بهینه تعیین گردد. عصاره بهینه به روش الحاق ترکیبی از دو ترکیب ژلاتین/کتیرا با سه نسبت 1:1، 1:2 و 2:1 w/w ریز پوشانی شده و پارامترهای بازده، کارآیی، اندازه ذرات ، حلالیت و ساختار میکروسکوپی میکروکپسول های مرطوب و میزان رهایش بربرین از آنها مورد بررسی واقع شد.
یافته هاشرایط بهینه استخراج، در مدت زمان 5/0 ساعت، دمای C 9/22 و با نسبت 75% حلال/آب با مطلوبیت 88/0 تعیین شد. میانگین سطحی قطر میکروکپسول ها در محدود 31/71- 15/90 میکرون می باشد. کپسول با نسبت w/w1:2 پروتیین/پلی ساکارید دارای بیشترین بازده 1/95% و کپسول با نسبت 2:1 دارای بیشترین حلالیت 10% و میزان کارآیی در تمام نمونه ها یکسان و حدود 1±96% است.
نتیجه گیریروش الحاق ترکیبی با بکارگیری ژلاتین /کتیرا با نسبت 1:2، جهت تولید میکروکپسول مرطوب عصاره بهینه بربرین با بیشترین بازدهی و کارآیی، حلالیت کم و اندازه کمتر از 100 میکرون پیشنهاد و توصیه می گردد .
کلید واژگان: عصاره بربرین، فعالیت آنتی اکسیدانی، ریزپوشانی، میکروکپسول مرطوب، بازدهی و کارآیی، حلالیتBackground and ObjectivesBerberis vulgaris, an Iranian native plant, includes valuable compounds such as berberine with therapeutic, health-promoting and nutritional effects. However, major parts of this plant are discarded as wastes. The major aims of this study were optimization of berberine extraction conditions from the whole plant with maximum antioxidant activity, the extract microencapsulation using complex coacervation and two biopolymer gelatin/flake tragacanth (Astragalus rahensis) and analysis of the physical characteristics of the moist microcapsules.
Materials & MethodsBerberine extraction was optimized using response surface methodology based on three extraction parameters of time, temperature and solvent:water ratio at three levels and five central points. The berberine concentration was analyzed using high-performance liquid chromatography and its antioxidant activity was studied to investigate the optimized conditions. The optimum extract was microencapsulated using complex coacervation and gelatin/tragacanth with three ratios of 1:1, 2:1 and 1:2 w/w. Furthermore, yield, efficiency, particle size, solubility and the microstructural and release characteristics of the wet microcapsules were characterized.
ResultsOptimized extraction conditions with 0.88 desirability included 0.5 h, 22.9 °C and 75% solvent:water ratio. The average surface size of the microcapsules was in the range of 71.31–90.15 μm. Samples with 2:1 ratio indicateds the maximum yield 95.1 and sample with 2:1 ratio showed the maximum solubility of 10%. Efficiency in all samples were similarly 96% ±1.
ConclusionComplex coacervation using gelatin/tragacanth with a ratio of 1:2 was developed to produce wet microcapsules of the optimum extract of berberine with the highest yield and efficiency and low solubility as well as particle sizes of smaller than 100 μm.
Keywords: Berberine extract, Antioxidant activity, Microencapsulation, Wet microcapsules, Yield, Efficiency, Solubility -
BackgroundMicroencapsulation of probiotics can be used to increase their viability during the process and delivery to target areas in the gut and intestinal tract. The aim of this study was to investigate the effect of microencapsulation on viability of probiotics bacteria (Lactobacillus acidophilus and Bifidobactrium animalis subs lactis) in bile salt solution and simulated gastrointestinal juice conditions.MethodsFirst, 1 gram of probiotic bacteria was mixed in 100 ml of MRS broth and incubated at 37°C for 24 h until bacteria were activated. Microencapsulation of probiotics with sodium alginate/resistant starch and sodium alginate/chitosan were done by extrusion method. The number of viable bacteria was evaluated in bile salt solution (0.6%, w/v) and simulated gastric juice (0.08 mol/L HCl solution contained 0.2% NaCL and pH: 1.55 without pepsin), followed by incubation in simulated intestinal juice (0.05 mol/L KH2PO4 solution with 0.6 % bile salts and pH: 7.43).ResultsThe microencapsulation could successfully and significantly protect probiotic bacteria against adverse condition of simulated human gastro-intestinal condition. Microcapsules containing sodium alginate/resistant starch had the highest survival rate at the end of the incubation time in bile salt solution (6.3±0.2 × 106 and 4.6±0.3 × 107 for Lactobacillus acidophilus and Bifidobacterium animalis, respectively) and simulated gastrointestinal condition (4.5±0.4 × 107 and 1.7±0.2 × 106 for Lactobacillus acidophilus and Bifidobacterium animalis, respectively).ConclusionGenerally, the microencapsulation process improved the survival of probiotic bacteria under simulated gastrointestinal conditions and bile salts solution and in this case, sodium alginate / resistant starch coating was more effective than sodium alginate/ chitosan.Keywords: Probiotic bacteria, Microencapsulation, Sodium Alginate, Chitosan, Resistant starch, Gastrointestinal juice
-
Background
Probiotic products with valuable nutritional and therapeutic properties have attracted great attention in the fields of industry, nutrition, and medicine.
ObjectivesThe present study aimed to investigate the survival of Lactobacillus plantarum probiotic bacteria in capsulated and non-capsulated forms in malt products during storage. We also evaluated the pH, brix, sugar content, and organoleptic properties of the three products, a control malt (non-probiotic extract), an extract containing the probiotic bacteria without capsules, and an extract containing encapsulated probiotic bacteria.
MethodsThe probiotic strain of L. plantarum was inoculated into a barley malt extract in free and encapsulated forms. Bacterial microencapsulation was performed using the extrusion technique with sodium alginate. In addition, bacterial viability was determined using the mixed culture method in MRS agar medium at the temperature of 37°C for 48 hours. Data analysis was performed using one-way analysis of variance (ANOVA) in the Minitab 16 software.
ResultsThe count of L. plantarum in the non-capsulated form did not change significantly although it increased in the capsulated form. No significant changes were observed in the sugar content, pH, and brix during the storage of the three products. Moreover, the sensory acceptance of malt with capsulated bacteria was higher compared to the other samples.
ConclusionsAccording to the results, the probiotic strain of L. plantarum in the free and microencapsulated forms was maintained in the barley malt extract for two months of storage at the temperature of 4°C. Therefore, it seems that barley malt extract may be a favorable environment for the preservation of probiotic L. plantarum.
Keywords: Functional Food, Lactobacillus plantarum, Microencapsulation, Probiotic, Malt -
مجله دانشگاه علوم پزشکی شهید صدوقی یزد، سال بیست و هشتم شماره 4 (پیاپی 164، تیر 1399)، صص 2533 -2546مقدمه
در سال های اخیر توجه به مصرف محصولات غذایی و دارویی پروبیوتیک با توجه به خواص سلامت بخشی آن ها رو به افزایش بوده است. همواره نگهداری و زنده مانی این باکتری ها چه در محصولات و چه طی عبور از دستگاه گوارش مورد بررسی و یکی از عوامل چالشی بوده است. روش خشک کردن یکی از گزینه های مهم و کاربردی برای پایدار نمودن و استفاده آسان و سریع از سویه های میکروبی از جمله سویه های پروبیوتیک می باشد. در بین روش های مختلفی که برای ریزپوشانی وجود دارد؛ روش خشک کردن افشانی یکی از روش های مهم خشک کردن با قابلیت استفاده در حجم و اندازه صنعتی می باشد. بهینه نمودن پارامترهای تاثیرگذار بر روی کشت و جداسازی باکتری های پروبیوتیک، فاکتورهای خشک کن افشانی و انتخاب مواد مناسب برای دیواره ریزپوشانه ها از مهم ترین و پرچالش ترین موارد در بهینه سازی استفاده از این روش در مقیاس صنعتی می باشد. در این مقاله مروری عوامل موثر بر زنده مانی و مقاومت باکتری در مرحله قبل از ورود به خشک کن افشانی و عوامل موثر بر زنده مانی باکتری های پروبیوتیک طی مرحله خشک کردن افشانی بحث شده است. همچنین معیارهای مهم انتخاب مواد دیواره ریزپوشانه و آزمون هایی که اغلب بر روی ریزپوشانه های پروبیوتیک حاصل از خشک کن افشانی انجام می گردد؛ مورد بررسی قرار گرفته است.
کلید واژگان: پروبیوتیک، ریزپوشانی، خشک کن افشانی، ماده دیواره، آزمون های آنالیزیJournal of Shaeed Sdoughi University of Medical Sciences Yazd, Volume:28 Issue: 4, 2020, PP 2533 -2546IntroductionIn the recent years, attention to the use of probiotic drugs and probiotic food products, due to probiotic’s functional and health properties has been increased. The storage and the viability of the probiotics in the products and passing through the gastrointestinal tract was always a big challenge. Drying is one of the functional and important choices that can be used for stabilizing microbial species and makes the bacterial usage easy. Among different microencapsulation methods, spray drying is one of the important drying methods that can be used in industrial scale and size. Optimizing the effective parameters on the cultivation and separation of probiotic bacteria, the most important and challenging parameters of spray drying that have influence on probiotic products, and choose of the best wall materials for the cores, are the most important and challenging factors that are necessary for optimizing the microencapsulation in industrial scale. In this review article, the factors affecting the survival and resistance of bacteria in the stage before entering the spray dryer and the factors affecting the survival of probiotic bacteria during the drying stage are discussed. In addition, the important criteria for selecting microfiber wall materials and the tests that are often performed on probiotic microfiber resulting from spray drying have been examined.
Keywords: Probiotic, Microencapsulation, Spray-Drying, Wall Material, Analytical Tests -
Amoxicillin (α-amino-p-hydroxybenzyl-penicillin) is a semi-synthetic, orally absorbed and widely prescribed β-lactam antibiotic. It is now widely used for eradication of gastric Helicobacter pylori infection combined with a second antibiotic and an acid‐suppressing agent despite its short elimination half-life of one hour. The purpose of this study was to develop and evaluate amoxicillin loaded carbopol 934P mucoadhesive microcapsules for sustained drug release at the gastric mucosa to prolong the residence time of dosage form in the stomach and to achieve controlled drug release for more effective H. pylori eradication. Amoxicillin mucoadhesive microcapsules were formulated by ion gelation technique using 32 factorial designs. A 32 full factorial design was used to derive the statistical equation, ANOVA analysis, contour plots and 3D response surface plots. FT- IR (4000 cm-1- 450 cm-1) analysis of amoxicillin and with polymers was performed by using potassium bromide pellet method. Different polymer ratios of carbopol 934P and sodium alginate were used to formulate by nine formulations (F1 to F9) amoxicillin mucoadhesive microcapsules. The prepared formulations were characterized by determining their percentage of yield, particle size, percentage of entrapment efficiency, swelling index, percentage of mucoadhesion and percentage of drug release. Amoxicillin and used polymers are found to be compatible with no interaction reported by FTIR analysis. The optimized formulation (F9) exhibited a high drug entrapment efficiency of 96.04±0.03%, particle size of 847.2518±0.06 μm, yield of 98.86±0.01%, swelling index of 120.09±0.06%, and mucoadhesion of 67.00±0.02 after 8 h. A successful sustained drug release was achieved for more than 14 h. In-vitro dissolution test for optimized formulation (F9) demonstrated a slower release behavior in 0.1N hydrochloric acid followed by linear release profile in pH 7.4 phosphate buffer. The drug-to-polymer-to-polymer ratio had a more significant effect on the dependent variables. The release kinetic study of optimized formulation (F9) displayed a good fitting with zero order behavior and Korsmeyer-Peppas model has confirmed a non-Fickian release. The developed mucoadhesive amoxicillin microcapsules were observed to have adhered strongly with gastric mucosa with approximately 14 h of prolonged stay expecting improved bioavailability and reduced dosing frequency and subsequently improving patient’s compliance. The concentration of carbopol 934P and sodium alginate had highly significant effects on depended variables. The present study concludes that amoxicillin mucoadhesive microcapsules can be effectively used for the more effective treatment of H. pylori infection.Keywords: Amoxicillin, ANOVA analysis, Helicobacter pylori, Ion gelation technique, Microencapsulation, Mucoadhesive drug delivery
-
Many herbs and spices have been recommended traditionally as galactagogues and several commercial formulations prepared using herbs. Due to the presence of various compounds such as polyphenols, flavonoids, isoflavones and terpenes, bitter and stringent taste is elicited that make the consumption of these herbal preparations unpleasant. Moreover, these compounds are unstable when exposed to environmental conditions. In this regard, different approaches are used for taste masking such as microencapsulation. In the present study, microcapsules containing galactagogue herbs extract were developed through emulsification/external gelation and Box-Behnken design was used to investigate the effects of independent variables (sodium alginate: 1-1.5%, calcium chloride: 0.2-1% and extract concentrations: 1-5%) on encapsulation efficiency (EE%). Following evaluation of the model, the optimum condition of encapsulation process was selected as 1.49% sodium alginate, 0.84 CaCl2 and 1.58% extract with EE% of 77.97%. Microcapsules had an acceptable spherical morphology and the results of Fourier transform-infrared spectroscopy (FTIR) revealed the presence of the extract within the microcapsules. The mean diameters of the uncoated and chitosan-coated microcapsules were 52 and 123 μm and encapsulation yield was 50.21 and 69.7%, respectively. The polydispersity index of 0.45 and 0.48 were an indicative of polydisperse nature of the microcapsules. The loss of flavonoids in microcapsules stored at two different temperatures was insignificant. The in vitro release in simulated gastric fluid (SGF; pH 1.2) and simulated intestinal fluid (SIF; pH 7.4) were 48.1% and 80.11%, respectively during 24 h. The prepared extract-loaded microcapsules have potential to be used in matrices with neutral pH.Keywords: Galactagogues, Herbal extract, Microencapsulation, Sodium alginate, Chitosan, External gelation
-
Background and ObjectivesProbiotics are live microorganisms that, when administered in an adequate amount, confer a health benefit on the host through the gut. Saccharomyces cerevisiae is a widespread yeast found in nature. This microorganism has been used as a probiotic agent in recent years. In this study, the effect of microencapsulation on survival rate of S. cerevisiae var. boulardii in the simulated gastrointestinal tract medium and the impact of microencapsulated S. cerevisiae var. boulardii on some serum biochemical factors in a rat model was evaluated.Materials and Methods30 male wistar rats were divided into three groups (control, rats receiving microencapsulated S. cerevisiae var. boulardii, and rats receiving S. cerevisiae var. boulardii alone). The probiotic was gavaged at a dosage of 2 gr/kg BW for 8 weeks. Blood was collected from rats at the end of the treatment period and biochemical factors were measured using Mancompany kits.ResultsThe results showed a significant increase in viability of microencapsulated S. cerevisiae var. boulardii in comparison with free S. cerevisiae var. boulardii (p<0.05). Weight of rats in probiotic treated groups was significantly higher in comparison with the control group (p<0.05). Moreover, probiotic treatment reduced mean levels of triglycerides, cholesterol, free blood sugar and liver enzymes in rats.ConclusionMicroencapsulation could increase the survival rate of yeast probiotics in the gastrointestinal tract; however, more studies are needed for better understanding of the exact effect of microencapsulation on probiotics’ function.Keywords: Saccharomyces cerevisiae var. boulardii, Probiotic, Microencapsulation, Blood biochemical factors
-
The present study was targeted toward the investigation of the survival of probiotic strains, namely Lactobacillus acidophilus (LAFTI-L10) and Bifidobacterium lactis (LAFTI-B94), in both microencapsulated and free forms and their effects on physicochemical and sensory properties, stability, and microstructures of Doogh during storage for 45 days in a cold room at a temperature of 5±1°C. The statistical analysis of the results showed that the number of L. acidophilus and B. lactis in free forms decreased about 1.1 and 2.2 log cycles, respectively. However, the number of the microencapsulated forms remained relatively constant during the storage period. Both free and microencapsulated forms were successful in keeping the counts of L. acidophilus and B. lactis in Doogh high enough for the therapeutic minimum (106-107 cfu/g) after 45 days. Nonetheless, the number of microencapsulated probiotics was higher than that of the free cells (P<0.05). The acidity, pH, and stability were significantly different between the samples (P<0.01). The microstructure of the samples was affected by the microencapsulation of bacteria because the sample distribution of the clusters and particles was more regular in the samples containing microencapsulated probiotics than in those containing free forms. According to the results of sensory evaluations, probiotics not only exerted no adverse effects on the physicochemical and sensory properties of Doogh but also improved the stability, microstructure, and flavor of this drink. Therefore, Doogh can be considered an effective food carrier for the delivery of probiotic organisms.Keywords: Alginate, doogh, microencapsulation, probiotic
-
Essential oil of Citrus family plant is known to have repellent effect against mosquito. Unfortunately, due to its high volatility effect, its repellency effect was compromised. The incorporation of essential oil in a microencapsulation formulation has been shown to help improve the stability and potency of the repellent. In this study, Citrus grandis peel oil (CGPO) was encapsulated by using the interfacial precipitation chemistry technique. The microencapsulated CGPO was then formulated into lotion form to produce topical repellent formulation. This study includes the characterization of microcapsules with regards to the morphology, size distribution, zeta potential, Fourier Transmission Infrared spectrophotometer (FTIR) and Thermogravity analysis (TGA). The effectiveness of the microencapsulated CGPO-lotion formulation against mosquitoes was evaluated in the laboratory setting. Results indicated that CGPO have been successfully encapsulated with 6.5 µm in diameter and zeta potential values, -47.9 mV. The FTIR analysis spectrum indicated the presence of interaction between the wall materials in microcapsules. The TGA analysis demonstrated that microencapsulation improved the thermal stability of CGPO. Repellency assay revealed that microencapsulated CGPO- based formulation possessed excellent effect compared with pure CGPO. In conclusion, CGPO was successfully encapsulated and the microencapsulation aid to improve the repellency effect of CGPO against mosquito bites.Keywords: Microencapsulation, essential oil, DEET, Citrus grandis, Aedes aegypti
-
Probiotics are live microorganisms, which transit the gastrointestinal tract and their benefits to the health can be achieved through the consumption of dairy products. In this study, the survival and effect of the probiotic bacteria (Lactobacillus casei) in the free and capsulated form in yogurt were aimed to investigate. Two types of yogurt were prepared by free and induced sodium alginate with 2% starch encapsulated Lactobacillus casei. The bacterial survival, acidity and sensory attributes were analyzed during storage for 20 days at the refrigerated condition (4˚C). Titration of acidity in yogurt with free L.casei cells was higher compared to yogurt containing encapsulated L.casei cells. The viable cell count of L.casei in free form for yogurt production was 2.3×108 CFU/ml at inoculation time and 107CFU/g after incubation at 42˚C to reach pH 4.5. When L.casei was encapsulated in sodium alginate beads, the probiotic survival raised at a rate of 1.05 log CFU/g during the same period of storage due to protection by microencapsulation. The results of sensory indices and eventually total score for each sample confirmed the lack of tangible impact by adding encapsulated bacteria in taste, appearance, oral and non-oral tissues. Final scores of probiotic yogurt samples containing free and encapsulated L.casei were not statistically different (p>0.05). The results indicated that encapsulation with sodium alginate can significantly increase the survival rate of probiotic bacteria in yogurt compared to probiotic yogurt over an extended shelf life.Keywords: Lactobacillus casei, Probiotic, Survival, Sodium alginate, Microencapsulation
-
BackgroundWalnut green husk (WGH) extract has been known as potential preventive and therapeutic antioxidants and antimicrobials due to its high polyphenol content. In this study, preparation of spray dried WGH extract‑loaded microcapsules by maltodextrin and its blending with two other natural biodegradable polymers, pectin, or alginate were investigated.MethodsIn this study, encapsulation effciency (EE), total phenol content (Folin–Ciocalteu reagent method), antioxidant (DPPH scavenging assay) and antimicrobial activities (agar well diffusion method) structural (SEM and FTIR studies), and release properties of WGH extract‑loaded microcapsules
were investigated.ResultsHigh retention of phenolic content in microcapsules indicated the
successful encapsulation of WGH extract. Addition of biopolymers to maltodextrin matrix has a positive effect on EE and other properties of microcapsules. The microcapsules prepared with mixture of maltodextrin and pectin had higher EE (79.35 ± 0.87%) and total phenolic (TP) content (56.83 ± 1.04 mg gallic acid equivalents [GAE]/100 g) in comparison to maltodextrin and alginate mixture (EE: 75.21 ± 0.24%, TP content: 54.33 ± 1.53 mg GAE/100 g) and maltodextrin only matrix (EE: 72.50 ± 1.00%, TP content: 50.67 ± 1.35 mg GAE/100 g). Extract‑loaded microcapsules also showed nearly spherical structure, good antioxidant (with the percentage DPPH inhibition ranged from 75.17 ± 1.42% to 80.87 ± 2.29%), and antimicrobial properties (with mean inhibition diameter zone ranged from 7.76 ± 0.86 mm to 11.53 ± 0.45 mm). Fourier transform
infrared analyses suggested the presence of extract on microcapsules. The in vitro extract release from microcapsules followed an anomalous non‑Fickian diffusion mechanism with almost complete
release.ConclusionsWGH extract microcapsules can be used as novel and economic bioactive phytochemical and therapeutic agents to prevent oxidation and microbial activity.Keywords: Antioxidants, Juglans, microencapsulation, polyphenols -
مقدمهباکتری بیفیدوباکتریوم بیفیدوم بعنوان یک باکتری پروبیوتیک اثرات مفیدی بر سلامت انسان دارد. بتاکاروتن نیز به عنوان آنتی اکسیدان در غنی سازی بسیاری از فرآورده های غذایی بکار می رود. این ترکیبات بسیار حساس بوده و معمولا از ماندگاری کمی برخوردارند و ریزپوشانی تاثیر قابل ملاحظه ای بر افزایش ماندگاری آن ها دارد. در این بررسی اثر ریزپوشانی به روش خشک کردن انجمادی برروی زنده مانی باکتری بیفیدوباکتریوم بیفیدوم و پایداری بتاکاروتن، به صورت توام مورد بررسی قرار گرفت.مواد و روش هاابتدا امولسیون بتاکاروتن با محلول کازئینات سدیم و کاراگینان تهیه گردید و با یک سوسپانسیون غلیظ از باکتری بیفیدوباکتریوم بیفیدوم مخلوط شد. سپس نمونه ها توسط دستگاه خشک کن انجمادی آبگیری شد. در ادامه میزان زنده مانی باکتری و ماندگاری بتاکاروتن در نمونه های پوشش دار شده در زمان صفر و در طی نگهداری در دمای 4 و 25 درجه سانتی گراد به مدت یک ماه و هم چنین در شرایط شبیه سازی شده اسید معده بررسی گردید و با نمونه ریزپوشانی نشده در شرایط مشابه مقایسه شد.یافته هانتایج نشان داد ریزپوشانی اثر مثبتی بر روی زنده مانی باکتری بیفیدوباکتر و پایداری بتاکاروتن دارد. هم چنین حضور بتاکاروتن در نمونه های ریزپوشانی شده به صورت معنی داری (05/0˂P) باعث افزایش زنده مانی باکتری ریزپوشانی شده در طول زمان نگهداری شد. ریزپوشانی بر روی زنده مانی باکتری در شرایط شبیه سازی معده نیز تاثیر مثبت داشت.نتیجه گیریریزپوشانی باکتری بیفیدوباکتریوم بیفیدوم به صورت توام با بتاکاروتن به روش خشک کردن انجمادی با پوشش کازئین و کاراگینان شرایط مساعدی را برای افزایش زنده مانی باکتری و پایداری بتاکاروتن در طول ذخیره سازی و شرایط شبیه سازی شده معده ایجاد کرد.کلید واژگان: بتاکاروتن، بیفیدوباکتریوم بیفیدوم، پوشش دهی، کاراگینان، کازئینIntroductionBifidobacterium bifidum is a beneficial probiotic usually utilized as supplement in food and food products. Beta-carotene is also a food supplement with antioxidant activity. These compounds are usually susceptible and have short durability, therefore, microencapsulation improves the sustainability. In the present study, the effect of encapsulation using “freeze drying” method was investigated on survivability of Bifidobacterium bifidum and stability of beta-carotene.Materials and MethodsEmulsified beta-carotene in a solution of sodium caseinate and carrageenan were prepared and mixed with a dense suspension of Bifidobacterium bifidum. The solutions were then dehydrated with a freeze dryer device. The viability of bacterium and durability of beta-carotene in encapsulated samples were compared with non-encapsulated samples at the day zero and during storage at 4 and 25 °C for one month and also in simulated gastric acid situation.ResultsThe results showed that encapsulation could increase the viability of encapsulated Bifidobacterium bifidum and durability of beta-carotene. The presence of beta-carotene in encapsulated samples significantly (P˂0.05) increased the survivability of encapsulated bacterium during storage. Microencapsulation had also a significant positive impact (P˂ 0.05) on the survivability of bacterium in simulated gastric conditions.ConclusionMicroencapsulation of bifidobacterium bifidum and beta-carotene using casein and carrageenan could improve the survivability of bacterium and stability of beta-carotene during storage and in simulated gastric acid situation.Keywords: Beta-Carotene, Bifidobacterium bifidum, Carrageenan, Casein, Microencapsulation
-
مقدمهخشک کردن پاششی یکی از مهمترین راه های جلوگیری از اتلاف محصولات غذایی استراتژیک و افزایش طول عمر آنها می باشد. بهینه سازی شرایط عملیاتی این سامانه می تواند بستر مناسبی جهت تولید فرآورده هایی با کیفیت فیزیکوشیمایی ایده آل باشد.مواد و روش هاتاثیر سه پارامتر فرآیندی دما (160-130 درجه سانتی گراد) و سرعت جریان (4-2 مترمکعب بر ساعت) هوای ورودی و نرخ خوراک دهی (10-5 میلی لیتر بر دقیقه) جهت دستیابی به پودرهای فراسودمند ریزدرون پوشانی شده عصاره سرشار از رنگدانه فراسودمند بتالائین چغندر لبویی با روش سطح پاسخ مورد ارزیابی قرار گرفت. بازده پودرهای تولیدی، محتوای ترکیبات فنولی و فعالیت آنتی اکسیدانی عصاره بازسازی شده بهینه سازی گردید.یافته هامعادلات درجه دوم با ضرایب همبستگی بالا (9940-960/0) به خوبی می توانند شرایط بهینه جهت حصول بالاترین بازده فیزیکوشیمیایی را پیش بینی نمایند. افزایش دما و سرعت جریان هوای ورودی تاثیر معنی داری بر کاهش ترکیبات فنولی و آنتی اکسیدانی پودرهای بدست آمده داشته، در حالی که این روند سبب افزایش بازده تولیدی گشت. محتوای آنتی اکسیدانی و فنولی پودرهای ریز درون پوشانی شده با بازدهی کم در نرخ های بالاتر خوراک ورودی بهتر حفظ شدند. مشاهدات میکروسکوپی و اندازه ذرات نیز به طور بارزی یافته های بدست آمده را تایید نمودند. یافته ها نشان داد که بالاترین راندمان فیزیکی (75%)، محتوای فنولی (72/1238 میکروگرم اسید گالیک بر میلی لیتر) و درصد بازدارندگی رادیکال آزاد (77/78%) می تواند در شرایط بهینه دمای هوای ورودی 136 درجه سانتی گراد، سرعت جریان هوای ورودی 6/3 مترمکعب بر ساعت و نرخ خوراک ورودی 8/8 میلی لیتر بر دقیقه بدست آید.نتیجه گیریتولید با کیفیت پودرهای ریز درون پوشانی کننده عصاره چغندر قرمز تحتشرایط بهینه می تواند سرآغازی جهت توسعه غنی سازی فرآورده های غذایی با پودرهای بدست آمده محسوب گردد.کلید واژگان: آنتی اکسیدان، خشک کن پاششی، ریزدرون پوشانی، روش سطح پاسخ، عصاره چغندر قرمز، ویژگی های فیزیکوشیمیاییIntroductionSpray drying is one of the most important ways to prevent waste of strategic food products and their shelf life extension.Optimization of operating conditions involved in this system can be a suitable background to produce products with ideal physicochemical quality.Materials And MethodsThe effect of three operating parameters including inlet air temperature (IAT, 130-160°C), air flow rate (AFR, 2-4 m3/h) and feed flow rate (FFR, 4-10 mL/min) was investigated to attain the microencapsulated powders of red-beet extract containing functional pigment of betalain using RSM. The yield of produced powders, content of phenolic compounds and antioxidant activity of reconstituted extract were optimized.ResultsThe quadratic equations with high correlation coefficients (0.960-0.994) can well predict the optimal conditions to achieve the highest physicochemical efficiency. An increase in IAT and AFR had a significant effect on the decrease of the level of phenolic and antioxidant components of the obtained powders, while this trend led to an increase in the yield. The antioxidant and phenolic content of microencapsulated powders with low yield at higher FFRs are well maintained. The analysis of microscopy observations and particle size also confirmed the results clearly. The findings showed that the maximum physical yield (75%), phenolics content (1238.72 µg gallic acid/mL), and free-radical inhibition percentage (78.77%) can be obtained under the optimum conditions of 136.0°C IAT, 3.6 m3/h AFR, and 8.8 mL/min FFR.ConclusionProduction of high-quality powders microencapsulating red-beet extract under the optimal conditions might be a beginning to develop fortification of food products with the obtained powders.Keywords: Antioxidant, Microencapsulation, Physicochemical Properties, Red, Beet (Beta vulgaris var. conditiva Alef.) Extract, Response Surface Methodology (RSM), Spray Dryer
-
PurposeMultidrug resistance (MDR) of tumors to chemotherapeutics often leads to failure of cancer treatment. The aim of the study was to prepare novel MDR-overcoming chemotherapeutics based on doxorubicin (DOX) derivatives and to evaluate their efficacy in 2D and 3D in vitro models.MethodsTo overcome MDR, we synthesized five DOX derivatives, and then obtained non-covalent complexes with human serum albumin (HSA). Drug efficacy was evaluated for two tumor cell lines, namely human breast adenocarcinoma MCF-7 cells and DOX resistant MCF-7/ADR cells. Additionally, MCF-7 cells were entrapped in alginate-oligochitosan microcapsules, and generated tumor spheroids were used as a 3D in vitro model to study cytotoxicity of the DOX derivatives.ResultsDue to 3D structure, the tumor spheroids were more resistant to chemotherapy compared to monolayer culture. DOX covalently attached to palmitic acid through hydrazone linkage (DOX-N2H-Palm conjugate) was found to be the most promising derivative. Its accumulation levels within MCF-7/ADR cells was 4- and 10-fold higher than those of native DOX when the conjugate was added to cultivation medium without serum and to medium supplemented with 10% fetal bovine serum, respectively. Non-covalent complex of the conjugate with HSA was found to reduce the IC50 value from 32.9 µM (for free DOX-N2H-Palm) to 16.8 µM (for HSA-DOX-N2H-Palm) after 72 h incubation with MCF-7/ADR cells.ConclusionPalm-N2H-DOX conjugate was found to be the most promising DOX derivative in this research. The formation of non-covalent complex of Palm-N2H-DOX conjugate with HSA allowed improving its anti-proliferative activity against both MCF-7 and MCF-7/ADR cells.Keywords: Aantitumor drug screening assays, Microencapsulation, Multicellular spheroids, Multiple drug resistance, Serum albumin
-
سابقه و هدفبه دلیل حرارت بالای پخت نان و مرگ پروبیوتیک ها در طول پخت، تهیه نان پروبیوتیک حاوی باکتری های زنده گسترش چندانی نیافته است. در این تحقیق، برای افزایش زنده مانی پروبیوتیک ها حین پخت نان، از ریزپوشانی به روش امولسیون استفاده می شود.مواد و روش هاباکتری لاکتوباسیلوس پلانتاروم A7 با غلظت های مختلف آلژینات سدیم و نشاسته ذرت ریزپوشانی شد. ریزپوشینه ها با اجزای خمیر، مخلوط و نان تهیه شد. pH نان و تعداد باکتری های پروبیوتیک زنده پس از پخت نان تعیین شد. اندازه ذرات ریزپوشینه ای که بیشترین تعداد باکتری زنده را در نان حفظ کرده بود؛ تعیین شد. همچنین بافت نان در سه زمان 0، 24 و 48 ساعت پس از پخت، در دمای 25 درجه سانتی گراد ارزیابی گردید.یافته هاpH نان در محدوده مناسب برای زنده مانی پروبیوتیک ها و پایداری ریزپوشینه ها قرار داشت. ریزپوشانی تاثیر معنی داری در زنده مانی پروبیوتیک ها حین پخت نان، داشت (05/0p<) و تعداد باکتری های زنده را نسبت به نمونه شاهد، بین 2-1 سیکل لگاریتمی، افزایش داد. بیشترین تعداد باکتری زنده در نان، 70/5 سیکل لگاریتمی بود که تا میزان لازم برای ایجاد خواص پروبیوتیک، اختلاف کمی داشت (6 سیکل لگاریتمی). اندازه ذرات این ریزپوشینه، 34/29 ± 85/329 میکرومتر بود. همچنین وجود ریزپوشینه ها، باعث نرم تر شدن بافت نان، نسبت به نمونه شاهد گردید (05/0p<).نتیجه گیریروش امولسیون ضمن حفظ کیفیت مناسب در نان، می تواند به عنوان روشی برای افزایش زنده مانی پروبیوتیک ها در نان، مد نظر قرار گیرد.کلید واژگان: پروبیوتیک، نان، ریزپوشانی، امولسیون، آلژینات سدیمBackground And ObjectivesDue to the high temperature and destruction of probiotics during baking, production of probiotic breads containing the viable bacteria has not been fully developed. In this study, to increase the viability of probiotics during bread baking, microencapsulation by emulsion method was used.Materials And MethodsL. plantarum A7 was encapsulated by different concentrations of sodium alginate and corn starch. The microcapsules were mixed with dough ingredients, and the bread was prepared. The breads pH and viable counts of probiotic bacteria were determined after baking. The particle size of microcapsule that kept the highest number of live bacteria in the bread was measured. Also the breads texture at 0, 24 and 48 h storage (25°C) was evaluated.ResultsThe obtained pH of breads was in the proper range to viability of probiotics and stability of microcapsules. The microencapsulation had significant effect on the viability of probiotics during bread baking (pConclusionThe microencapsulation by emulsion method can be considered as an alternative to increase the viability of probiotic in bread with appropriate characteristics during storage.Keywords: Probiotic, Bread, Microencapsulation, Emulsion, Sodium alginate
-
سابقه و هدفروغن بزرک روغن غیراشباع حاوی 55% لینولنیک اسید می باشد که حساسیت بالایی به اکسیداسیون دارد. در این پژوهش ریزپوشینه کردن روغن بزرک به روش توده ای شدن مرکب (Complex coaservation) انجام و اثرات افزودن آن روی ویژگی های فیزیکوشیمیایی و حسی شیر در طول دوره نگهداری بررسی شد.مواد و روش ها30-20 درصد روغن بزرک از دانه بزرک به روش حلال سرد استخراج گردید. ژلاتین، صمغ عربی، آنزیم ترانس گلوتامیناز و لاکتوز به منظور ریزپوشینه کردن روغن به روش توده ای شدن مرکب مورد استفاده قرار گرفت. عددپراکسید، اسیدیته شیر غنی شده با روغن بزرک ریزپوشینه و نمونه شاهد با سطح معنی دار 05/0 اندازه گیری شد. آزادسازی روغن از ریزپوشینه ها در شیر غنی شده با روغن بزرک به روش کروماتوگرافی گازی به منظور بررسی خصوصیات شیمیایی انجام گرفت. اندازه گیری گرانروی و رنگ در سطح معنی دار 05/0 به منظور بررسی خصوصیات فیزیکی در طول نگهداری شیر به مدت یک هفته مورد بررسی قرار گرفت.یافته هانتایج FTIR نشان داد که در ریزپوشینه کردن روغن بزرک با ژلاتین و صمغ عربی و بکار بردن آنزیم ترانس گلوتامیناز که به منظور ایجاد اتصالات عرضی و استحکام در ریزپوشینه ها بود، پیوند شیمیایی جدیدی به وجود نیامده است. شیر حاوی روغن بزرک ریزپوشینه شده، اسیدیته بالاتری نسبت به نمونه شاهد داشته و از نظر اندیس پراکسید، در شیر حاوی روغن بزرک آزاد از شیر حاوی روغن پوشینه شده به طور معنی دار ( 5%=P) افزایش یافته و این افزایش برای شیر حاوی روغن بزرک آزاد و شیر حاوی روغن ریزپوشینه شده به ترتیب 206% و 72%meq/kg بوده است. رنگ نمونه غنی شده با روغن ریزپوشینه به علت پراکنش بیشتر پروتئین، سفیدتر بوده است. از نظر مقبولیت حسی نمونه غنی شده با روغن بزرک ریزپوشینه شده به طور معنی داری ( 5%=P) پایین تر از نمونه شاهد بود.نتیجه گیرینتایج عددپراکسید، اسیدیته و آزادسازی روغن بزرک از ریزپوشینه ها درون شیر حاکی از آن است که ریزپوشینه کردن با روش توده ای شدن مرکب راهی موثر در جلوگیری از اکسیداسیون شیر غنی شده است.کلید واژگان: روغن بزرک، لینولنیک اسید، ریزپوشینه کردن، توده ای شدن مرکب، اکسیداسیونBackground And ObjectivesFlax seed oil is unsaturated oil that contains 55% linolenic acid, is highly sensitive to oxidation. In this research, the physicochemical and sensory properties of enriched milk with encapsulated flaxseed oil were studied using complex conservation method .Materials And MethodsFlaxseed oil was extracted from flaxseed using solvent cold extraction. Gelatin, gum Arabic, lactose and transglutaminase were used as encapsulating materials. The microcapsulated flaxseed oil was added to milk. The physicochemical and sensory properties, peroxide value, and release of fortified and control sample were evaluated in the enriched milk during one week cold storage.
The results of FTIR showed that new chemical bonds were not formed in the flaxseed oil microencapsulated by gelatin, gum Arabic and transglutaminase. The milk contained microcapsulated flaxseed oil showed higher acidity than the control. During storage, a significant difference (p= 5%) in peroxide values was observed in the samples containing free flaxseed oil as compared to the samples containing microencapsulated flaxseed oil (206% meq/kg vs. 72% meq/kg, respectively). The color of sample enriched with encapsulated oil was whiter. The sensory evaluation showed that the acceptability of the samples enriched with microcapsulated flaxseed oil was significantly lower the control (p= 5%).
Microcapsulation of flaxseed oil using the complex conservation method is an effective way to prevent its oxidation in enriched milk. The sensory properties (taste and smell) of the milk enriched with encapsulated oil, however, showed a significant decrease. As a solution, the flavor agents can be used to promote sensorial quality of milk enriched with encapsulated flaxseed oil.Keywords: Flaxseed oil, Linolenic acid, Microencapsulation, Coacervation, Oxidation -
سابقه و هدفپوست سبز گردو از ضایعات کشاورزی است که به دلیل داشتن ترکیبات فنولی، می تواند به عنوان ترکیبات طبیعی با خواص بیولوژیک مطرح باشد. این تحقیق با هدف استخراج عصاره آبی پوست سبز و بررسی اثر دمای استخراج بر میزان ترکیبات فنولی و فعالیت آنتی اکسیدانی و ضدمیکروبی، همچنین اثر فرآیند ریزپوشانی کردن عصاره استخراجی به روش خشک کن پاششی در مالتودکسترین بر فعالیت بیولوژیک عصاره بررسی گردید.مواد و روش هادر این مطالعه عصاره آبی پوست سبز گردو (واریته سوزنی) در دو دمای 25 و 80 درجه سانتی گراد استخراج شد. در ادامه فرآیند ریزپوشانی کردن با مالتودکسترین 10 % به عنوان ماده پوشش دهنده در سه غلظت مختلف عصاره (mg/ml 2، 1، 5/0) با استفاده از روش خشک کن پاششی انجام شد. ترکیبات فنولی کل عصاره آزاد و ریزپوشانی شده تعیین گردید. فعالیت آنتی اکسیدانی عصاره آبی پوسته سبز گردو به روش مهار رادیکال DPPH (2و2 دی فنیل1- پیکریل و هیدرازیل) قبل و بعد از ریزپوشانی مورد بررسی قرار گرفت. همچنین فعالیت ضد میکروبی با استفاده از روش چاهک گذاری در آگار (Agar well diffusion method) بر روی باکتری های گرم مثبت استافیلوکوکوس اورئوس و باسیلوس سرئوس و باکتری های گرم منفی سالمونلا تیفی موریوم و اشرشیاکلی تعیین شد.یافته هانتایج نشان داد که اثر دمای استخراجی بر میزان ترکیبات فنولی معنی دار است (05/0 >P). نمونه های استخراج شده در دمای oC80 حاوی ترکیبات فنولی بیشتری (mg GAE/g 77/39) نسبت به نمونه های استخراج شده در دمای محیط (mg GAE/g 88/28) بودند. کارایی ریزپوشانی با افزایش میزان غلظت عصاره افزایش یافت. عصاره آزاد و ریز پوشانی شده به دست آمده در دمای oC80 در غلظت mg/ml 2 بیشترین اثر را در مهار رادیکال DPPH داشت (به ترتیب 05/85 و 05/81 %). علاوه بر این عصاره آزاد و ریزپوشانی شده در غلظت mg/ml 2 بیشترین اثر بازدارندگی را روی میکروارگانیسم های گرم مثبت نشان دادند. نتایج نشان دهنده عدم اختلاف معنی دار فعالیت ضدمیکروبی و آنتی اکسیدانی عصاره آزاد و ریزپوشانی شده پوست سبز گردو بود.نتیجه گیریپوسته سبز گردوی سوزنی با توجه به مقادیر مناسب ترکیبات فنولی می تواند به عنوان یک ترکیب آنتی اکسیدانی و ضدمیکروب طبیعی ارزان مورد استفاده قرار گیرد. لذا می توان از ریزپوشانی کردن به روش خشک کن پاششی به عنوان روشی کارآمد جهت افزایش پایداری عصاره پوست سبز گردو در برابر شرایط محیطی استفاده نمود.کلید واژگان: پوسته سبز گردو، عصاره آبی، فعالیت ضد میکروبی، فعالیت آنتی اکسیدانی، ریزپوشانی کردنBackground And ObjectivesWalnut green husk is one of agricultural residues that can be considered as natural compound with biological properties because of its phenolic compounds. In the present work, the goal is extraction of aqueous extract of green walnut skin and studying the effect of extraction temperature on the phenolic compounds and antioxidant and antimicrobial properties of extract. Meanwhile, the effects of spray dried encapsulation process of extract in maltodextrin on the biological activity of extract are investigated.Materials And MethodsIn this study, walnut green husk (Sozani variety) was extracted in two temperatures of 25 and 80 °C. Then it was encapsulated in 10% maltodextrin in three different concentrations of extract (0.5, 1 & 2 mg/ml) using spray drying method. Total phenol of the extract was evaluated before and after encapsulation. In addition, the antioxidant activity of the aqueous extract of walnut green husk was determined before and after microencapsulation by the scavenging effect on DPPH (2,2-diphenyl-1-picrylhydrazyl) radicals. Antimicrobial activity of the extract was determined by Agar well Diffusion Method against gram positive (Bacillus cereus, staphylococcus aureus) and Gram negative bacteria (Escherichia coli, Salmonella Typhimurium).ResultIt was revealed that the effect of extraction temperature on total phenolic compounds was significant (pConclusionSozani walnut green husk can be used as a cheap source of antioxidant and antimicrobial compounds due to having high amount of phenolic compounds. Therefore, microencapsulation can be used as an efficient method for increasing the stability of walnut green husk extract against the environmental conditions.Keywords: Walnut green husk, Aqueous extracts, Antimicrobial activity, Antioxidant activity, Microencapsulation
- نتایج بر اساس تاریخ انتشار مرتب شدهاند.
- کلیدواژه مورد نظر شما تنها در فیلد کلیدواژگان مقالات جستجو شدهاست. به منظور حذف نتایج غیر مرتبط، جستجو تنها در مقالات مجلاتی انجام شده که با مجله ماخذ هم موضوع هستند.
- در صورتی که میخواهید جستجو را در همه موضوعات و با شرایط دیگر تکرار کنید به صفحه جستجوی پیشرفته مجلات مراجعه کنید.